<?xml version="1.0" encoding="utf-8" ?>

<XML>
  <JOURNAL>   
    <YEAR>2007</YEAR>
    <VOL>7</VOL>
    <NO>4</NO>
    <MOSALSAL>29</MOSALSAL>
    <PAGE_NO>108</PAGE_NO>  
    <ARTICLES>

<ARTICLE>
    <TitleF>بررسي ارتباط پلي مورفيسم ژن گيرنده استروژن آلفا با پاسخ تخمدان به تحريك تخمك گذاري در زنان تحت درمان IVF</TitleF>
    <TitleE>The relationship between estrogen receptor alpha gene polymorphism and ovarian response to ovulation induction in women under IVF treatment</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: استروژن به عنوان يكي از مهمترين هورمون‌هاي جنسي زنانه در سيكل باروري نقش مهمي داشته و فعاليت آن در بافت‌هاي هدف از طريق گيرنده‌هاي استروژن تنظيم مي‌شود. انواع مختلفي از پلي‌مورفيسم‌ ژن گيرنده استروژن آلفا در رابطه با وضعيت‌هاي متعدد پاتولوژيك شناسايي شده‌ است. در اين تحقيق فرضيه ارتباط پلي‌مورفيسم ژن گيرنده استروژن آلفا با پاسخ تخمدان به تحريك تخمك‌گذاري در زنان نابارور تحت درمان IVF مورد بررسي قرار گرفت. 
روش بررسي: انواع ژنوتيپ ژن گيرنده استروژن آلفا در 102 زن نابارور كانديداي IVF‌ شناسايي و ارتباط آن با فاكتورهاي مشخص‌كننده پاسخ تخمدان به تحريك تخمك‌گذاري مانند ميانگين تعداد فوليكول و تخمك، نسبت فوليكول به تخمك، ميزان استروژن سرم و همچنين تعداد جنين‌هاي بدست آمده سنجيده شد. در هر بيمار براي ژن گيرنده استروژن آلفا، ژنوتيپ‌هاي PP،  Ppوpp با استفاده از تكنيك PCR-RFLP مشخص گرديد و تحليل آماري با استفاده از آزمون 2 ، كروسكال واليس و من‌ويتني با نرم افزار SPSS ويرايش 13 انجام شد. 05/0p&lt; به عنوان سطح معني‌داري تلقي شد.
نتايج: براساس نتايج اين مطالعه 4/31% افراد داراي پلي‌مورفيسم pp، 2/39% پلي‌مورفيسم Pp و 4/29% داراي پلي‌مورفيسم PP بودند. درصد علل ناباروري زنانه و مردانه، ميانگين تعداد فوليكولها، تخمكها و جنينها در سه نوع پلي مورفيسم از نظر آماري تفاوت معني‌داري نداشت. 
نتيجه‌گيري: بررسي نقش ژن‌هاي مختلف در پاسخ بدن به داروهاي گوناگون (فارماكوژنتيك) اهميت زيادي در تعيين روش‌هاي درماني مناسب دارد. اين تحقيق اهميت يكي از ژن‌هاي مؤثر در پاسخ تخمدان به تحريك تخمك‌گذاري در سيكل‌هاي IVF را نشان داد؛ اما با توجه به نقش انواع فاكتورهاي آندوكرين و پاراكرين در تحريك تخمك‌گذاري و بلوغ مناسب تخمك به مطالعات بيشتري جهت يافتن اهميت ديگر ژن‌هاي مؤثر در تخمدان و همچنين بررسي جهش‌هاي ديگر در ژن گيرنده استروژن و تعيين شيوع پلي‌مورفيسم آن در جمعيت خانم‌هاي بارور نياز است.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Estrogen, as one of the most important female hormones, plays an essential role in fertility cycle and its receptors mediate estrogen actions in target tissues. Several polymer-phisms of estrogen receptor (ER) alpha gene have been associated with different pathological conditions. In this study, the hypothesis that polymorphisms in ER alpha gene in women may be associated with their ovarian response to ovulation stimulation during in-vitro fertilization (IVF) was evaluated. 
Materials &amp; Methods: The prevalence of PvuII polymorphism of ER alpha gene in 102 infertile women undergoing IVF treatment was evaluated and its relationship to the mean number of follicles and oocytes, follicles to oocytes ratios, mean serum estrogen concent-rations, the number of obtained embryos and pregnancy rates was determined. In each patient PP, Pp, or pp genotypes were identified by using PCR-RLFP technique. Statistical analysis was done through χ&#178;, Kruskal Wallis and Mann-Whitney by using SPSS software, version 13. P-values smaller than 0.05 were considered significant.     
Results: Based on the results of the study, 31.4% of the patients showed pp, 39.2% Pp and 29.4% PP genotypes. The percentages of male and female infertility etiologies, mean number of follicles, oocytes, and embryos in all three groups had no significant differences. 
Conclusion: Investigating the role of different genes in response to different medications (Pharmacogenetics) is very important in choosing proper treatment methods. This study indi-cated the importance of one of the genes effective in ovarian response to ovulation induction in IVF treatments, but noticing the role of different endocrine and paracrine factors in ovulation induction and proper oocyte maturation, further studies are needed to find the importance of other effective genes in ovaries and to determine other ER mutations and prevalence of ER polymorphism in the fertile women&#39;s population.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>315</FPAGE>
            <TPAGE>324</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Mohammad Hasan</Name>
<MidName>MH</MidName>
<Family>Sheikhha</Family>
<NameE>محمد حسن</NameE>
<MidNameE></MidNameE>
<FamilyE>شیخها</FamilyE>
<Organizations>
<Organization>Department of Genetics, Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Department of Genetics, Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>sheikhha@yahoo.com</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Seyyed Mehdi</Name>
<MidName>SM</MidName>
<Family>Kalantar</Family>
<NameE>سید مهدی</NameE>
<MidNameE></MidNameE>
<FamilyE>کلانتر</FamilyE>
<Organizations>
<Organization>Department of Genetics, Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Department of Genetics, Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Abbas</Name>
<MidName>A</MidName>
<Family>Aflatoonian</Family>
<NameE>عباس</NameE>
<MidNameE></MidNameE>
<FamilyE>افلاطونیان</FamilyE>
<Organizations>
<Organization>Department of Obstet . and Gynecol Research and Clinical Center for Infertility, Faculty of Medicine, Yazd Shahid Sadooghi University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Department of Obstet . and Gynecol Research and Clinical Center for Infertility, Faculty of Medicine, Yazd Shahid Sadooghi University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Estrogen receptor gene</KeyText></KEYWORD><KEYWORD><KeyText>Gene polymorphism</KeyText></KEYWORD><KEYWORD><KeyText>Infertility</KeyText></KEYWORD><KEYWORD><KeyText>IVF</KeyText></KEYWORD><KEYWORD><KeyText>Ovulation induction</KeyText></KEYWORD><KEYWORD><KeyText>Oocyte</KeyText></KEYWORD><KEYWORD><KeyText>Embryo</KeyText></KEYWORD><KEYWORD><KeyText>Embryo transfer</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>252.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Berek JS. Novak’s Gynecology. 13th Edition, Philadel-phia: Lippincott Williams &amp; Wilkins. 2002;pp:973-1065.##Stephen EH, Chandra A. Declining estimates of infer-tility in the United States: 1982-2002. Fertile Steril. 2006;86(3):516-523.##Nojomi M. Epidemiology of infertility in the west of Tehran in 2000. J Am Med Women’s Assoc. 2002;57 (4):219.##پارسا نژاد محمد ابراهیم، البرزی سعید. بررسی جنبه‌های اپیدمیولوژیک و اتیولوژیک ناباروری در شیراز، مجله دانشگاه علوم پزشکی و خدمات بهداشتی درمانی شهید صدوقی یزد، ضمیمه شماره 1، سال ششم، تابستان 1377، صفحه 58.##افلاطونیان عباس، سیدحسنی سید محمد. بررسی جنبه‌های اپیدمیولوژیک و اتیولوژیک ناباروری در یزد. طرح تحقیقاتی، مرکز تحقیقاتی درمانی ناباروری، دانشگاه علوم پزشکی شهید صدوقی یزد، 1383، صفحه54.##Meldrum DR. Female reproductive aging ovarian and uterine factors. Fertil. Sterli. 1993;59:1-5##Rebar RW. Premature ovarian failure. In: Lobe RA., Kelsey R., Marcus R, editor. In Biology and pathology. Academic Press. San Diego. 2000;pp:255.##Kovas P., Matyas SZ., Boda K., Kaal SG. The effect of endometrial thickness on IVF/ICSI outcome, Hum. Reprod. 2003;18,11;2337-41.##Duffy DM, Chaffin CL, Stouffeo RL. Expression of estrogen receptor alpha &amp; beta in the rhesus monkey corpus luteum during the menstrual cycle: regulation by luteinizing hormone &amp; progesterone. Endocrinol. 2000;141;1711-17.##Chaffine CL. Estrogen receptor a and b polymor-phism: Is there any an association with bone mineral density, plasma lipids, &amp; response to postmenopausal hormone therapy? Menopause. 2006; 13(3):451-61.##Couse JF, Korach KS. Estrogen receptor null mice: what have we learned and where will they lead us? Endocrine. 1999;20(3):358-417.##Ma WG, Song H, Das SK, Paria BC, Dey SK. Estrogen is a critical determinant that specifies the duration of the window of uterine receptivity for implantation. Proc Natl Acad Sci U S A. 2003;100(5): 2963-2968.##Frazier ME., Johnson GM, Thomassen DG, Oliver CE, Patrinos A. Realizing the Potential of the Genome Revolution: The Genomes to Life Program. Science. 2003;300:290-3.##Monastero R, Cefalu AB, Camarda C, Noto D, Camar-da LK, Caldarella R, et al. Association of estrogen receptor alpha gene with Alzheimer&#39;s disease: a case-control study. J Alzheimers Dis. 2006;9(3):273-278.##Porrello E, Monti MC, Sinforiani E, Cairati M, Guaita A, Montomoli C, et al. Estrogen receptor alpha and APOE epsilon4 polymorphisms interact to increase risk for sporadic AD in Italian females. Eur J Neurol. 2006; 13(6):639-644.##Greendale GA, Chu J, Ferrell R, Randolph JF Jr, Johnston JM, Sowers MR. The association of bone mineral density with estrogen receptor gene polymer-phisms. Am J Med. 2006;119(9 Suppl 1):S79-86.##Dijkstra A, Howard TD, Vonk JM, Ampleford EJ, Lange LA, Bleecker ER, et al. Estrogen receptor 1 polymorphisms are associated with airway hyper-esponsiveness and lung function decline, particularly in female subjects with asthma. J Allergy Clin Immunol. 2006;117(3):604-611.##Lussana F, Faioni EM, Mavilia C, Bucciarelli P, Bran-di ML, Cattaneo M. Association of estrogen receptor-alpha gene polymorphisms with venous thrombosis. Haematologica. 2006;91(2):279-280.##Almeida S, Hutz MH. Estrogen receptor 1 gene poly-merphisms and coronary artery disease in the Brazilian population. Braz J Med Biol Res. 2006;39(4):447-454.##Luisi S, Galleri L, Marini F, Ambrosini G, Brandi ML, Petraglia F. Estrogen receptor gene polymer-phisms are associated with recurrence of endometrio-sis. Fertil Steril. 2006;85(3):764-766.##Kang S, Roh JW, Kim JW. Single nucleotide poly-morphism: a new risk factor for endometrial cancer? Future Oncol. 2005;1(3):323-330.##Hernandez J, Balic I, Johnson-Pais TL, Higgins BA, Torkko KC, Thompson IM, Leach RJ. Association between an estrogen receptor alpha gene polymer-phism and the risk of prostate cancer in black men. J Urol. 2006;175(2):523-527.##Zhai Y, Zhou G, Deng G, Xie W, Dong X, Zhang X, et al. Estrogen receptor alpha polymorphisms associa-ted with susceptibility to hepatocellular carcinoma in hepatitis B virus carriers. Gastroenterology. 2006;130 (7):2001-2009.##Al-Hendy A, Salama SA. Ethnic distribution of estro-gen receptor-alpha polymorphism is associated with a higher prevalence of uterine leiomyomas in black Americans. Fertil Steril. 2006;86(3):686-693.##Cai Q, Shu X O, Jin F, Dai Q, Wen W, Cheng J R, et al. Genetic polymorphism in the estrogen receptor α gene and risk of breast cancer. Cancer Epid Biom Prev. 2003;12:853-859.##Georgiou I, Konstantelli M, Syrrou M, Messinis IE, Lolis DE. Oestrogen receptor polymorphisms and ova-rian stimulation for in-vitro fertilization. Hum Reprod. 1997;12(7):1430-1433.##Sundarrajan C, Liao WX, Roy AC, Ng SC. Associa-tion of oestrogen receptor gene polymorphism with outcome of ovarian stimulation in patients undergoing IVF. Mol Hum Reprod. 1999;5(9):797-802.##Stavrou I, Zois C, Ioannidis JPA, Tsatsoulis A. Asso-ciation of polymorphisms of the estrogen receptor α gene with the age of menarche. Hum Reprod. 2002;17: 1101-05.##Kitawaki J, Obayashi H, Ishihara H, Koshiba h, Kusu-ki I, Kado N, et al. Oestrogen receptor-alpha gene polymorphism is associated with endometriosis, adeno-myosis and leiomyomata. Hum Reprod. 2001;16:51-5.##Derman SG, Seifer DB. In vitro fertilization in the older patient. Curr Women’s Health Rep. 2003;3(5): 375-83.##Popovic-Todorovic B, Loft A, Lindhard A, Bangsboll S, Andersson AM, Andersen AN. A prospective study of predictive factors of ovarian response in &#39;standard&#39; IVF/ICSI patients treated with recombinant FSH. A suggestion for a recombinant FSH dosage normogram. Hum Reprod. 2003;18(4):781-7.##Goldstein DB, Need AC, Singh R, Sisodiya SM. Potential genetic causes of heterogeneity of treatment effects. Am J Med. 2007;120(4 Suppl 1):S21-5.##Speroff L, Fritz MA. Clinical Gynecologic Endocrino-logy and Infertility, 7th Edition, Philadelphia:Lippincott Williams &amp; Wilkins. 2005;pp:1135-73.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>بررسی ارتباط پلی‌مورفیسم ژن‌های ACE، PAI-1 و فاکتور انعقادی 13 در سقط مکرر در بيماران ایرانی</TitleF>
    <TitleE>Association of ACE, PAI-1 and coagulation factor XIII gene polymorphisms with recurrent spontaneous abortion in Iranian patients</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: با توجه به شیوع حدود 5% سقط در زنان، اثرات مخرب روانی سقط بر زندگی خانوادگی افراد و اینکه علت بخشي از این سقطها مشکلات انعقادی است،در اين مطالعه پلی‌مورفیسم ژن‌هاي مهاركننده فعال‌كننده پلاسمينوژن‌ـ1 (PAI-1)، آنزيم تبديل‌كننده آنژيوتانسين (ACE) و فاكتور انعقادي 13 (FXIII) مورد بررسي قرار گرفت و ارتباط آن با سقط خودبه‌خودي در بيماران ايراني و گروه‌ كنترل سالم ارزيابي شد.
روش بررسي: 120بيمار با سابقه سقط (حداقل دو بار) به عنوان گروه بیمار و 112 خانم سالم بدون سابقة سقط به عنوان گروه كنترل مورد مطالعه قرار گرفتند. براي بررسي پلي‌مورفيسم‌هاي (4G/5G) PAI-1 و (D/I) ACE و (Val 34 Leu) FXIII، واكنش زنجيرة پلي‌مراز همراه با استفاده از آنزيم‌هاي محدودکننده (PCR-RFLP) طراحي شد. به منظور تجزيه و تحليل آماري از نرم افزار SPSS ويرايش 2/11 و از آزمون‌های t، 2 و آزمون دقيق فيشر استفاده شد. 05/0p&lt; به عنوان سطح معني‌داري در نظر گرفته شد.
نتايج: از مجموع 120 بيمار مورد بررسي 16 نفر (4/14%) براي ژن PAI-1 هموزيگوت (4G/4G) بودند كه در گروه كنترل فقط 2 نفر (2%) وضعيت مشابهي داشتند (001/0p=) و احتمال سقط مكرر در بيماران هموزيگوت 4G بيشتر بود (نسبت خطر: 2/8 و5/36-8/1CI: 95%). تعداد 38 (5/29%) بيمار و 25 نفر (6/26%) از گروه كنترل براي پلي‌مورفيسم ACE هموزيگوت (D/D) بودند كه اختلاف از نظر آماري معني‌دار نبوده است. در اين مطالعه 2 بيمار و يك كنترل براي ژنوتيپ (34leu) پلي‌مورفيسم فاكتور 13 هموزيگوت بودند.
نتيجه‌گيري: پلي‌مورفيسم (4G/4G)PAI-1 احتمالاً از طريق اختلال در سيستم انعقادي مي‌تواند باعث سقط جنين در اين افراد شود. بررسي وجود اين جهش همراه با ساير عوامل مشكوك مثل MTHFR، فاكتور 5 لايدن در بيماران مبتلا به سقط مكرر توصيه مي‌شود.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Considering the 5% prevalence of abortion in women, its devastating psycholo-gical effects on affected people’s lives and as tendency for clotting is one of the causes of recur-rent spontaneous abortion (RSA), this study was designed to compare plasminogen activator inhibitor-1 (PAI-1), angiotensin converting enzyme (ACE) and blood coagulation factor XIII (FXIII) gene polymorphisms in Iranian patients with RSA and healthy women.
Materials &amp; Methods: 120 patients with recurrent abortions (at least two) as cases and 112 healthy female controls without a history of abortion were entered into the study. In order to characterize PAI-1 (4G/5G), ACE (D/I) and FXIII (Val 34 Leu) polymorphisms, a polymerase chain reaction followed by digestion with restriction enzymes (PCR-RFLP) was designed. For the statistical analysis, SPSS software version 11.2 was used and t-test, Chi-square and Fisher’s exact tests were calculated.  P-values &lt;0.05 were considered as significant.
Results: Homozygosity for PAI-1 4G polymorphism was seen in 16 cases, (14.4%), in contrast to two persons in the control group (2%), (p = 0.001) and patients with homozygote 4G mutation were significantly more prone to RSA in contrast to others (OR: 8.2, % 95 CI: 1.8- 36.5). 38 patients, (29.5 %), and 25 people from the control group, (26.6%), were homozygote (D/D) for ACE polymorphism, depicting no statistically significant difference. Only two patients and one person from the control group had homozygosity (34leu) for FXIII polymorphism.
Conclusion: 4G/4G polymorphism for PAI-1 gene could be a thrombophilic mutation leading to abortion. Analysis of this mutation and other suspected factors such as MTHFR and FV Leiden is recommended in patients with RSA. In this study, there were no significant associations between ACE and FXIII with RSA.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>324</FPAGE>
            <TPAGE>331</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Haleh</Name>
<MidName>H</MidName>
<Family>Soltanghoraee</Family>
<NameE> هاله</NameE>
<MidNameE></MidNameE>
<FamilyE>سلطان قرایی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>soltan@avicenna.ac.ir</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Taktom</Name>
<MidName>T</MidName>
<Family>Memariani</Family>
<NameE>تکتم</NameE>
<MidNameE></MidNameE>
<FamilyE>معماریانی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mahmood</Name>
<MidName>M</MidName>
<Family>Aarabi</Family>
<NameE>محمود</NameE>
<MidNameE></MidNameE>
<FamilyE>اعرابی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Sedigheh</Name>
<MidName>S</MidName>
<Family>Hantoushzadeh</Family>
<NameE>صدیقه</NameE>
<MidNameE></MidNameE>
<FamilyE>حنطوش‌زاده</FamilyE>
<Organizations>
<Organization>Faculty of Medical Tehran University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Faculty of Medical Tehran University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Soheila</Name>
<MidName>S</MidName>
<Family>Arefi</Family>
<NameE>سهیلا </NameE>
<MidNameE></MidNameE>
<FamilyE>عارفی </FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohsen</Name>
<MidName>M</MidName>
<Family>Aarabi</Family>
<NameE>محسن</NameE>
<MidNameE></MidNameE>
<FamilyE>اعرابی</FamilyE>
<Organizations>
<Organization>Academic Unit of clinical Pharmacology ,University of Sheffield</Organization>
</Organizations>
<Universities>
<University>Academic Unit of clinical Pharmacology ,University of Sheffield</University>
</Universities>
<Countries>
<Country>United Kingdom</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Mehdi</Name>
<MidName>MM</MidName>
<Family>Akhondi</Family>
<NameE>محمدمهدی</NameE>
<MidNameE></MidNameE>
<FamilyE>آخوندی</FamilyE>
<Organizations>
<Organization>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</Organization>
</Organizations>
<Universities>
<University>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Hossein</Name>
<MidName>MH</MidName>
<Family>Modarresi</Family>
<NameE>محمدحسین </NameE>
<MidNameE></MidNameE>
<FamilyE>مدرسی </FamilyE>
<Organizations>
<Organization>Faculty of Medical Tehran University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Faculty of Medical Tehran University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Recurrent spontaneous abortion</KeyText></KEYWORD><KEYWORD><KeyText>Thrombophilia</KeyText></KEYWORD><KEYWORD><KeyText>Plasminogen activator inhibitor-1</KeyText></KEYWORD><KEYWORD><KeyText>Angiotensin converting enzyme</KeyText></KEYWORD><KEYWORD><KeyText>Coagulation factor XIII</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>253.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Buchholz T, Lohse P, Rogenhofer N, Kosian E, Pihusch R, Thaler CJ. Polymorphisms in the ACE and PAI-1 genes are associated with recurrent spontaneous miscarriages .Hum Reprod. 2003;18(11):2473-2477.##Bick RL. Recurrent miscarriage syndrome due to blood coagulation protein/platelet defects: prevalence, treat-ment and outcome results. DRW Metroplex Recurrent Miscarriage Syndrome Cooperative Group. Clin Appl Thromb Hemost. 2000;6(3):115-25.##Walker ID. Thrombophilia in pregnancy. J Clin Pathol. 2000;53:573-580.##Kupferminc MJ. Thrombophilia and pregnancy. Reprod Biol Endocrinol. 2003;1:111.##Kempf Haber M, Klimek M. Thrombophilia in preg-nancy and its influence on venous thromboembolism and recurrent miscarriages. Przegl Lek. 2005;62(3): 164-8.##Buchholz T, Thaler CJ. Inherited thrombophilia: impact on human reproduction. Am J Reprod Immunol. 2003; 49:1-13.##Abbate R, Sofi F, Gensini F, Fatini C, Sticchi E, Fedi S. Thrombophilias as risk factors for disorders of pregnancy and fetal damage. Pathophysiol Haemost Thromb. 2002;32:318-321.##Bick RL, Hoppensteadt D. Recurrent miscarriage syndrome and infertility due to blood coagulation protein/platelet defects: a review and update. Clin Appl Thromb Hemost. 2005;11(1):1-13.##Pickering W, Marriott K, Regan L. G20210A pro-thrombin gene mutation: prevalence in a recurrent miscarriage population. Clin Appl Thromb Hemost. 2001;7(1):25-8.##Lissalde-Lavigne G, Fabbro-Peray P. Factor V Leiden and prothrombin G20210A polymorphisms as risk factors for miscarriage during a first intended pregnancy: the matched case-control &#39;NOHA first&#39; study. J Thromb Haemost. 2005;3(10):2178-84.##Mtiraoui N, Borgi L, Hizem S, Nsiri B, Finan RR, Gris JC, et al. Prevalence of antiphospholipid anti-bodies, factor V G1691A (Leiden) and prothrombin G20210A mutations in early and late recurrent pregnancy loss. Eur J Obstet Gynecol Reprod Biol. 2005;119(2):164-70.##Mjoub T, Mtiraoui N, Tamim H, Hizem S, Finan RR, Nsiri B, et al. Association between adverse pregnancy outcomes and maternal factor V G1691A (Leiden) and prothrombin G20210A genotypes in women with a history of recurrent idiopathic miscarriages .Am J Hematol. 2005;80(1):12-9.##Couto E, Barini R, Zaccaria R. Association of anticar-diolipin antibody and C677T in  methylenetetrahydro-folate reductase mutation in women with recurrent spontaneous abortions: a new path to thrombophilia?. Sao Paulo Med J. 2005;123 (1):15-20.##Mtiraoui N, Zammiti W, Ghazouani L. Methylenetet-rahydrofolate reductase C677T and A1298C polymer-phism and changes in homocysteine concentrations in women with idiopathic recurrent pregnancy losses. Rep-roduction. 2006;131(2):395-401.##Glueck CJ, Wang P, Goldenberg N, Sieve L. Pregnan-cy loss, polycystic ovary syndrome, thrombophilia, hypofibrinolysis, enoxaparin, metformin. Clin Appl Thromb Hemost. 2004;10(4): 323-34.##Kotze MJ, La Grange C, Mansvelt EPG. Rapid throm-bophilia genetic test facilitates prenatal care for mother and child .SA Fam Pract. 2005;47(7):50-51.##Tsanadis G, Vartholomatos I, Korkontzelos F, Av-goustatos G, Kakosimos A, Sotiriadis A et al. Poly-cystic ovarian syndrome and thrombophilia. Hum Reprod. 2002;17(2):314-319.##Balta G, Altay C, Gurgey A. PAI-1 Gene 4G/5G Genotype: A Risk Factor for Thrombosis in Vessels of Internal Organs. Am J Hematol. 2002;71:89-93.##Charles J, Glueck MD, Michael J, Kupferminc MD. Genetic Hypofibrinolysis in Complicated Pregnancies. Obstet Gynecol. 2001;97:44-48.##Badenhop RF, Wang XL, Wilcken DE. Angiotensin-converting enzyme genotype in children and coronary events in their grandparents. Circulation. 1995;91(6): 1655-8.##Bereczky Z, Katona E, Muszbek L. Fibrin Stabiliza-tion (Factor XIII), Fibrin Structure and Thrombosis. Pathophysiol Haemost Thromb. 2003/2004;33:430-7.##Karpati L, Penke B, Katona E, Balogh I, Vamosi G, Muszbek L. A Modified, Optimized Kinetic Photo-metric Assay for the Determination of Blood Coagu-lation Factor XIII Activity in Plasma. Clin Chem. 2000;46:1946-1955.##Kohler HP. Role of blood coagulation factor XIII in vascular diseases. Swiss Med Wkly. 2001;27:131(3-4):31-4.##Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nuclea-ted cells. Nucleic Acids Res. 1988;11;16(3):1215.##Reiner AP, Schwartz SM, Frank MB, Longstreth WT Jr, Hindorff LA., Teramura G, et al . Polymorphisms of coagulation factor XIII subunit A and risk of nonfatal hemorrhagic stroke in young white women. Stroke. 2001;32(11):2580-6.##Fatini C, Gensini F, Battaglini B, Prisco D, Cellai AP, Fedi S,et al. Angiotensin-converting enzyme DD geno-type, angiotensin type 1 receptor CC genotype, and hyperhomocysteinemia increase first-trimester fetal-loss susceptibility. Blood Coagul Fibrinolysis. 2000;11 (7):657-62.##Gris JC, Neveu S, Mares P, Biron C, Hedon B, Schved JF. Plasma fibrinolytic activators and their inhibitors in women suffering from early recurrent abortion of unknown etiology. J Lab Clin Med. 1993; 122(5):606-15.##Glueck CJ, Wang P, Fontaine RN, Sieve-Smith L, Tracy T, Moore SK. Plasminogen activator inhibitor activity: an independent risk factor for the high mis-carriage rate during pregnancy in women with poly-cystic ovary syndrome. Metabolism. 1999;48(12): 1589-95.##Wiwanitkit V. Angiotensin-converting enzyme gene polymorphism: I and D alleles from some different countries. Clin Appl Thromb Hemost. 2004;10(2):179-82.##Mello G, Parretti E, Gensini F, Sticchi E, Mecacci F, Scarselli G, et al. Maternal-fetal flow, negative events, and preeclampsia: role of ACE I/D polymorphism. Hypertension. 2003; 41(4):932-7.##Barley J, Blackwood A, Carter ND, Crews DE, Cruickshank JK, Jeffery S, et al. Angiotensin conver-ting enzyme insertion/deletion polymorphism: Associa-tion with ethnic origin. J Hypertens. 1994;12:955.##Behjati R, Modarressi MH, Jeddi-Tehrani M, Dokoo-haki  P, Ghasemi J, Zarnani AH,  et al. Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion. Ann Hematol. 2006; 85(4):268-71.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>ارتباط اختلالات كروموزومي در تخمك‌‌هاي بارور نشده و هورمون‌هاي  FSHو LH در سيكل‌هاي IVF</TitleF>
    <TitleE>The relationship between chromosomal abnormalities in unfertilized oocytes and female factors in IVF cycles</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: امروزه تكنيك‌هاي كمكي توليدمثل (ART) مي‌تواند منجر به تولد نوزاد و كمك به حل مسأله ناباروري ‌گردد. به رغم بهره‌گرفتن از اين تكنيكها، در حدود 10 تا 15% از تخمكها بارور شده باقي مي‌‌مانند كه عدم موفقيت كامل لقاح (TFF) ناميده مي‌شود. اين مسأله باعث افزايش هزينه‌هاي زوج نابارور و اتلاف وقت تيم درماني ‌مي‌گردد. هدف اين مطالعه بررسي ارتباط بين اختلالات كروموزومي تخمك‌‌هاي نابارور و هورمون های زنانه FSH و LH مي‌باشد. 
روش بررسي: تخمك‌‌هاي بارورنشده پس از انجام سيكل‌هاي درماني IVF ، طبق روش Tarkowski براي مطالعات كروموزومي آماده شدند و بعد از رنگ‌آميزي با گيمسا مورد تجزيه و تحليل کروموزومی قرار گرفتند. براي سنجش هورمون های FSH و LH از تست ELISA استفاده گرديد. سپس نتايج با استفاده از آزمون 2 و ضريب همبستگي با استفاده از برنامه آماري SPSS بررسي شد. مقدار 05/0p&lt; به عنوان سطح معني‌داري در نظر گرفته شد.
نتايج: از مجموع 52 سيكل درماني تعداد 362 تخمك دريافت شد كه پس از انجام IVF تعداد 285 تخمك بارور گرديد و 77 تخمك بارور نشد. با توجه به حذف 26 عدد از تخمك‌هاي بارور شده تجزيه و تحلیل کروموزومی روي 51 تخمك انجام شد كه در 9 سيكل درماني 16 تخمك اختلال كروموزومي داشتند. بيشترين اختلالات مربوط به كروموزوم‌هاي گروه C و كمترين اختلالات مربوط به گروه G در دسته‌بندي استاندارد بود. ارتباط معني‌داري بين اختلالات كروموزومي، سطح FSH و LH (به ترتيب با ميانگين IU/L1/8 22/16 و IU/L 8/374/7)، سن و مدت زمان ناباروري بدست نيامد. 
نتيجه‌گيري: نتايج بدست آمده در اين تحقيق نشان مي‌دهد ارتباط معني‌داري بين اختلالات كروموزومي تخمك‌‌هاي نابارور و فاكتورهاي زنانه وجود ندارد. بنابراين به نظر مي‌رسد براي مشخص نمودن علت اصلي عدم موفقيت تخمكها در سيكل‌هاي ناباروري، در صورتيكه در سيكل خاصي اختلالات تخمكي يا هورمون زنانه مرتبط نباشد، ساير فاكتورهاي مرتبط از جمله عملكرد اسپرم در فرآيند لقاح بايد مدنظر قرار گيرد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Using Assisted Reproductive Techniques (ART) may result in the birth of a neonate and help solve the infertility problem. However, 10-15% of oocytes fail to fertilize and this is called a Total Fertilization Failure (TFF). This failure may impose financial burden on the infertile couples and be time consuming to IVF team. The aim of this study was to determine the relationship between chromosomal abnormalities of unfertilized eggs and female hormones, FSH and LH.
Materials &amp; Methods: Unfertilized oocytes from IVF treatment cycles were prepared by Tar-kowski method for chromosomal studies and after staining by Giemsa method, they were chro-mosomally analyzed. For hormonal evaluations of FSH and LH, ELISA was used. The results were analyzed by ANOVA and correlation coefficient calculations through using SPSS software and p-values &lt;0.05 were considered significant. 
Results: From 52 treatment cycles, 362 oocytes were left for IVF from which 285 oocytes were fertilized and 77 oocytes were unfertilized. Considering the elimination of 26 fertilized oocytes chromosomal analyses were done on 51 ova and sixteen oocytes from nine treatment cycles had chromosomal abnormalities. Most abnormalities were in the C group and the minimum were observed in the G group of the standard classification of chromosomes. There were no significant relationships between chromosomal abnormalities and FSH, LH levels (with mean values of 16.228.1IU/L and 7.743.8IU/L respectively), age and duration of infertility.
Conclusion: The results of this study showed that there were no relationships between chromo-somal abnormalities of oocytes and female factors. Therefore, it seems that for the identification of the main causes of TFF in infertility cycles, it is necessary to consider other related factors such as sperm function, when there is no oocyte or female hormone abnormalities.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>331</FPAGE>
            <TPAGE>338</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Seyyed Mehdi</Name>
<MidName>SM</MidName>
<Family>Kalantar</Family>
<NameE>سید مهدی</NameE>
<MidNameE></MidNameE>
<FamilyE>کلانتر</FamilyE>
<Organizations>
<Organization>Department of Reproduction &amp;amp; Genetics, Research &amp;amp; Clinical Center For Infertility, Yazd University of Medical Sciences &amp;amp; Health Services</Organization>
</Organizations>
<Universities>
<University>Department of Reproduction &amp; Genetics, Research &amp; Clinical Center For Infertility, Yazd University of Medical Sciences &amp; Health Services</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>smkalantar@yahoo.com</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Ali Asghar</Name>
<MidName>AA</MidName>
<Family>Pilevarian</Family>
<NameE>علی‌اصغر</NameE>
<MidNameE></MidNameE>
<FamilyE>پیله‌وریان</FamilyE>
<Organizations>
<Organization>Faculty of Sciences, Isfahan Payam Noor University</Organization>
</Organizations>
<Universities>
<University>Faculty of Sciences, Isfahan Payam Noor University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Seyyed Peyman</Name>
<MidName>SP</MidName>
<Family>Moghaddasi</Family>
<NameE>سید پیمان</NameE>
<MidNameE></MidNameE>
<FamilyE>مقدسی</FamilyE>
<Organizations>
<Organization>Faculty of Sciences, Isfahan Payam Noor University</Organization>
</Organizations>
<Universities>
<University>Faculty of Sciences, Isfahan Payam Noor University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Chromosomal abnormalities</KeyText></KEYWORD><KEYWORD><KeyText>Female hormones</KeyText></KEYWORD><KEYWORD><KeyText>Infertility</KeyText></KEYWORD><KEYWORD><KeyText>IVF</KeyText></KEYWORD><KEYWORD><KeyText>Unfertilized oocytes</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>254.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Edirisinghe WR, Murch AR, Yovich JL. Cytogenetic analysis of human oocytes and embryos in an In vitro fertilization programme. Hum Reprod. 1992;7:230-6.##Bedford JM, Kim HH. Sperm/egg binding patterns and oocytes cytology in retrospective analysis of fertili-zation failure In vitro. Hum Reprod. 1993;8:453-63.##Wall MB, Marks K, Smith TA. Cytogenetic and fluore-scent in-situ hybridization chromosomal studies on In-vitro fertilized and intracytoplasmic sperm injected failed-fertilized. University Press, Cambridge, UK. 1996;pp:235-242.##Abruzzo MA, Hassold TA. Etiology of nondisjunction in humans. Environ Mol. Mutagen 1995;25(Suppl. 26): 38-47.##Kalantar SM, Lenton EA, Barratt CLR. Sperm function tests and fertilization failure following IVF. In Human sperm acrosome reaction. Fenichel P, Parinaud J, (Editors). Colloque INSERM/John Libbey Eurotext Ltd. 1995;236:pp.439-440.##Kalantar SM, Lenton EA. Evaluating the ability of bio-logical substancesfor induction of acrosome reaction in normospermic samples. Midd East Ferti Soci J. 2000; 5:2;71-78.##Kalantar SM, Lenton EA, Brewis I, Barratt C, Moore H. Fertilization failure of IVF predictive power of SFT. Andrologia. 1998;30(4-5):180-181.##Plachot M. Oocyte- genetic aspects. In Grudzinskas J G, Yovich JL (Editors). Gametes- The Oocyte. Camb-ridge University Press, Cambridge. 1995;pp:95-107.##Nakaoka Y, Okamoto E, Miharu1 N, Ohama K. Chro-mosome analysis in human oocytes remaining unferti-lized after In-vitro insemination: effect of maternal age and fertilization rate. Hum Reprod. 1998;13:419-424.##Ma S, Robinson W, Ryan Lam, Basil Ho Yuen. Mater-nal origin of monosomy 21 derived from ICSI: Case report. Hum Reprod. 2001:16;1100-3.##Macas E, Floresheim Y, Hotz E, Imthurn B, Keller PJ, Walt H. Abnormal chromosomal arrangements in human oocytes. Hum Reprod. 1990;5:703-7.##Pellestor F, Anahory T, Hamamah S. The chromoso-mal analysis of human oocytes. An overview of estab-lished procedures. Hum Reprod Update. 2004;1-18.##Tarin JJ, Gomez E, Sampaio M. Cytogenetic analysis of human oocytes from fertile women. Hum Reprod. 1991;8:1100-3.##Kamiguchi Y, Rosenbusch B, Sterizik K, Mikamo K. Chromosome analysis of unfertilized human oocytes prepared by a gradual fixation-air human oocytes. Hum Reprod. 1993;11:2230-8.##Almeida PA, Bolton VN. The relationship between chromosomal abnormalities in the human oocytes and fertilization in vivo. Hum Reprod. 1994;9:343-6.##Sengoku K, Tamate K, Takuma N, Yoshida T, Goishi K, Ishikawa M. The chromosomal normality of unferti-lizes oocytes from patients with polycystic ovarian syndrome Hum Reprod. 1997;12(3):474-7.##Agarwal A, Said TB, Bedaiw MAy, Banerjee J, Alva-rez JG. Oxidative stress in an assisted reproductive techniques setting. Fertil Steril. 2006;86: 503-14.##Kalantar SM, Ebrahimi A, Fazli H, Soleimani M, Aflatoonian A. The chromosomal abnormality of un-fertilized oocytes in In Vitro Fertilization program. I.J. R.M. 2003;1(1):32-36.##World Health Organization. WHO Laboratory Manual for the Examination of Human Semen and Sperm-Cer-vical Mucus Interaction. 4th Edition. Cambridge. 1999.##Aflatounian A, Karimzadeh MA, Dehghani R, Kalan-tar SM, Soliman M. The role of aspiration of half ovarian follicles prior to admistration of hCG or GnRH -a for prevention of severe OHSS in ART programs. Midd. East. Fertil Soci. 2000;5(1):73-5.##Tarkowski AK. An air-drying method for chromo-some preparation from mouse eggs. Cytogenetics. 1996;5:394-400.##Mitelman F. An International System for Human Cytogentic Nomenclature. Karger. Switzerland. 1995##Bedford JM, Kim HH. Sperm/egg binding patterns and oocytes cytology in retrospective analysis of fertiliza-tion failure in vitro. Hum Reprod. 1993;8:453-63.##Tarin JJ, Gomez E, Sampaio M. Cytogenetic analysis of human oocytes from fertile women. Hum Reprod. 1991;8:1100-3.##Wall MB, Marks K, Smith TA, Gearou CM, Magg-leton-Harris AL. Cytogenetic and fluorescent in-situ hybridization chromosomal studies on in-vitro ferti-lized and intracytoplasmic sperm injected ‘failed-fertilized’ human oocyte. Hum Reprod. 1996;11(10): 2230-8.##Mozdarani H, Aghaei F. Cytogenetics analysis of failed-fertilized oocytes from Iranian infertile women after in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI) procedures. MEFSJ. 2001;6(3): 216-225.##Dyban A, De Sutter P, Verlinsky Y. Preimplantation cytogenetic analysis. In Verlinsky Y, Kuleiy AM (Edi-tors). Preimplantation Diagnosis of Genetic Disease. 1993; Wiley-Liss New York, pp.98.##Nakaoka Y, Okamoto E, Miharu N, Ohama K. Choro-mosome analysis in human oocytes remaining unferti-lizes after in-vitro insemination: effect of maternal age and fertilization rate. Hum Reprod. 1998; 13(2):419-24.##Lim AST, Ho ATN, Tsakok MFH. Chromosomes of oocytes failing in-vitro fertilization. Hum Reprod. 1995;10:2570-5.##Pellestor F, Andr&#233;o B, Arnal F, Humeau C, Demaille J. Mechanisms of non-disjunction in human female meiosis: the co-existence of two modes of malsegre-gation evidenced by the karyotyping of 1397 in-vitro unfertilized oocytes. Hum Reprod. 2002;17: 2134-45.##Smith R, Walker L, Cobo AC, Contribution of chro-mosomal abnormalities to in vitro fertilization failures. Rev Med Chil. 1998;126(5):511-9.##Zenzes MT, Casper RF. Cytogenetics of human oo-cytes, zygotes and embryos after in vitro fertilization. Hum Genet. 1992;88:367-37.##Angell R. First-meiotic-division nondisjunction in hu-man oocytes. Am J Hum Genet. 1997;61:23-32.##Pellestor F. Frequency and distribution of aneuploidy in human female gametes. Hum Genet. 1991;86:283-8.##Pellestor F, Andr&#233;o B, Arnal F, Humeau C, Demaille J. Maternal aging and chromosomal abnormalities: new data drawn from in vitro unfertilized human oocytes. Hum Genet. 2003;112:195-203.##Takehiro I, Masayuki K, Hiroyuki A, Yutaka S, Hiro-yoshi H. Growth, antrum formation and estradiol pro-duction of bovine preantral follicles cultured in a serum-free medium. Biol Reprod. 2002;67:1099-105.##Lin YH, Hwang JL, Huang LW, Mu SC, Seow KM, Chung J, et al. Combination of FSH priming and hCG priming for in-vitro maturation of human oocytes. Hum Reprod. 2003;18:1632-36.##Gras L, McBain J, Trounson A, Kola I. The incidence of chromosome aneuploidies in stimulated and unsti-mulated (natural) uninseminated human oocytes. Hum Reprod. 1992;7:1396-401.##Gomes CM, Raineki C, de Paula PR, Severino GS, Helena CVV, Anselmo-Franci JA, et al. Neonatal handling and reproductive function in female rats. J Endocrinol. 2005;184(2):435-45.##Mousset-Sim&#233;on N, Jouannet P, Le Cointre L, Cous-sieu C, Poirot C. Comparison of three in vitro culture systems for maturation of early preantral mouse ovari-an follicles. Zygote. 2005;13:167-75.##Detwiler MR, Reuben M, Lix D, Rogers E, Lin R. Two zinc finger protein, OMA-1 and OMA-2 are edun-dantly required for oocyte maturation in C elegans. Dev Cell. 2001;1:187-99.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>مطالعه تاثیر فاکتورهای رشد TGF-β2 وBMP-2 بر تمایز سلول‌های بنیادی جنینی به کاردیومیوسیت</TitleF>
    <TitleE>Studying the effects of TGF-β2 and BMP-2 growth factors on differentiation of murine embryonic stem cells into cardiomyocytes</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: تحقیقات در زمینه سلول‌های بنیادی و كاربردهاي بالقوة آنها نویدی برای درمان بسياري از بیماری‌های صعب‌العلاج از جمله آسيب‌هاي قلب فراهم نموده است. در این رابطه تمایز هدايت شده و تحت كنترل سلول‌های بنیادی به سلول‌های میوکاردی در خارج از بدن و حتي در موضع بافت آسيب‌ديده حائر اهمیت است. با توجه به نقش دو فاکتور TGF-β2 وBMP-2 از خانواده بزرگ فاكتورهاي رشد TGF-β در رشد، تمایز، مهاجرت و ساير اعمال سلولی طی تکامل جنینی، در مطالعه حاضر اثرات این دو فاکتور بر تمایز سلول‌های بنیادی جنینی به کاردیومیوسیت مورد بررسی قرار گرفت. 
روش بررسي: سلول‌های بنیادی جنینی موش نژاد 129 از رده CCB برای تولید کاردیومیوسیتها مورد مطالعه قرار گرفتند. در این روش به منظور تأثیر هرچه بیشتر فاکتورهاي فوق، کلونی سلول‌های بنیادی در گروه‌های تجربی بر روی فیبروبلاست غیرفعال كشت داده شد و به مدت 24 ساعت با محیط کشت تمایزی حاوی  ng/ml8 فاكتور TGF-β2 و ng/ml5 فاكتور BMP-2 همراه با کاهش سرم از 20% به 5/7% تغذیه شدند. سپس از این سلولها اجسام جنینی 800 سلولی در قطرات معلق و سوسپانسیون تهيه گرديد و سپس اجسام جنینی در پلیت‌های ژلاتینه کشت داده شدند. با تداوم كشت سلول‌های بنیادی به سلول‌های ضربان‌دار تمایز یافتند. به منظور تائید تأثیر فاکتورها بر تمایز سلول‌های بنیادی جنینی به کاردیومیوسیت، بیان فاکتورهای رونویسی اولیه MEF-2 وNKx2.5 و ژن‌های تخصصی سلول‌هاي قلبی MHC،ANF  و MLC-2vبا روش RT-PCR نیمه کمی و بیان پروتئین دسمین و آلفا اکتینین در کاردیومیوسیت‌‌های تمایز یافته به روش Western-blot و حضور كارديوميوسيت‌هاي تمايز يافته بوسيله رنگ‌آميزي ايمنوهيستوشيمي با آنتي‌بادي اوليه ضد دسمين بررسی شد. 
نتایج: پس از طی مراحل تمایزی، از اطراف اجسام جنینی پلیت شده سلول‌های تمایز یافته دوکی شکل ضربان‌دار در گروه‌های تجربی در مقايسه با گروه كنترل به وضوح قابل مشاهده بود. با توجه به مقایسه کمی باندهای حاصله از PCR RT- اجسام جنینی پلیت شده در محیط‌های با فاکتورهای مختلف مشاهده گرديد که فاکتور TGF-β2 از فاكتور BMP-2 و هر دو فاکتور به صورت همزمان از هر يک به تنهایی، اثر افزایشی بيشتري بر تمایز کاردیومیوسیتها از سلول‌های بنیادی جنینی دارد. این امر با اندازه‌گیری کمی باندهایRT-PCR حاصله از بیان ژن‌های تخصصی قلبی در سلول‌های کاردیومیوسیت‌های تمایز یافته نشان داده شد. همچنین در اجسام جنینی پلیت شده در محیط با هر دو فاکتور پس از تمایز، بیان دو پروتئین دسمین و آلفا اکتینین توسط  Western-blot و نیز حضور سلول‌های کاردیومیوسیت توسط نشانگذاری پروتئین دسمین با روش ایمنوهیستوشیمی تأیید شد.  
نتیجه‌گیری: نتایج اين مطالعه نشان داد که تأثیر همزمان دو فاکتور BMP-2, TGFB2 همراه با کاهش سرم در طی زمان کشت و جسم جنینی، هدايت سلول‌هاي بيماري جنيني را در جهت تمايز به كارديوسيتها افزايش مي‌دهد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Stem cell therapy seems promising for the treatment of incurable diseases such as injured myocardium. Directed in vitro differentiation of embryonic stem cells (ES) to cardiomyo-cytes is invaluable. TGFβ-2 and BMP-2, two different growth factors from the transforming growth factor-β superfamily (TGF-β), exhibit their effects on growth, immigration and different-tiation and other cellular functions during embryonic development. In this study, the effects of these factors on differentiation of ES cells into cardiomyocytes were evaluated.
Materials &amp; Methods: Murine embryonic stem cells (CCB derived from mouse strain 129) were used for cardiomyocyte differentiation. To increase the effects of the factors, ES cells were grown on inactivated fibroblasts for 24 hours in differentiating culture medium containing 8 ng/ml of TGF-β2 and 5 ng/ml of BMP-2 while decreasing serum concentration from 20% to 7.5%. Later, embryoid bodies (EB) were formed in 800-cells hanging drops and suspension from ES cells and eventually, EBs were cultured on gelatin-coated plates. After continuation of these steps, ES cells differentiated into beating cells. To determine the effects of the growth factors on ES cell differen-tiation into cardiomyocytes, expression of primary transcribing factors, MEF2, Nkx2.5, and specific cardiac genes including MHC, ANF, MLC-2v were assessed by semiquantitative RT-PCR and expression of desmin and α-actinin in differentiated cardiomyocytes was studied by western blotting and immunostaining.
Results: After completion of the differentiation process, the EBs in the experimental groups exhibited beating compared with the control group. Considering the quantitative comparison of the dectrophoretic bands of RT-PCR and PCR products of the plated EBs in different media, it was seen that TGF-2 from BMP-2 and both factors together, compared to each one alone, is more effective on differentiation of embryonic stem cells into cardiomyocytes. In addition, in plated EBs, in a medium containing both factors, the expression of desmin and -actinin were determined by western blotting and the presence of cardiomyocytes, by marking desmin, by immunohistochemical staining.
Conclusion: The results showed that the synchronized effects of both factors, while decreasing serum concentration during ES and EB cell cultures, increases differentiation of ES cells into cardiomyocytes.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>338</FPAGE>
            <TPAGE>349</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Elham</Name>
<MidName>E</MidName>
<Family>Safarpour</Family>
<NameE>الهام</NameE>
<MidNameE></MidNameE>
<FamilyE>صفرپور</FamilyE>
<Organizations>
<Organization>Department of Biology, Faculty of Sciences, Islamic Azad University, Science &amp;amp; Research Campus</Organization>
</Organizations>
<Universities>
<University>Department of Biology, Faculty of Sciences, Islamic Azad University, Science &amp; Research Campus</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Kazem</Name>
<MidName>K</MidName>
<Family>Parivar</Family>
<NameE>کاظم </NameE>
<MidNameE></MidNameE>
<FamilyE>پریور</FamilyE>
<Organizations>
<Organization>Department of Biology, Faculty of Sciences, Islamic Azad University, Science &amp;amp; Research Campus</Organization>
</Organizations>
<Universities>
<University>Department of Biology, Faculty of Sciences, Islamic Azad University, Science &amp; Research Campus</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Mehdi</Name>
<MidName>MM</MidName>
<Family>Akhondi</Family>
<NameE>محمدمهدی</NameE>
<MidNameE></MidNameE>
<FamilyE>آخوندی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mahmood</Name>
<MidName>M</MidName>
<Family>Jeddi-Tehrani</Family>
<NameE>محمود </NameE>
<MidNameE></MidNameE>
<FamilyE>جدی‌تهرانی</FamilyE>
<Organizations>
<Organization>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</Organization>
</Organizations>
<Universities>
<University>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Fazel</Name>
<MidName>F</MidName>
<Family>Shokri</Family>
<NameE>فاضل </NameE>
<MidNameE></MidNameE>
<FamilyE>شکری </FamilyE>
<Organizations>
<Organization>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</Organization>
</Organizations>
<Universities>
<University>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Amir Hassan</Name>
<MidName>AH</MidName>
<Family>Zarnani</Family>
<NameE>امیرحسن</NameE>
<MidNameE></MidNameE>
<FamilyE>زرنانی</FamilyE>
<Organizations>
<Organization>Nanobiotechnology Research Center, Avicenna Research Institute (ACECR)</Organization>
</Organizations>
<Universities>
<University>Nanobiotechnology Research Center, Avicenna Research Institute (ACECR)</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad</Name>
<MidName>M</MidName>
<Family>Keramatipour</Family>
<NameE>محمد</NameE>
<MidNameE></MidNameE>
<FamilyE>کرامتی پور</FamilyE>
<Organizations>
<Organization>Faculty of Medical Tehran University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Faculty of Medical Tehran University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Sheida</Name>
<MidName>Sh</MidName>
<Family>Salehkhou</Family>
<NameE>شیدا</NameE>
<MidNameE></MidNameE>
<FamilyE>صالح‌خو</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Leila</Name>
<MidName>L</MidName>
<Family>Eini</Family>
<NameE>لیلا</NameE>
<MidNameE></MidNameE>
<FamilyE>عینی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Reza</Name>
<MidName>MR</MidName>
<Family>Sadeghi</Family>
<NameE> محمدرضا</NameE>
<MidNameE></MidNameE>
<FamilyE>صادقی</FamilyE>
<Organizations>
<Organization>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</Organization>
</Organizations>
<Universities>
<University>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>sadeghi@avicenna.ac.ir</Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Embryonic stem cell</KeyText></KEYWORD><KEYWORD><KeyText>Differentiation</KeyText></KEYWORD><KEYWORD><KeyText>Cardiomyocyte</KeyText></KEYWORD><KEYWORD><KeyText>TGF-B2</KeyText></KEYWORD><KEYWORD><KeyText>BMP-2</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>255.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Evans MJ, Kaufman MH. Establishment in culture of pluripotential cells from mouse embryos. Nature. 1981; 292:154-156.##Doetschman TC, Eistetter H, Katz M. The in-vitro development of blastocyst-derived embryonic stem cell lines: formation of visceral yolk sac, blood islands and myocardium. J Embryol Exp Morphol. 1985;87:27-45.##Boheler KR, Czyz J, Tweedie D. Differentiation of Pluripotent Embryonic Stem Cells Into Cardiomyo-cytes. Circ Res. 2002;91:189-201.##Ullao-Montoya F, Verfaillie C, Hu W. Culture systems for pluripotent stem cells. J Biosci Bioeng. 2005;100: 12-27.##Nichols J, Davidson D, Taga T. Complementary tissue-specific expression of LIF and LIF-receptor mRNAs in early mouse embryogenesis. Mech Dev. 1996;57:123-31.##Zandstra PW, Nagy A. Stem cell bioengineering. Annu Rev Biomed Eng. 2001;3:275-305. Review.##Kumar D, Kamp TJ, Lewinter M. Embryonic stem cells: differentiation into cardiomyocytes and potential for heart repair and regeneration, Coron. Artery Dis. 2005; 16:111-6.##Wobus AM, Wallukat G, Hescheler J. Pluripotent mouse embryonic stem cells are able to differentiate into cardiomyocytes expressing chronotropic responses to adrenergic and cholinergic agents and Ca 2  channel blockers. Differentiation. 1991;48:173-182.##Wobus AM, Boheler KR, Embryonic Stem Cells: prospects for developmental biology and cell therapy. Physiol Rev. 2005;85:635-78.##Winkler J, Hescheler J, Sachinidis A. Embryonic stem cells for basic research and potential clinical applica-tions in cardiology. Biochim Biophys Acta. 2005;1740 (2):240-8.##Sachinidis AK, Fleischmann B, Kolossov E. Cardiac specific differentiation of mouse embryonic stem cells.  Cardio Rese. 2003;58:278-291.##Kumar D, Sun B. TGF-beta 2 enhances differentia-tion of cardiac myocytes from embryonic stem cells. Biochem Biophys Res Commun. 2005;332:135-41.##Maltsev VA, Rohwedel J, Hescheler J. Embryonic stem cells differentiate in vitro into cardiomyocytes representing sinusnodal, atrial and ventricular cell types. Mech Dev. 1993;44:41-50.##Czyz J, Wobus AM. Embryonic stem cell differentia-tion: the role of extracellular factors. Differentiation. 2001;8:167-74.##Schuldiner M, Yanuka O. Effects of eight growth factors on the differentiation of cells derived from human embryonic stem cells. Proc Natl Acad Sci USA. 2000;97:11307-11312.##Behfar A, Zingman LV, Hodgson DM. Stem cell differentiation requires a paracrine pathway in the heart. FASEB J. 2002;16:1558-66.##Orkin SH. GATA-binding transcription factors in hematopoietic cells.  Blood. 1992;80:575-581.##Simon MC. Gotta have GATA. Nat Genet. 1995;11:9-11.##Zhu J, Hill RJ, Heid PJ. End-1 encodes an apparent GATA factor that specifies the endoderm precursor in Caenorhabditis elegans embryos. Genes Dev. 1997;11: 2883-96.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>بررسي اثر فاكتور رشد NGF، RA، Shh بر تمايز سلول‌هاي بنيادي جنيني موش به سلول‌هاي عصبي و اليگوسيتي</TitleF>
    <TitleE>Evaluating the effects of NGF, RA and Shh growth factors on murine embryonic stem cell differentiation into neurons and oligocytes</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: سلول‌هاي بنيادي جنيني (ES) سلول‌هاي همه تواني هستند كه توانايي تمايز به انواع سلول‌هاي تخصصي بالغ را دارا مي‌باشند و در حال حاضر و آينده نزديك امكان استفاده از اين سلولها در درمان بسياري از بيماريها با روش سلول درماني وجود دارد. به نظر مي‌رسد در آينده بتوان برخي بيماري‌هاي سيستم عصبي را با استفاده از فاكتورهاي مؤثر بر تمايز سلول‌هاي بنيادي به سلول‌هاي عصبي و گليالي درمان نمود، لذا در اين تحقيق سلول‌هاي بنيادي جنيني موش به صورت همه توان و تمايز نيافته كشت و تكثير داده شد و سپس تأثيرات فاكتورهاي رشد NGF، Shh، RA به منظور القاي تمايز اين سلولها به سلول‌هاي عصبي و گليالي مورد بررسي قرار گرفت.
روش بررسي: سلول‌هاي بنيادي جنيني (از موش نژاد 129 بنام CCB) را روي فيبروبلاست جنيني موش نژاد C57/BL6 كشت و تكثير داده و با روش قطرات معلق از آنها اجسام جنيني (EBs) تهيه شد. بعد از انتقال و كشت كلوني‌هاي EBs بر روي پليت كشت پوشانيده با فيبرونكتين، فاكتورهاي القایی NGF وShh به ترتيب با غلظت‌هاي ng/ml50 و 100، ng/ml300 و 500 و RA با غلظت  M1و در گروه‌هاي ديگر bFGF با غلظت ng/ml20 به محيط كشت اختصاصي سلول‌هاي پيش‌ساز عصبي اضافه شد تا سلولها به سمت تمايز عصبي هدايت شوند. به منظور بررسي تمايز به انواع سلول‌هاي عصبي و گليالي با روش RT-PCR بيان ژن‌هاي اختصاصي سلول‌هاي عصبي شامل S100، Olig-2،Nurr-1، Nkx2.2 و Nestin ارزيابي شد و علاوه بر اين از روش ايمونوسيتوشيمي براي تأييد حضور پروتئين MAP-2 استفاده شد.
نتايج: در اين تحقيق، بررسي‌هاي مولكولي نشان داد كه هر يك از اين فاكتورهاي رشد با تأثير در بيان ژن‌هاي‌ اختصاصي سلول‌هاي عصبي يك يا چند مسير مولكولي را فعال مي‌كنند كه در تمايز سلول‌هاي مختلف سيستم عصبي نقش اساسي دارند. رنگ‌آميزي اختصاصي اين سلولها با آنتي‌بادي MAP-2 نشان داد كه سلول‌هاي حاصل داراي زوائد دندريتي خاص سلول‌هاي عصبي يا نورون هستند. 
نتيجه‌گيري: براساس يافته‌هاي اين تحقيق سلول‌هاي بنيادي جنيني همه توان و تمايز نيافته در حضور  فاكتورهاي رشد RA، NGF، Shh به سلول‌هاي عصبي و اوليگودندروسيتي تمايز مي‌يابند؛ به‌طوريكه هر يك از اين عوامل در مسير خاص تمايزي سلول‌هاي تخصصي سيستم عصبي مؤثر بوده و حتي ميزان غلظت افزوده شده عوامل فوق نيز بر چگونگي تمايز يافتن اين سلولها مؤثر مي‌باشد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Embryonic stem (ES) cells are pluripotent cells that can differentiate into all types of specific adult cells and are used for cell therapy in certain diseases. It seems that the inductive factors may be used to produce neurons and gliocytes out of ES cells for the treatment of some nervous system diseases in future. In this research, pluripotent and undifferentiated murine embryonic cells were cultured and effects of the growth factors NGF, RA and Shh were studied for the induction of neural and glial differentiations.
Materials &amp; Methods: CCB ES cell line derived from  mouse strain 129 were cultured on inactivated embryonic fibroblasts from C57/BL6 mice and embryonic bodies (EBs) were pre-pared and transplanted onto culture plates covered by fibronectin and growth factors NGF, Shh and RA with respective concentrations of  50 and 100 ng/ml, 300 and 500 ng/ml and 1 μM and  in some groups bFGF with a concentration of 20 ng/ml were added to the specific culture medium for neural cell precursors to induce cell differentiation into neural cells. For studying differentiation into many types of neurons and oligodendrocyte, gene expression of specific neu-ral genes such as nestin, Nkx2-2, Nurr1, S100 and Olig-2 were assessed by RT-PCR and immu-nocytochemistry assays were used to confirm the presence of MAP-2 protein.
Results: In this study, genetic evaluations showed that each of the previously mentioned growth factors activate some molecular mechanisms that have essential effects on differentiation into different kinds of nervous system cells by affecting the expression of marker genes. Cytoche-mistry of these cells by monoclonal MAP-2 antibody showed the resultant cells have dendrites that are specific for neural cells or neurons.
Conclusion: The findings indicated that pluripotent and undifferentiated CCB ES cells underwent differentiation into neural cells and oligodendrocytes under the effects of NGF, Shh and RA growth factors and this neural induction was confirmed by the presence of molecular and antigenic markers in these cells. Each of these factors was effective in the induction of different-tiation of specialized neural cells and even different concentrations of the factors induced parti-cular cell differentiations.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>349</FPAGE>
            <TPAGE>358</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Hediyeh</Name>
<MidName>H</MidName>
<Family>Jahanbakht</Family>
<NameE>هدیه</NameE>
<MidNameE></MidNameE>
<FamilyE>جهان‌بخت</FamilyE>
<Organizations>
<Organization>Department of Biology, Faculty of Sciences, Islamic Azad University, Science &amp;amp; Research Campus</Organization>
</Organizations>
<Universities>
<University>Department of Biology, Faculty of Sciences, Islamic Azad University, Science &amp; Research Campus</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Kazem</Name>
<MidName>K</MidName>
<Family>Parivar</Family>
<NameE>کاظم </NameE>
<MidNameE></MidNameE>
<FamilyE>پریور</FamilyE>
<Organizations>
<Organization>Department of Biology, Faculty of Sciences, Islamic Azad University, Science &amp;amp; Research Campus</Organization>
</Organizations>
<Universities>
<University>Department of Biology, Faculty of Sciences, Islamic Azad University, Science &amp; Research Campus</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Mehdi</Name>
<MidName>MM</MidName>
<Family>Akhondi</Family>
<NameE>محمدمهدی</NameE>
<MidNameE></MidNameE>
<FamilyE>آخوندی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>akhondi@avicenna.ac.ir</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mahmood</Name>
<MidName>M</MidName>
<Family>Jeddi-Tehrani</Family>
<NameE>محمود </NameE>
<MidNameE></MidNameE>
<FamilyE>جدی‌تهرانی</FamilyE>
<Organizations>
<Organization>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</Organization>
</Organizations>
<Universities>
<University>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Hossein</Name>
<MidName>MH</MidName>
<Family>Modarresi</Family>
<NameE>محمدحسین </NameE>
<MidNameE></MidNameE>
<FamilyE>مدرسی </FamilyE>
<Organizations>
<Organization>Nanobiotechnology Research Center, Avicenna Research Institute (ACECR)</Organization>
</Organizations>
<Universities>
<University>Nanobiotechnology Research Center, Avicenna Research Institute (ACECR)</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Reza</Name>
<MidName>MR</MidName>
<Family>Sadeghi</Family>
<NameE> محمدرضا</NameE>
<MidNameE></MidNameE>
<FamilyE>صادقی</FamilyE>
<Organizations>
<Organization>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</Organization>
</Organizations>
<Universities>
<University>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad</Name>
<MidName>M</MidName>
<Family>Keramatipour</Family>
<NameE>محمد</NameE>
<MidNameE></MidNameE>
<FamilyE>کرامتی پور</FamilyE>
<Organizations>
<Organization>Faculty of Medical Tehran University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Faculty of Medical Tehran University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Amir Hassan</Name>
<MidName>AH</MidName>
<Family>Zarnani</Family>
<NameE>امیرحسن</NameE>
<MidNameE></MidNameE>
<FamilyE>زرنانی</FamilyE>
<Organizations>
<Organization>Nanobiotechnology Research Center, Avicenna Research Institute (ACECR)</Organization>
</Organizations>
<Universities>
<University>Nanobiotechnology Research Center, Avicenna Research Institute (ACECR)</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Sheida</Name>
<MidName>Sh</MidName>
<Family>Salehkhou</Family>
<NameE>شیدا</NameE>
<MidNameE></MidNameE>
<FamilyE>صالح‌خو</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Murine</KeyText></KEYWORD><KEYWORD><KeyText>Embryonic stem cell</KeyText></KEYWORD><KEYWORD><KeyText>Differentiation</KeyText></KEYWORD><KEYWORD><KeyText>Neuron</KeyText></KEYWORD><KEYWORD><KeyText>RA</KeyText></KEYWORD><KEYWORD><KeyText>NGF</KeyText></KEYWORD><KEYWORD><KeyText>Shh</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>256.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Gardner RL, Cockroft DL. Complete dissipation of coherent clonal growth occurs before gastrulation in mouse epiblast. Development. 1998;125(13):2397-402.##Martin GR. Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells. Proc Natl Acad Sci USA. 1981;78(12):7634-8.##Brook FA, Gardner RL. The origin and efficient deriva-tion of embryonic stem cells in the mouse. Proc Natl Acad Sci USA. 1997;94(11):5709-12.##Evans MJ, Kaufman MH. Establishment in culture of pluripotential cells from mouse embryos. Nature. 1981; 9;292(5819):154-6.##Wichterle H, Lieberam I, Porter JA, Jessell TM. Direct-ed differentiation of embryonic stem cells into motor neurons. Cell. 2002;110(3):385-97.##Weissman IL, Anderson DJ, Gage F. Stem and proge-nitor cells: origins, phenotypes, lineage commitments, and transdifferentiations. Annu Rev Cell Dev Biol. 2001;17:387-403.##Bain G, Kitchens D, Yao M, Huettner JE, Gottlieb DI Embryonic stem cells express neuronal properties in vitro. Dev Biol. 1995;168(2):342-57.##Briscoe J, Pierani A, Jessell TM, Ericson J. A homeo-domain protein code specifies progenitor cell identity and neuronal fate in the ventral neural tube. Cell. 2000; 101(4):435-45.##Yung SY, Gokhan S, Jurcsak J, Molero AE, Abrajano JJ, Mehler MF. Differential modulation of BMP signal-ing promotes the elaboration of cerebral cortical GABAergic neurons or oligodendrocytes from a com-mon sonic hedgehog-responsive ventral forebrain progenitor species. Proc Natl Acad Sci U S A. 2002; 10;99(25):16273-8.##Gilbert Scott F. Developmental biology, sinuar U 6th  Edition. 2000;pp:272-409.##Novitch BG, Chen AL, Jessell TM. Coordinate regu-lation of motor neuron subtype identity and pan-neuro-nal properties by the bHLH repressor Olig2. Neuron. 2001;31(5):773-89.##Burbach JP, Smits S, Smidt MP. Transcription factors in the development of midbrain dopamine neurons. Ann N Y Acad Sci. 2003;991:61-8. Review.##Marshak DR, Gardner RL, Gottlieb D. Stem Cell Biology. CSHL press. 2000;pp:250-1.##Martinat C, Bacci JJ, Leete T, Kim J, Vanti WB, Newman AH, Cha JH, Gether U, Wang H, Abeliovich A. Cooperative transcription activation by Nurr1 and Pitx3 induces embryonic stem cell maturation to the midbrain dopamine neuron phenotype. Proc Natl Acad Sci USA. 2006;103(8):2874-9.##Chang L, Jones Y, Ellisman MH, Goldstein LS, Karin M. JNK1 is required for maintenance of neuronal mic-rotubules and controls phosphorylation of microtubule-associated proteins. Dev Cell. 2003;4(4):521-33.##بربرستانی محمد، نوروآناتومی پایه وپزشکی، نشر نور دانش (1379)، صفحات: 29-20.##Almazan G, Honegger P, Du Pasquier P, Matthieu JM Dexamethasone stimulates the biochemical differentia-tion of fetal forebrain cells in reaggregating cultures. Dev Neuro Sci. 1986;8(1):14-23.##Bain G, Kitchens D, Yao M, Huettner JE, Gottlieb DI Embryonic stem cells express neuronal properties in vitro. Dev Biol. 1995;168(2):342-57.##Fraichard A, Chassande O, Bilbaut G, Dehay C, Sava-tier P, Samarut J. In vitro differentiation of embryonic stem cells into glial cells and functional neurons. J Cell Sci. 1995;108(Pt 10):3181-8.##Okabe S, Forsberg-Nilsson K, Spiro AC, Segal M, McKay RD. Development of neuronal precursor cells and functional postmitotic neurons from embryonic stem cells in vitro. Mech Dev. 1996;59(1):89-102.##Mujtaba T, Piper DR, Kalyani A, Groves AK, Lucero MT, Rao MS. Lineage-restricted neural precursors can be isolated from both the mouse neural tube and cultured ES cells. Dev Biol. 1999;214(1):113-27.##Li M, Pevny L, Lovell-Badge R, Smith A. Generation of purified neural precursors from embryonic stem cells by lineage selection. Curr Biol. 1998;(8):971-974.##Rolletschek A, Chang H, Guan K, Czyz J, Meyer M, Wobus AM. Differentiation of embryonic stem cell-derived dopaminergic neurons is enhanced by survival-promoting factors. Mech Dev. 2001;105(1-2):93-104.##Garner CC, Tucker RP, Matus A. Selective localiza-tion of messenger RNA for cytoskeletal protein MAP2 in dendrites. Nature. 1988;336(6200):674-7.##Binder LI, Frankfurter A, Rebhun LI. Differential localization of MAP-2 and tau in mammalian neurons in situ. Ann N Y Acad Sci. 1986;466:145-66.##Yung SY, Gokhan S, Jurcsak J, Molero AE, Abrajano JJ, Mehler MF. Differential modulation of BMP signa-ling promotes the elaboration of cerebral cortical GABAergic neurons or oligodendrocytes from a common sonic hedgehog-responsive ventral forebrain progenitor species. Proc Natl Acad Sci USA. 2002;99 (25):16273-8.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>بررسی تأثیر داروی آتورواستاتین بر کشت بافت اندومتر انسان در زمینه سه بعدی فیبرینی</TitleF>
    <TitleE>Evaluating the effects of Atorvastatin on cultured human endometrium in a three-dimensional fibrin matrix</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمینه و هدف: آندومتريوز به عنوان يكي از عوامل اصلي ناباروري در زنان تحقيقات گسترده‌اي را به خود اختصاص داده است. کشت بافت اندومتر انسانی در زمینه سه بعدی فیبرینی به عنوان مدل مناسبی برای بیماری اندومتریوز مطرح مي‌باشد. استاتینها به‌عنوان داروهايي با اثرات متنوع در رگ‌زايي به عنوان كانديداي براي مهار اين بيماري مطرح مي‌باشند. لذا هدف مطالعه حاضر، شناسائي تأثیر غلظت‌های مختلف آتورواستاتین بر کشت بافت اندومتر انسانی به منظور تعیین اثرات مهار یا تسريع‌کننده آن بر رشد بافت مي‌باشد.
روش بررسی: 8 نمونه بافت اندومتر طبيعي انسان به قطعات mm11 تقسیم و در ظروف 24 خانه، کشت داده شدند. براي تشكيل مدل سه بعدي مورد نظر ابتدا به هر خانه از ظرف كشت ml5/0 محلول فیبرینوژن در محيط M199 با غلظت mg/ml 3 و L 10 ترومبین اضافه گردید. پس از تشكيل ژل، قطعات بافت اندومتر در سطح آن قرار داده‌شد و لایه دوم از محلول فیبرینوژن اضافه گردید. قطعات بافت اندومتر هر نمونه در 4 ردیف 5 تایی چاهك‌هاي ظرف کشت داده شدند. ردیف اول به عنوان کنترل محيط كشت و ردیف‌هاي دوم تا چهارم به ترتيب غلظت‌هاي m1/0، m1 و m10 از آتورواستاتين به چاهكها اضافه گرديد. هر 72 ساعت تعویض محیط انجام شد و تغییرات ایجاد شده در بافتها با استفاده از میکروسکوپ معكوس ثبت گردید. همچنین در روز‌های 1، 7، 14 و 21 از نمونه‌ها عکسبرداری صورت گرفت. در پایان دوره مطالعه، به بافت‌های کشت داده شده براساس مشاهدۀ رشد زوائد سلولی، هجوم سلول های رسوب یافته به درون ژل فیبرین و رشد غدد آندومتری نمره داده شد و تصاویر مربوط به کشت سه بعدی آنالیز شد. همچنین به منظور تائید ساختار های سلولی رشد یافته در ژل، برش های پارافینی به  دست آمده از نمونه های کشت داده شده به روش ایمونوهیستوشیمی و با آنتی ویمنتین، آنتی سیتوکراتین و آنتی CD31 رنگ آمیزی شدند. براي آنالیز آماری داده‌ها از نرم‌افزار آماری SPSS (نسخه 5/11) استفاده شد. داده‌های مربوط به نمره دهی بافتها توسط آزمون آماری فريدمن و داده‌های حاصل از آنالیز تصاویر توسط آزمون آماریANOVA  یکطرفه مورد تجزیه و تحلیل قرار گرفت.
نتایج: تغييرات رشد در گروه کنترل، 5/82% و در گروه M1/0، 5/87% بود كه اختلاف آنها معنی‌دار بود (05/0p&lt;). اين تغييرات در گروه M1، 50% و در گروه M10، 5% بود که اختلاف آنها نيز با گروه کنترل معنی‌دار بود (001/0p&lt;). 
نتیجه‌گیری: داروی آتورواستاتین در غلظت‌هاي مختلف داراي اثرات متفاوتي بر رشد بافت اندومتر کشت داده شده مي‌باشد به ‌طوري كه با دوز M1/0 باعث افزایش رشد و دوزهای M1 و M10 باعث کاهش رشد می‌گردد. مطالعات تکمیلی در مدل‌های حیوانی در این زمینه توصیه می‌شود.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Endometriosis, as one of the main causes of infertility in women, has devoted a lot of research to itself. Three-dimensional culture of human endometrial tissue has been known as a functional model for endometriosis. Statins have a variety of different effects on angiogenesis and they have been suggested as a candidate for the inhibition of this disease. Therefore, the aim of the present study is to determine inhibitory or promotory effects of different concentrations of Atorvastatin on the growth of cultured human endometrium.
Materials &amp; Methods: 8 endometrial samples were cut into 1x1 mm pieces and were cultured in 24-well culture plates. To establish the desired three-dimensional model, 0.5 ml of fibrinogen solution in M199 medium, with a concentration of 3mg/ml and 10&#181;L of thrombin were added to each well. After formation of the jelly, the endometrial fragments were placed on it and a second jelly layer was added. The endometrial tissue of each specimen was cultured in four 5-piece layers. The first row was regarded as control and to the second, third and forth rows, 0.1, 1.0 and 10&#181;M concentrations of the medication were added respectively. Every 3 days, endometrial pieces and their probable changes were observed by an invert microscope (Motic-AE31) and the culture media were changed. The tissue fragments were also photographed on days 1, 7, 14 and 21. At the end of the study, the cultures were graded according to their cellular outgrowths, invasion of deposited cells into the jelly and growth of endometrial glands and images related to the 3-D cultures were analyzed. To confirm the growth of cellular structures into the jelly, paraffin embedded cuts of the cultured specimen were immunohistochemically stained by anti-vimentin, anticytokeratin and anti-CD31. The data were analyzed by SPSS statistical software (Version 11.5). The statistical analysis related to the grading of wells was done by Freedman test and the statistical analysis of the images was performed by one-way ANOVA.
Results: Growth changes were 82.5% in the control group and 87.5% in the 0.1&#181;M concentration group, depicting significantly higher values compared to the control group (p&lt;0.05). The changes in 1&#181;M and in 10&#181;M  groups were 50% and  5%  respectively which had  significant differences with that of the control group (p&lt;0.001).
Conclusion: Different concentrations of Atorvastatin have different effects on the growth of cultured endometrial tissue, 0.1&#181;M concentration increases growth of cultured human endomet-rium, while 1&#181;M and 10&#181;M can decrease growth of the tissue. Further animal studies on this subject are suggested.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>358</FPAGE>
            <TPAGE>367</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Azadeh</Name>
<MidName>A</MidName>
<Family>Montaseri</Family>
<NameE>آزاده</NameE>
<MidNameE></MidNameE>
<FamilyE>منتصری</FamilyE>
<Organizations>
<Organization>Reproduction Research Center, Kermanshah University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Reproduction Research Center, Kermanshah University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>montaseri_azi@yahoo.com</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mozaffar</Name>
<MidName>M</MidName>
<Family>Khazaei</Family>
<NameE> مظفر</NameE>
<MidNameE></MidNameE>
<FamilyE>خزاعی</FamilyE>
<Organizations>
<Organization>Reproduction Research Center, Kermanshah University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Reproduction Research Center, Kermanshah University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Rostam</Name>
<MidName>R</MidName>
<Family>Ghorbani</Family>
<NameE>رستم</NameE>
<MidNameE></MidNameE>
<FamilyE>قربانی</FamilyE>
<Organizations>
<Organization>Reproduction Research Center, Kermanshah University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Reproduction Research Center, Kermanshah University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mansour</Name>
<MidName>M</MidName>
<Family>Rezaei</Family>
<NameE>منصور</NameE>
<MidNameE></MidNameE>
<FamilyE>رضایی</FamilyE>
<Organizations>
<Organization>Reproduction Research Center, Kermanshah University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Reproduction Research Center, Kermanshah University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Atorvastatin</KeyText></KEYWORD><KEYWORD><KeyText>Endometrium</KeyText></KEYWORD><KEYWORD><KeyText>Endometriosis</KeyText></KEYWORD><KEYWORD><KeyText>3D-culture</KeyText></KEYWORD><KEYWORD><KeyText>Tissue growth</KeyText></KEYWORD><KEYWORD><KeyText>Fibrin</KeyText></KEYWORD><KEYWORD><KeyText>Thrombin</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>257.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Lebovic DI, Bentzien F, Chao VA, Garrett ET, Taylor RN. Induction of an angiogenic phenotype in endomet-riotic stromal cell culture by interlukine-1 beta. Mol Hum Reprod. 2000;6:269-75.##Strathy JH, Mdgaard CA, Coulam CB, Melton LJ.  Endometriosis and infertility: A laparoscopic study of endometriosis among fertile and infertile women. Fertil  Steril. 1982;38:667-72.##Kettle LM, Hummel WP. Modern medical management of endometriosis. Obset Gynecol Clin North Am. 1997; 24:361-73.##Adamson GD, Nelson HP. Surgical treatment of endo-metriosis. Obset Gynecol Clin North Am. 1997;24: 375-409.##Sampson JA. Peritoneal endometriosis due to menstrual dissemination of endometrial tissue into peritoneal cavity. Am J Obset Gynecol. 1927;14:422-9.##Healy DL, Rogers PAW, Hill L, Wingfield M. Angio-genesis: a new theory for endometriosis. Hum Reprod Update. 1998;4(5):736-40.##Fasciani A, Bocci G, Xu J, Bielecki R, Greenblatt E, Leyland N, Casper R C. Three-dimensional in vitro culture of endometrial explants mimics the early stage of endometriosis. Fertil Steril. 2003;80(5):1137-43.##Khazaei M, Esfandiari N, Javed M, Gotlieb L, Casper RC. Successful of human secretory phase endometrium culture as an In vitro model for endometriosis. Fertil  Steril. 2004;82(2):S164.##Khazaei M, Esfandiari N, Gotlieb L, Casper RC. Angiogenesis following three-dimensional culture of isolated human endometrial stroma cells. Fertil  Steril. 2004; 82 (2): S61.##Lea AP, Mc Tavish D. Atorvastatin. A review of its pharmacology and therapeutic potential in the manage-ment of hyperlipidemias. Drugs. 1997;35(5):828-47.##Graaf MR. The risk of cancer in users of statins. J Clin Oncol. 2004;22(12):2388-94.##Ruiz-Velasco. Statins upregulate CD 36 expressin in human monocytes an affect strengthened when com-bined with PPAR-gamma ligand putative contribution of Rho GTPase in statin-induced CD36 expression. Biochem Pharmacol. 2004;67(2):303-13.##Laufs U. Beyond lipid-lowering: effects of statins on endothelial nitric oxide. Eur J Clin Pharmacol. 2003; 58(11): L719-31.##Esfandiari N, Khazaei M, Ai j, Bielecki R, Gotlieb L, Ryan E, Casper R. Effect of statin on an in vitro model of endometriosis. Fertil  Steril. 2006;87(2):257-62.##Wierzbicki AS. Atorvastatin. Expert Opin Pharmaco-ther. 2001;2(5):819-30.##Malinowski JM.: Atorvastatin: a hydroxylmethylgl-utaryl-coenzyme A reductase inhibitpor. Am J Health Syst Pharm. 1998;55(21):2253-67.##Vincent L, Chen W, Hong L. Inhibition of endothelial cell migration by cerivastatin, an HMG-CoA reductase inhibitor: contribution to its anti-angiogenic effect. FEBS Lett. 2001;495:159-66.##Kureishi Y, Luo Z, Shiojima I. The HMG-CoA reduc-tase inhibitor simvastatin activates the protein kinase akt and promotes angiogenesis in normocholeste-rolemic animals. Nat Med. 2000;6:1004-10.##Weis M, Heeschen C, Glassford A, Cooke J. Statins have Biphasic effects on angiogenesis. Circulation. 2002;105:739-46.##Rorowski A, Walsh K. Statin therapy and angiogene-sis. Curr Opin Lipidol. 2003;14(6):599-603.##Walter DH, Zeiher AM, Dimmeler S. Effects of statins on endothelium and their contribution to neovasculariza-tion by mobilization of endothelial progenitor cells. Coron Artery Dis. 2004;15(5):235-242.##Littman BA, Smotrich DB, Stillman RJ. Endometrio-sis; Principal and practice of endocrinology and metabolism, 2nd Edn. Philadelphia JB. Lippincott Com-pany. 1995;906-9.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>اثر گياه آب بشقابي بر روند اسپرماتوژنز رت</TitleF>
    <TitleE>Evaluating the effects of Centella asiatica on spermatogenesis in rats</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: با توجه به حمايت‌هاي سازمان بهداشت جهاني از حفظ سلامت جامعه و كنترل جمعيت و نيز بهداشت باروري، امروزه استفاده از فرآورده‌هاي گياهي به عنوان جانشين يا مكمل داروهاي سنتزي ضد بارداري مطرح مي‌باشد. گياه آب بشقابي (Centella Asiatica) گونة با ارزشي است كه در طب سنتي از هزاران سال پيش در كشورهاي آسياي شرقي، هندوستان و چين به طور سنتي براي درمان بيماري‌هاي مختلف استفاده شده است. اين گياه در ايران در منطقه تالاب بندرانزلي به صورت وحشي پراكنش دارد و تحقيقاتي در رابطه با تأثير آن بر سيستم توليد مثلي در مدل آزمايشگاهي انجام نشده است؛ لذا بر اين اساس هدف از اين مطالعه، بررسي اثرات عصاره تام گياه آب بشقابي بر روي عملكرد اسپرماتوژنز در رت‌هاي نر بود. 
روش بررسي: ابتدا گياه از تالاب بندرانزلي جمع‌آوري و به روش پركولاسيون، عصاره تام آن تهيه شد. سپس موش‌هاي صحرايي نر نژاد ويستار 10-8 هفته و با وزن g250-200 به صورت تصادفي انتخاب و به گروه‌هاي شش‌تايي تقسيم شدند. آنگاه دوزهاي mg/kg 100 و80، 50،10 از عصاره، انتخاب و روزانه به مدت 60 روز به صورت خوراكي به رتها داده شد. پس از آخرين دوز دريافتي رت‌هاي مورد آزمايش، گروه كنترل و شم تشريح شدند. سپس بيضه‌هاي آنها به دقت جدا شده و به منظور بررسي اثرات احتمالي عصاره بر وزن اندام‌هاي توليد مثلي طي مدت درمان در گروه‌هاي مورد مطالعه، كنترل و شم بيضه‌ها وزن شدند. سپس آناليز پارامترهاي اسپرم و بررسي‌هاي بافت‌شناسي بيضه انجام گرفت. نتايج حاصل با استفاده از نرم افزارهاي آماري Pharm, SPSS و آزمون واريانس يك طرفه با سطح معني‌داري 05/0p&lt; تجزيه و تحليل آماري شد.
نتايج: نتايج نشان داد كه مقدار LD50 براي عصاره تام گياه در رت‌هاي نر mg500 با حدود اطمينان 2/2-9/1 مي‌باشد. بر اين اساس دوزهاي غيركشنده mg/kg 100، 80، 50، 10 جهت ارزيابي عملكرد اسپرم و بررسي‌هاي بافت‌شناسي بيضه در نظر گرفته شد. نتايج تغييرات وزن بدن و بيضه در حيوانات دريافت كننده غلظت‌هاي مختلف عصاره در مقايسه با گروه كنترل و شم افزايش معني‌داري را نشان داد. همچنين بررسي‌هاي بافت‌شناسي، تغييراتي در سير تكامل اسپرماتوژنز، شامل از بين رفتن اسپرماتوزوئيدها، پرخوني بافت بينابيني در برخي توبول‌هاي اسپرم‌ساز و نتايج آناليز اسپرم كاهش معني‌داري در ميزان اسپرم‌هاي زنده (01/0p&lt;) و متحرك (001/0p&lt;) و ذخيره اسپرم در اپيديديم (001/0p&lt;) نسبت به گروه كنترل و شم نشان داد؛ ولي تغيير در مورفولوژي اسپرم مشاهده نشد. 
نتيجه‌گيري: با توجه به نتايج حاصل، به نظر مي‌رسد بتوان از اين گياه به عنوان عامل ضد باروري موقت در حيوانات استفاده كرد. نويسندگان مقاله تحقيقات بيشتري را در زمينه بيوشيميايي و مولكولي اثر اين عصاره بر روي سيستم توليد مثلي توصيه مي‌كنند تا مسائلي همچون به صرفه بودن اقتصادي و فرمولاسيون مناسب مورد بررسي قرار گيرد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Based on supportive aids of WHO in the field of public health, family planning and reproductive health, consumption of herbal drugs has been considered as an alternative to synthetic contraceptive drugs. Centella asiatica has been traditionally used for the treatment of different types of diseases for thousands of years in various parts of the world including Eastern Asia, China and India. Considering the dispersal of this plant in Bandar Anzali’s wetlands and lack of research on the effects of this plant on reproductive system in laboratory models, this study was carried out to evaluate the effects of Centella asiatica extract on spermatogenesis and testical tissue of rats.
Materials &amp; Methods: At first, the plant was collected and its extract was prepared through percolation process. Some 8 to 10-week old male Wistar rats, weighing about 200-250 grams, were selected randomly and were divided into 6-member subgroups. The rats in the control group received water, the sham group received Tween solvent and the third to the sixth groups received non-fatal doses of 10, 50, 80 and 100mg/kg of the crude extract for 60 days respectively. On the 61st day, the rats were dissected and their testes were taken out and weighed for probable effects of the extract on the organs weight. Then sperm parameters and histological evaluations of the testes were done. The results were analyzed by the use of SPSS and Pharm softwares by calculation of one-way ANOVA while considering p&lt;0.05 as the significance level. 
Results: The LD50 of the plant was calculated as 500mg/kg, with a confidence interval of 1.9- 2.2 in male rats. The non-lethal doses of 10, 50, 80 and 100 mg/kg of Centella extract were considered for histological and spermatogonial evaluations. There were significant increases in body and testis weight in rats receiving the extract compared to the control and sham groups. There were histological changes during spermatogonial evolution such as degeneration of spermatozoa and interstitial congestion in some tubules and sperm analysis showed a meaningful decrease in the number of spermatozoa (p&lt;0.01), motile sperms (p&lt;0.001) and epididymal sperm storage (p&lt;0.001) compared to the sham and control groups but there were no changes in sperm morphology.     
Conclusion: Based on the above results, it seems that Centella asiatica can be used as a temporary contraceptive agent in animals. Nevertheless, more biochemical and molecular research on the contraceptive effects of this extract is needed to determine its economical benefits and prepare an appropriate formulation.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>367</FPAGE>
            <TPAGE>375</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Mahnaz</Name>
<MidName>M</MidName>
<Family>Heidari</Family>
<NameE>مهناز</NameE>
<MidNameE></MidNameE>
<FamilyE>حیدری</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>mheidari@avicenna.ac.ir</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Amir Hasan</Name>
<MidName>AH</MidName>
<Family>Jamshedi</Family>
<NameE>امیرحسن</NameE>
<MidNameE></MidNameE>
<FamilyE>جمشیدی</FamilyE>
<Organizations>
<Organization>Ministry of Health &amp;amp; Medical Education</Organization>
</Organizations>
<Universities>
<University>Ministry of Health &amp; Medical Education</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Shahin</Name>
<MidName>Sh</MidName>
<Family>Akhondzadeh</Family>
<NameE>شاهین</NameE>
<MidNameE></MidNameE>
<FamilyE>آخوندزاده</FamilyE>
<Organizations>
<Organization>Faculty of Medical Tehran University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Faculty of Medical Tehran University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Maerefat</Name>
<MidName>M</MidName>
<Family>Ghaffari</Family>
<NameE>معرفت</NameE>
<MidNameE></MidNameE>
<FamilyE>غفاری نوین</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Reza</Name>
<MidName>MR</MidName>
<Family>Sadeghi</Family>
<NameE> محمدرضا</NameE>
<MidNameE></MidNameE>
<FamilyE>صادقی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mahmoud</Name>
<MidName>M</MidName>
<Family>Ghazi Khansari</Family>
<NameE>محمود</NameE>
<MidNameE></MidNameE>
<FamilyE>قاضی خوانساری</FamilyE>
<Organizations>
<Organization>Faculty of Medical Tehran University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Faculty of Medical Tehran University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Mehdi</Name>
<MidName>MM</MidName>
<Family>Akhondi</Family>
<NameE>محمدمهدی</NameE>
<MidNameE></MidNameE>
<FamilyE>آخوندی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Rat</KeyText></KEYWORD><KEYWORD><KeyText>Sperm</KeyText></KEYWORD><KEYWORD><KeyText>Spermatogenesis</KeyText></KEYWORD><KEYWORD><KeyText>LD50</KeyText></KEYWORD><KEYWORD><KeyText>Centella asiatica</KeyText></KEYWORD><KEYWORD><KeyText>Fertility</KeyText></KEYWORD><KEYWORD><KeyText>Contraceptives</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>258.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Rechinger KH. Flora Iranica. (Umbelliferae). Akade-mische Druck-U. Verlagsanstalt. Graz-Austria. 1987; vol:162;39.##Mozaffarian V. The family of umbelliferae in iran (keys and distribution). Research Institute of Forests and Rangelands. Iran. 1983;23-24.##World Health Organization. Monographs on Selected Medicinal Plants. WHO. Geneve. 1998;77-85.##Schultz V, Hansel R, Tyler V. Rational phytotherapy: a physicians guid to herbal medicine.4th Edition, Springer. Germany. 2000;pp:337-338.##Corpoter DO. Nursing herbal medicine handbook. Sprinhouse. Pennsylvania. 2001;pp:213-214.##Carpenter D. Professional guide to complementery and alternative therapies. Springhouse, Pensylvania. 2002; pp:239-240.##Sastravaha G, Yotnuengnit P, BoonCong P, Sangthera-pitikul P. Adjunctive periodontal treatment with cen-tella asiatica and punica granatum extracts, A prelimi-nary study. J Int Acad Periodontal. 2003;5(4): 106-12.##Kuhn MA. Herbal theraphy and supplements. Lippin-cott, New york. 2000;pp:163-66.##کمیته تدوین فارماکوپه گیاهی ایران‌ـ فارماکوبه گیاهی ایران، وزارت بهداشت درمان و آموزش پزشکی، سال 84، صفحات 99-107.##Dutta T, Basu UP. Crude extract of Centella asiatica and products derived from its glycosides as oral anti-fertility agents. Indian J Exp Biol. 1968;6(3):181-2.##Gruenwald J, Brendle Jaenicke C. PDR for herbal medicine. 2nd Edition. Medical Economics Co. Mont-vale New Jersey. 2000;729-31.##Jalili A, Jamzad Z. Red data book of plant species of iran. Research institute of forests and rangelands. Iran. 1999;pp:663.##Murray MT. The healing power of herbs Rocklin. California, Prima Publishing. 1995;pp:173-83.##Garg S, Doncel G, Chabra S, Upadhyay SN, Talwar GP. Synergistic spermicidal activity of neem seed extract, reetha saponins and quinine hydrochloride. Contraception. 1994;50:185-90.##Sander FV, Cramer SD. A practicall method of testing the spermicidal action of chemical contraceptives.Hum Fertil. 1998;6:134.##Seed J, Chapin RD, Clegg ED. Methods for assessing sperm motility, morphology, and counts in the rat, rabbit, and dog consensus repot. ILSI Risk science Institute Expert working group on sperm evalution. Report Toxicol. 1996;10:237-244.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>مقايسه تيتر آنتی‌بادی IgG کلاميديا پنومونيه در مبتلايان به پره‌اکلامپسی با شروع زودرس و ديررس </TitleF>
    <TitleE>Comparing serum IgG titers against Chlamydia pneumoniae in patients with early and late-onset pre-eclampsia and healthy individuals</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: پره‌اکلامپسی همچنان يکی از معضلات عمده سلامت مادران و نوزادان می‌باشد. چندين وجه مشترک بين پره‌اکلامپسی و آترواسکلروز وجود دارد. قبلاً ارتباط بين ابتلاء به عفونت مزمن کلاميديا پنومونيه و ايجاد آترواسکلروز نشان داده شده است. اين مطالعه با هدف تعيين وجود ارتباط بين پاتوژنز و زمان وقوع پره‌اکلامپسی و عفونت مزمن با کلاميديا پنومونيه انجام شده است.
روش بررسی: اين مطالعه مقطعی روی 88 زن با نتيجه طبيعی بارداري، 72 زن مبتلا به پره‌اکلامپسی ديررس و 16 زن مبتلا به پره‌اکلامپسی زودرس طي سال‌های 83 و 84 در شهر زاهدان انجام شد. در کليه افراد وضعيت سرم افراد برای وجود IgG عليه کلاميديا پنومونيه و تيتر آن با روش الايزا تعيين شد. سپس اطلاعات مربوط به مشخصات دموگرافيک و وضعيت آنتی‌بادی در نرم افزار SPSS وارد و با استفاده از آمار توصيفی، آزمون‌های آناليز واريانس يک طرفه و مجذور کای مورد تجزيه و تحليل قرار گرفت. مقدار 05/0&gt;p از نظر آماری معنی‌دار درنظر گرفته شد.
نتايج: نتايج نشان داد که بين سه گروه از نظر وجود آنتي‌بادي عليه كلاميديا پنومونيه تفاوتی وجود نداشت. به عبارت ديگر بين هر دو گروه از مبتلايان به پره‌اکلامپسی زودرس و ديررس، مبتلايان به پره‌اکلامپسی زودرس و گروه شاهد و مبتلايان به پره‌اکلامپسی ديررس و گروه شاهد از نظر سروپازتيويتي تفاوت معني‌داري نداشت. اما معلوم شد که از نظر تيتر آنتی‌بادی IgG عليه کلاميديا پنومونيه بين سه گروه (0001/0&gt;p) و بين هر دو گروه مبتلايان به پره‌اکلامپسی زودرس و ديررس  و مبتلايان به پره‌اکلامپسی زودرس و گروه شاهد (0001/0&gt;p) تفاوت معنی‌داری وجود داشت؛ ولی بين گروه مبتلايان به پره‌اکلامپسی ديررس وگروه شاهد تفاوتی موجود نبود. 
نتيجه‌گيری: نتايج اين مطالعه نشان داد که عفونت مزمن با كلاميديا پنومونيه می‌تواند با پره‌اکلامپسی زودرس در ارتباط باشد. اين بررسی می‌تواند پشتوانه‌ای جهت يافتن ارتباط پره‌اکلامپسی و آترواسکلروز بعدی باشد. لذا پيشنهاد مي‌شود احتمال استفاده از ماكروليدها به عنوان جزئي از برنامه‌هاي پيشگيري در افراد در معرض خطر ابتلا به پره‌اكلامپسي مورد بررسي قرار گيرد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Pre-eclampsia is one of the complexities of maternal and neonatal health. There are several similarities between pre-eclampsia and atherosclerosis. The relation between chronic Chla-mydia pneumoniae infections with atherosclerosis has been shown previously. This study has been done to determine the connection between pathogenesis and onset time of pre-eclampsia and chro-nic Chlamydia pneumoniae infection.
Materials &amp; Methods: This cross-sectional study was done on 88 women with normal pregnancy outcomes, 72 patients with late-onset pre-eclampsia and 16 patients who developed early-onset pre-eclampsia in Zahedan in the years 2004-2005. Anti-Chlamydia IgG and its titer were checked for in the cases and controls by ELISA method. After entering the demographic data and IgG status of  the study population, statistical analysis was performed using SPSS software by one-way ANOVA and Chi-Square test, at a significance level of p&lt;0.05.
Results: The results showed that there were no difference in seropositivity among the three groups (p=0.4). There were also no differences between early-onset and late-onset pre-eclampsia (p=0.5), early-onset pre-eclampsia and control group (p=0.32) and late-onset pre-eclampsia and control group (p=0.25) in that regard. There was a significant difference in IgG titers among the three groups (p&lt;0.0001), between early-onset and late-onset pre-eclampsia (p&lt;0.0001) and between early-onset pre-eclampsia and control group (p&lt;0.0001), but there were no differences between those with late-onset pre-eclampsia and the control group (p=0.98).
Conclusion: The results of this study showed that chronic infection with Chlamydia pneumoniae could be related to early-onset pre-eclampsia. This study can be a support for evaluating the relationship between pre-eclampsia and subsequent atherosclerosis. Therefore, it is suggested that use of macrolides be part of the preventive programs in high-risk individuals for pre-eclampsia.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>375</FPAGE>
            <TPAGE>383</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Mojgan</Name>
<MidName>M</MidName>
<Family>Mokhtari</Family>
<NameE>مژگان</NameE>
<MidNameE></MidNameE>
<FamilyE>مختاری</FamilyE>
<Organizations>
<Organization>Department of Obs. &amp;amp; Gyn., Ali-Ebne-Abitaleb Hospital, Faculty of Medicine, Zahedan University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Department of Obs. &amp; Gyn., Ali-Ebne-Abitaleb Hospital, Faculty of Medicine, Zahedan University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>mmokhtari1345@hotmail.com</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Minoo</Name>
<MidName>M</MidName>
<Family>Yaghmaei</Family>
<NameE>مینو</NameE>
<MidNameE></MidNameE>
<FamilyE>یغمایی</FamilyE>
<Organizations>
<Organization>Department of Obs. &amp;amp; Gyn., Ali-Ebne-Abitaleb Hospital, Faculty of Medicine, Zahedan University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Department of Obs. &amp; Gyn., Ali-Ebne-Abitaleb Hospital, Faculty of Medicine, Zahedan University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mehrbod</Name>
<MidName>M</MidName>
<Family>Karimi</Family>
<NameE>مهربد</NameE>
<MidNameE></MidNameE>
<FamilyE>کریمی</FamilyE>
<Organizations>
<Organization>Department of Pathology, Ali-Ebne-Abitaleb Hospital, Faculty of Medicine, Zahedan University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Department of Pathology, Ali-Ebne-Abitaleb Hospital, Faculty of Medicine, Zahedan University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Masoud</Name>
<MidName>M</MidName>
<Family>Roodbari</Family>
<NameE>مسعود</NameE>
<MidNameE></MidNameE>
<FamilyE>رودباری</FamilyE>
<Organizations>
<Organization>Department of Epidemiology &amp;amp; Statistics , Faculty of Health, Zahedan Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Department of Epidemiology &amp; Statistics , Faculty of Health, Zahedan Medical Sciences University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Hamid Reza</Name>
<MidName>HR</MidName>
<Family>Koohpaye</Family>
<NameE>حمیدرضا</NameE>
<MidNameE></MidNameE>
<FamilyE>کوهپایه</FamilyE>
<Organizations>
<Organization>Department of Infectious Diseases, Bu-Ali Hospital, Faculty of Medicine, Zahedan University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Department of Infectious Diseases, Bu-Ali Hospital, Faculty of Medicine, Zahedan University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Pregnancy outcome</KeyText></KEYWORD><KEYWORD><KeyText>Preeclampsia</KeyText></KEYWORD><KEYWORD><KeyText>Chlamydia infections</KeyText></KEYWORD><KEYWORD><KeyText>Chlamydia pneumoniae</KeyText></KEYWORD><KEYWORD><KeyText>Antibodies</KeyText></KEYWORD><KEYWORD><KeyText>ELISA</KeyText></KEYWORD><KEYWORD><KeyText>Atherosclerosis</KeyText></KEYWORD><KEYWORD><KeyText>Macrolides</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>259.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Roberts JM. Preeclampsia: what we know and what we do not know. Semin Perinatol. 2000;24(1):24-8.##Campbell DM. Mac Gillivray I. Preeclampsia in twin pregnancies: Incidence and outcome .Hypertens Preg-nancy. 1999;18:197-203.##Von Dadelszen P, Magee LA. Could an infectious trig-ger explain the differential maternal response to the shared placental pathology of preeclampsia a normo-tensive intrauterine growth restriction?. Acta Obstet Gynecol Scand. 2002;81(7):642-8.##Sibai BM. Hypertension. In: Gabbe SG, Niebyl JR, Si-mpson JL. Obstetrics Normal and problem pregnan-cies. 4th Edition, Published by Churchill Livingstone, New York. 2002;pp:945-89.##Roberts JM. Pregnancy-Related Hypertension In: Crea-sy RK, Resnik R. Maternal-Fetal Medicine. 4th Edition, Published by W.B. Saunders Company, Philadelphia. 1999:843.##Roberts JM, Taylor RN, Musci TJ, Rodgers GM, Hubel CA, MeLaughlin MK. Preeclampsia: an endothelial cell disorder. Am J Obstet Gynecol. 1989;161:1200-4.##Von Dadelszen P, Magee LA, Marshall JR, Rotstein OD. The maternal syndrome of preeclampsia: a former fruste of the systemic inflammatory response syndrome Sepsis. 2000;4:43-7.##Roberts JM. Endothelial dysfunction in preeclampsia. Semin Reprod Endocrinol. 1998;16(1):5-15.##Raynor BD, Bonney EA, Jang KT, Coto W, Garcia MS. Preeclampsia and Chlamydia pneumoniae: is there a link? Hypertens Pregnancy. 2004;23(2):129-34.##Smith GC, Pell JP, Walsh D. Pregnancy complications and maternal risk of ischemic heart disease: a retros-pective cohort study of 129,290 births. Lancet. 2001; 357(9273):2002-6.##Hertig AT. Vascular pathology in the hypertensive albuminuric toxemias of pregnancy. Clinics. 1945;4 (602):614.##Von Dadelszen P, Magee LA, Krajden M, Alasaly K, Popovska V, Devarakonda RM, Money DM, Patrick DM, Brunham RC. Levels of antibodies against cyto-megalovirus and chlamydophila pneumoniae are increased in early onset preeclampsia. BJOG. 2003; 110:725-30.##Anderson TJ. Assessment and treatment of endothelial dysfunction in humans. J Am Coll Cardiol. 1999;34: 631-8.##Liao JK, Endothelium and acute coronary syndromes. Clin Chem. 1998;44:1799-808.##Silva Neto LB, Ribeiro JP. Infectious agents in coro-nary athero sclerosis. Arq. Bras Cardiol. 1999;73(5): 455-62.##Criqui MH. Epidemiology of cardiovascular disease. In: Goldman L, Ausiello D. Cecil Text Book of Medi-cine. 22nd Edition, Published by Saunders, Philadel-phia. 2004;pp:253.##Morre SA, Stooker W, Lagrand WK, Van den Brule AJC, Niessen HWM. Microorganisms in the etiology of atherosclerosis. J Clin Pathol. 2000;53:647-54.##Heine RP, Ness RB, Roberts JM. Seroprevalence of antibodies to Chlamydia pneumoniae in women with preeclampsia. Obstet Gynecol. 2003;102(1):198-9.##Goulis DG, Chappell L, Gibbs RG, Williams D, Dave JR, Taylor P. Association of raised titers of antibodies to Chlamydia pneumoniae with a history of pre-eclampsia. BJOG. 2005;112(3):299-305.##Report of the National High Blood Pressure Education Program Working Group on High Blood Pressure in Pregnancy. Am J Obstet Gynecol. 2000;183(1):S1-S22.##Cunningham FG, Leveno KJ, Bloom SL, Hauth JC, Gilstrap lll LC, Wenstrom KD. Williams Obstetrics. 22nd Edition, Published by McGraw-Hill, New York. 2005;pp:762-83.##Vallance P, Collier J, Bhagat K. Infection, infla-mmation and infarction: does acute endothelial dys-function provide a link?. Lancet. 1997;349:1391-2.##Stille W, Dittmann R. Arteriosclerosis as a sequela of chronic Chlamydia pneumoniae infection. Herz. 1998; 23:185-92.##Maass M. Persistence of Chlamydia pneumoniae in human arteriosclerotic plaque substance. Evidence and consequences. Herz. 1998;23:187-4.##Goldman L. Cardiovascular Diseases. In: Drazen JM, Gill GN, Griggs RC, Kokko JP, Mandell GL, Powell DW, et al. Cecil Text book of Medicine, 21st Edition, Published by Sannders Company, Philadelphia. 2000: 295.##Anderson TJ. Assessment and treatment of endothelial dysfunction in humans. J Am Coll Cardiol. 1999:34; 631-8.##Liao JK. Endothelium and acute coronary syndromes. Clin Chem. 1998;44:1799-808.##Benitez RM. Atherosclerosis: an infection disease?. Hosp Prac. 1999;34(9):79-90.##Xu Q. Infections, heat shock proteins, and athero-sclerosis. Curr Opin Cardiol. 2003;18(4):245-52.##Boggess KA, Lieff S, Murtha AP, Beck J, Offen-bacher S. Periodontal disease and hypertensive compli-cations of pregnancy [abstract]. Hypertens Pregnancy. 2000;19(supp 1):16.##Faas MM, Schuiling GA, Linton EA, Sargent IL, Redman CW. Activation of peripheral leukocytes in rat pregnancy and experimental preeclampsia. Am J Obstet Gynecol. 2000;182(2):351-357.##Mittendorf R, Lain KY, Williams MA, Walker CK. Preeclampsia. A nested, case-control study of risk factors and their interactions. J Reprod Med. 1996;41 (7):491-6.##Agastsuma Y, Fitzpatrick P, Lele A, Kaul A, Ogra PL. Cell-mediated immunity to cytomegalovirus in preg-nant women. Am J Reprod Immunol. 1981;1(4);174-9.##Von Dadelszen P, Magee LA, Lee SK. Activated protein C in normal human pregnancy and pregnancies complicated by severe preeclampsia: a therapeutic opportunity?. Crit Care Med. 2002;30:1883-92.##Von Dadelszen P, Wilkins T, Redman CWG. Mater-nal peripheral blood leukocytes in normal and preec-lamptic pregnancies. Br J Obstet Gynaecol. 1999;106: 576-81.##Chaouat G, Tranchot DJ, Volumenic JL. Immune suppression and Th1/Th2 balance in pregnancy revisi-ted. Am J Reprod Immunol. 1997;37(6):427-34.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>نقش لاپاروسکوپی در درمان مردان آزواسپرم با بیضه‌های غیرقابل لمس</TitleF>
    <TitleE>The role of laparoscopy in the management of azoospermic men with Non-palpable testis</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: يكي از تظاهرات باليني مردان با بيضه‌هاي غيرقابل لمس، ناباروري و آزواسپرمي است. تشخيص و درمان بيضه‌هاي غيرقابل لمس به خصوص در نزد بالغين بحث برانگيز مي‌باشد. روش‌های تصویربرداری معمول نظیر سونوگرافی، CTS Scan و MRI جهت یافتن بیضه‌های غیرقابل لمس از حساسیت کافی برخوردار نبوده و جواب‌هاي منفی کاذب بالایی دارند. بدین ترتیب در این بیماران لاپاروسکوپی ضروری می‌باشد. اگرچه مطالعاتی در خصوص فواید لاپاروسکوپی در این بیماران صورت گرفته است؛ ولی هنوز موارد بحث برانگیز زیادی وجود دارد که ضرورت چنین مطالعاتی را نشان می‌دهد. اين مطالعه به بررسي نقش لاپاروسكوپي در تشخيص و درمان (غالباً اركيكتومي) مردان نابارور با آزواسپرمي ناشي از بيضه‌هاي غيرقابل لمس مي‌پردازد.
روش بررسي: بررسي حاضر از نوع Case series بود و پرونده و فيلم لاپاروسكوپي بيماران مراجعه كننده به مركز فوق ‌تخصصي درمان ناباروري ابن‌سينا از بهمن 83 تا آبان 85 مورد بررسي قرار گرفت. در طي مدت مطالعه 12 بيمار متأهل با 20 بيضه غيرقابل لمس با ناباروري اوليه و آزواسپرم، داراي اندیکاسیون لاپاروسكوپي ارزيابي شدند. پس از ارزيابي اوليه رضايت‌نامه مربوط به انجام اركيكتومي احتمالي از بيماران دريافت شد. بعد از آمادگي‌هاي لازم قبل عمل جراحي، براي اين افراد لاپاروسكوپي تشخيصي‌ـ درماني انجام شد. در موارديكه عروق اسپرماتيك به صورت كور و انتهایشان قابل رؤيت بود به لاپاروسكوپي خاتمه داده شد. سپس با توجه به اندازة بيضه، فاصله تا رينگ داخلي و سن بيمار تصميم به اركيوپکسی و يا اركيكتومي گرفته شد.
نتایج: 20 بیضه غیرقابل لمس در نزد 12 بیمار کریپتورکیديسم یک يا دو طرفه تحت بررسی قرار گرفت. متوسط سنی این بیماران به هنگام مراجعه و انجام عمل لاپاروسکوپی 37 سال (43-33) بود. در معاینه بالینی 8 بیمار بیضه غیرقابل لمس دو طرفه و 4 بیمار یک بیضه قابل لمس آتروفيك داشتند که 2 مورد با نزول طبیعی و 2 مورد هم ارکیوپکسی با جراحی باز در سن بعد بلوغ بود. از 20 بیضه غیرقابل لمس که تحت عمل لاپاراسکوپی قرار گرفتند 5 بیضه (25%) وجود نداشت که 3 مورد بيضه محو شده بود که عناصر طناب منوي به صورت انتهای کور نرسیده به رينگ داخلي قابل رویت بودند و 2 بیضه (10%) هم اركيكتومي به روش جراحی باز شده بودند. 15 بیضه دیگر (60%) داخل شکمی بودند که به‌طور موفقیت‌آمیزی تحت عمل ارکیوپکسی یا ارکیکتومی لاپاروسکوپی قرارگرفتند. عارضه‌ای در ارتباط با لاپاروسکوپی دیده نشد. نمونه‌های اركيكتومي و نیز بیوپسی بیضه‌های اركيوپكسي شده به پاتولوژی ارسال گرديد که از 15 نمونه پاتولوژی، براي 3 بيمار آتروفي بیضه، براي 3 بیمار بیضه نابالغ و براي 9 بيمار آپلازي سلول‌های ژرمینال گزارش گردید.
نتیجه‌گیری: لاپاروسکوپی یک روش مؤثر و بدون خطر در درمان بیضه‌های غیرقابل لمس در بالغین است. بیماران از درد کمتر، نقاهت کوتاه، ظاهر عالی و ترخیص سریع سود می‌برند. اين مطالعه استفاده روتین از روش لاپاروسکوپی را در تشخیص و درمان بیضه‌های غیرقابل لمس بالغین پيشنهاد مي‌كند.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Infertility and azoospermia are among the clinical presentations of males with im-palpable testis. The management of non-palpable testis especially in adult patients remains contro-versial. Routine imaging methods like sonography, CTS and MRI are not sensitive enough to detect impalpable testes and have high false negative results. Therefore, it is necessary to perform laparoscopic examination in such patients. Although a few studies have reported benefits of lapa-roscopic examinations in the management of such cases, but it is still subject to many contro-versies showing the need for more investigations in this area. The aim of this study is to evaluate the role of laparoscopy in the diagnosis and treatment (mostly orchiectomy) of impalpable testis in azoospermic men.
Materials &amp; Methods: This is a case series study in which the files and laparoscopy movies of patients who had attended Avesina Infertility Clinic form February 2006 to October 2005 and had indication for laparoscopy were retrospectively analyzed. During the study twenty testicular units from 12 married patients with primary infertility and azoospermia were studied. After preliminary evaluations, informed consent for probable orchiectomy was taken from the patients. After preo-perative preparations, diagnostic/surgical laparoscopies were performed. In cases of blind ending vessels or vanishing testes, the procedure was terminated. Orchiopexy or orchiectomy was per-formed based on testis size, distance from internal ring and patient’s age.
Results: Twenty testicular units from 12 patients with unilateral or bilateral cryptorchidism were studied. The mean age of patients at the time of attendance and laparoscopy was 37 years (33-43). Eight patients presented bilateral non-palpable testes and four patients with palpable one-sided atrophic testis, two patients had natural descents and two had undergone postpubertal orchiopexy. From the 20 impalpable testes undergoing the procedure, 5 (25%) were absent, 3 vanishing testes and 2 previously done orchiectomies. 15 out of the 20 testes (60%) were located in intra-abdo-minal cavity and were managed successfully by the means of laparoscopic orchiopexy or orchiec-tomy. No laparoscopy related complications occurred. All testicular biopsies from orchiopexy or orchiectomy were sent to a pathology laboratory. Three of the 15 biopsies were reported as atro-phic testis, three as immature testis and 8 of them had germ cell aplasia. 
Conclusion: The data suggest that laparoscopy can be considered as a safe and effective method for the management of non-palpable testis in adults. The patients may experience less pain and benefit from better cosmetics, early discharge and rapid recovery.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>383</FPAGE>
            <TPAGE>391</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Naser</Name>
<MidName>N</MidName>
<Family>Amirjannati</Family>
<NameE>ناصر</NameE>
<MidNameE></MidNameE>
<FamilyE>امیرجنتی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>namirjannati@yahoo.com</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Mehdi</Name>
<MidName>MM</MidName>
<Family>Akhondi</Family>
<NameE>محمدمهدی</NameE>
<MidNameE></MidNameE>
<FamilyE>آخوندی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Hooman</Name>
<MidName>H</MidName>
<Family>Sadri-Ardekani</Family>
<NameE>هومن </NameE>
<MidNameE></MidNameE>
<FamilyE>صدری‌اردکانی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Haleh</Name>
<MidName>H</MidName>
<Family>Soltanghoraee</Family>
<NameE> هاله</NameE>
<MidNameE></MidNameE>
<FamilyE>سلطان قرایی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mahmood</Name>
<MidName>M</MidName>
<Family>Jeddi-Tehrani</Family>
<NameE>محمود </NameE>
<MidNameE></MidNameE>
<FamilyE>جدی‌تهرانی</FamilyE>
<Organizations>
<Organization>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</Organization>
</Organizations>
<Universities>
<University>Monoclonal Antibody Research Center, Avicenna Research Institute (ACECR)</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Hossein</Name>
<MidName>MH</MidName>
<Family>Modarresi</Family>
<NameE>محمدحسین </NameE>
<MidNameE></MidNameE>
<FamilyE>مدرسی </FamilyE>
<Organizations>
<Organization>Nanobiotechnology Research Center, Avicenna Research Institute (ACECR)</Organization>
</Organizations>
<Universities>
<University>Nanobiotechnology Research Center, Avicenna Research Institute (ACECR)</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Impalpable testis</KeyText></KEYWORD><KEYWORD><KeyText>Azoospermia</KeyText></KEYWORD><KEYWORD><KeyText>Orchiopexy</KeyText></KEYWORD><KEYWORD><KeyText>Laparoscopic orchiectomy</KeyText></KEYWORD><KEYWORD><KeyText>Andrology surgery</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>260.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
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    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>بررسی آگاهی، نگرش و رفتارهای زنان در مورد بهداشت باروري در هفت شهر مرکزی ایران، 1384</TitleF>
    <TitleE>Evaluating knowledge, attitude and behavior of women on reproductive health subjects in seven central cities of Iran</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمینه و هدف: گسترش بهداشت باروری و پرداختن به ابعاد مختلف آن در سطح ملی و بین‌المللی یکی از گام‌های اساسی در تامین سلامت جامعه و خانواده با محور سلامت زنان می‌باشد. با توجه به اینکه در تعریف جدید، بهداشت باروری به تمامی جنبه‌های زندگی و سلامت زنان و دختران وابسته است و هم اکنون بهداشت باروری و بهره‌مند شدن زنان از حقوق باروری خود به عنوان بخشی از حقوق اساسی بشر و حمایت‌های مذهبی دین اسلام از آن مطرح است، این تحقیق با هدف تعیین آگاهی، نگرش و رفتارهای زنان در زمینه بهداشت باروری انجام گرفت.
روش بررسی: این بررسی مطالعه‌ای توصیفی‌ـ تحلیلی از نوع مقطعی می‌باشد که در هفت شهر مرکزی ایران در سال 1384 انجام شد. نمونه‌های مورد بررسي، 840 نفر از زنان 49-15 ساله مراجعه کننده به مراکز بهداشتی درمانی بودند كه به روش نمونه‌گیری سه مرحله‌ای وارد تحقیق شدند. ابزار گردآوری اطلاعات پرسشنامه بود که به روش مصاحبه تکمیل و در نرم افزار آماری SPSS ويرايش 5/11 وارد و تجزیه و تحلیل گردید. آزمون‌هاي آماری مورد استفاده در اين تحقيق، آزمون ناپارامتري كروسكال‌ـ واليس، 2 و آزمون همبستگي پيرسون بود.  
نتایج: طبق نتایج 62% زنان با اصطلاح بهداشت باروری آشنایی داشتند و4/66% آنان روش‌هاي مؤثر پيشگيري از بارداري را به كار مي‌بردند؛ هرچند زنان مورد بررسی از حداکثر نمره آگاهی (14) میانگین نمره 21/9 را کسب کردند؛ در عین حال فقط حدود 18% آنان از زمان مناسب انجام آزمایش پاپ اسمیر و خودآزمایی پستان آگاهی داشتند و سوءتعابیری نیز در مورد ایدز در بین آنان وجود داشت. آزمون ناپارامتری کروسکال والیس اختلاف معنی‌داری بین آگاهی زنان در شهرهاي مورد مطالعه و مقاطع تحصیلی مختلف نشان داد (05/0p&lt;). نگرش زنان در خصوص بهداشت باروری مطلوب بود ولی در شهرهای مختلف تفاوت معنی‌داری داشت (05/0p&lt;). 
نتیجه‌گیری: با توجه به نتایج فوق و اهمیت مقوله بهداشت و حقوق باروری و تأکید دین اسلام بر روی این موضوع ارتقاء آگاهی، نگرش و رفتارهای زنان در زمینه بهداشت باروری مقوله‌هایی مانند آزمایش پاپ اسمیر، خودآزمایی پستان و استفاده از روش‌های مطمئن پیشگیری از بارداری باید در دستور کار سیاستگزاران بهداشتی و سازمان‌های غیردولتی در شهرهاي مورد مطالعه قرار گیرد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Reproductive health and paying attention to its different dimensions in national and international levels are the essential steps in providing social and family health, with an emphasis on women&#39;s health. Regarding the new applications of the term, “Reproductive Health” is dependent upon all aspects of girls&#39; and women&#39;s lives and health. The point that women should enjoy their reproductive health, reproductive rights are considered as parts of human rights and also considering Islam’s support for this issue, the present research was carried out to determine women’s knowledge, attitude and behavior on reproductive health subjects.
Materials &amp; Methods: This is a cross-sectional and analytical-descriptive study carried out in seven central cities of Iran in 2005. The subjects consisted of 840 married women, aged 15-49 years, who attended urban and rural health centers and were selected in a 3-stage sampling method. The instrument for data collection was a questionnaire completed through interviews. The data were entered into and analyzed by SPSS, version 11.5. Applied statistical tests in this research was Kruskal- Wallis non parametric test, 2 and Pearson correlation test.
Results: According to the results, 62% of the women were familiar with the term reproductive health and 66.4% of them used effective contraceptive methods, although they obtained an average of 9.21 (from a maximum mark of 14 for knowledge), just 18% of them knew the appropriate time for Pap smear and breast self-exam and also there were many misconceptions on HIV/AIDS. Kruskal-Wallis test showed a significant difference between awareness of women in various cities with their educational achievements (p&lt;0.05). Women&#39;s attitude about reproductive health was good but there were significant differences among women from different cities (p&lt;0.05). The women’s behavior in many categories, such as Pap smear, breast self-exam and use of safe contraception methods need to be enhanced.
Conclusion: Regarding the results and importance of women&#39;s reproductive health and rights, as well as instructive advocacy of Islam on the matter, promoting women&#39;s knowledge, attitude and behavior on reproductive health must be included on the agenda of health policy makers and non-governmental organizations in studied cities.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>391</FPAGE>
            <TPAGE>401</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Seyyed Saeed</Name>
<MidName>SS</MidName>
<Family>Mazloomy Mahmood-Abad</Family>
<NameE>سید سعید</NameE>
<MidNameE></MidNameE>
<FamilyE>مظلومی محمود آباد</FamilyE>
<Organizations>
<Organization>School of Public Health, Shahid Sadoughi University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>School of Public Health, Shahid Sadoughi University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>mazloomy_s@yahoo.com</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Fatemeh</Name>
<MidName>F</MidName>
<Family>Shahidi</Family>
<NameE>فاطمه</NameE>
<MidNameE></MidNameE>
<FamilyE>شهیدی</FamilyE>
<Organizations>
<Organization>Healthy Behavior &amp;amp; Health Promotion Research Center, Shahid Sadoughi University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Healthy Behavior &amp; Health Promotion Research Center, Shahid Sadoughi University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Masoumeh</Name>
<MidName>M</MidName>
<Family>Abbasi-Shavazi</Family>
<NameE>معصومه</NameE>
<MidNameE></MidNameE>
<FamilyE>عباسی شوازی</FamilyE>
<Organizations>
<Organization>Healthy Behavior &amp;amp; Health Promotion Research Center, Shahid Sadoughi University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Healthy Behavior &amp; Health Promotion Research Center, Shahid Sadoughi University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Fatemeh</Name>
<MidName>F</MidName>
<Family>Shahrizadeh</Family>
<NameE>فاطمه</NameE>
<MidNameE></MidNameE>
<FamilyE>شهری‌زاده</FamilyE>
<Organizations>
<Organization>Healthy Behavior &amp;amp; Health Promotion Research Center, Shahid Sadoughi University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Healthy Behavior &amp; Health Promotion Research Center, Shahid Sadoughi University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Women</KeyText></KEYWORD><KEYWORD><KeyText>Reproductive health</KeyText></KEYWORD><KEYWORD><KeyText>Reproductive rights</KeyText></KEYWORD><KEYWORD><KeyText>Family planning</KeyText></KEYWORD><KEYWORD><KeyText>Contraceptive method</KeyText></KEYWORD><KEYWORD><KeyText>Knowledge</KeyText></KEYWORD><KEYWORD><KeyText>Attitude</KeyText></KEYWORD><KEYWORD><KeyText>Behavior</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>261.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Ministry of Health and Medical Education Burea of Population and Family Health. ‎Population and health in the Islamic Republic of Iran: Demographic and  Health Servey(DHS). 1st ed. Tehran: unicef; 2000.p 52-78. persian.##Zanjani H, Shadpour K, Mirzaei M, Mahryar AH. Population development. 6th ed.Tehran: Boshra; 2003. p 116-7.##Hatami H, Razavi SM, Eftekhar H, Majlesi F,Seyed Nozadi M, Parizadeh MJ. Textbook of public health. 3rd ed. Tehran: Arjmand; 2004. p 1354-72.##Roudi-Fahimi. Womens Reproductive Health In The Middle East And North AFRICA, MENA Policy Brief, Population Reference Bureau. pp:1-8.##Jaffer YA, Afifi M, Al Ajmi F, Alouhaishi K. Know-ledge, attitudes and practices of secondary-school pupils in Oman: II. Reproductive health. East Mediterr Health J. 2006;12(1-2):50-60.##Leeman L. Medical barriers to effective contraception. Obstet Gynecol Clin North Am. 2007;34(1):19-29.##John Everett P. ‎Textbook of preventive and social medicine, a treatise on community health. 3rd ed. Shjaei Tehrani H, translator. Gilan: Gilan University of Medical Science. 1996. p 121-3.##Chichakli LO, Atrash HK, Musani AS, Johnson JT, Mahaini R, Arnaoute S. Family Planning  Services  and  programmes in Countries of The Eastern Mediterrane-an  Region. East Mediterr Health J. 2000;6(4):614-24.##Ministry of Health and Medical Education Burea of Population and Family Health. Population and family planning in the Islamic Republic of Iran. Tehran: Ministry of Health and Medical Education; 2004. p110.##Abou Shabana K, el-Shiek M, el-Nazer M, Samir N. Womens perceptions and practices regarding their  rights to reproductive health. East Mediterr Health J. 2003;9(3):296-308.##Graham A, Dawson W, Moore L. Emergency  contra-ception. Health Educ J. 2000;59:329-339.##Hardon Antia A, Kabir S, Engelkes E. Monitoring  Family  Planning  and  Reproductive  Rights. Published by Zed books, London. 1997:pp:18.##پاک سرشت صدیقه، عودی مونا. سرطان پستان و غربالگری، فصلنامه پژوهشی دانشکده‌های پرستاری و مامایی استان گیلان: سال 16 (بهار و تابستان1383)، صفحات: 6-5.##King MT, Kenny P, Shiell A, Hall J, Boyages J. Quality of Life three month and one year after first treatment for early  Stage breast  Cancer: influence of treatment and patient characteristics. Qual Life Res. 2000;9(7):789-800.##وظیفه شناس‌آذر، مبرهن یکتایی ملک النساء، سرطان سرویکس. فصلنامه پژوهشی دانشکده‌های پرستاری و مامایی استان گیلان: سال16 (بهار و تابستان 1383)، صفحات: 26-24.##شفیعی فروغ، عباسی شوازی معصومه، عباسی شوازی محمد تقی، عبادی فردآذر فربد، ارزشیابی تأثیر آموزش واحد درسی جمعیت و تنظیم خانواده بر آگاهی و نگرش دانشجویان دانشکده مهندسی برق دانشگاه یزد، سال 1383. مجله ایرانی آموزش در علوم پزشکی: 1384، شماره 14، ویژه نامه خلاصه مقالات هفتمین همایش کشوری آموزش پزشکی، آبان 384، صفحات 63-62.##شجاعی‌زاده داوود، موسوی سید محمد حسین. مدل‌های مطالعه رفتارهای در آموزش بهداشت. چاپ اول، اتشارات وزارت بهداشت، درمان و آموزش پزشکی (1379)، صفحات: 21 و 25.##Strecher VJ, Rosenstock IM. The health belief model. In Glanz k, Lewis FM, Rimer BK (Editors). Health Behavior and Health Education theory, Research and practice.2nd Edition. San Francisco: Jossey-Bass. 1997; pp:41-59.##Quek JT, Li Sc. A study of the effectiveness of AIDS Health education Interventions among the adolescent population of Singapore. Singapore Med J. 2002; 43 (7):359-64.##Cunnigham F, Mcdonald P, Levenok K. Cesarean  Section and  Cesarean  hysterectomy. Williams obstet-rics. 19 th texa. Prentice Hail International. INC. 1993; 591-4.##توسلی مریم، حیدرنیا محمدعلی، غفرانی‌پور فضل ا...، رمضانزاده فاطمه، بررسی تأثیر آموزش در کاهش سزارین انتخابی در خانم‌های باردار. فصلنامه پژوهشی طلوع بهداشت: خلاصه مقالات اولین کنگره سراسری آموزش بهداشت، سال 2 (تابستان و پائیز 1382)، شماره 2 و 3، صفحه 39.##عباسی شوازی محمد جلال، حسینی چاووشی میمنت، دلاور بهرام، حاملگی ناخواسته و عوامل مؤثر بر آن در ایران. فصلنامه باروری و ناباروری: سال پنجم (1382)، شماره 1، صفحات: 76-62.##شجاعی زاده داوود، چالشگر مشرفه، پاشایی طاهره، تعیین میزان شیوع حاملگی ناخواسته و عوامل مؤثر بر آن در زنان باردار 49-15 ساله در شهرستان قائم شهر در سال 1383. فصلنامه پژوهشی طلوع بهداشت: سال 3 (زمستان 1383)، شماره 4، صفحات: 26-20.##حلم سرشت پریوش، دل پیشه اسماعیل. جمعیت و تنظیم خانواده. انتشارات چهر ( 1379)، صفحات: 105 و 113.##شکیبا مهرداد، طباطبایی افسر، کریمی مهران، بررسی حاملگی ناخواسته در استان یزد در سال 80- 1379. فصلنامه پژوهشی طلوع بهداشت: سال 1 (زمستان 1381)، شماره 2، صفحات: 30-26.##بلبل حقیقی ناهید، ابراهیمی حسین، عجمی محمد اسماعیل، مقایسه فراوانی زایمان طبیعی و سزارین و علل آن در شهرستان شاهرود در سال 1379. فصلنامه پژوهشی باروری و ناباروری: سال3(بهار 1381)، شماره 10،  صفحات: 58-51.##مرکز بهداشت استان یزد، واحد تنظیم خانواده، آمار سالیانه پوشش پاپ اسمیر در استان یزد در سالهای 1381، 1382، 1383.##باقیانی مقدم محمد حسین، احرام پوش محمد حسن، میرزایی منصور، فاضل پور شکوه، منابع مورد استفاده زنان 49-15 ساله استان یزد در زمینه آگاهیهای کسب شده نسبت به بهداشت مادر و کودک و تنظیم خانواده، فصلنامه پژوهشی طلوع بهداشت: سال 3 (بهار 1383)، شماره 1، صفحات: 45-39.##سیام  شهره، بررسی نحوه عملکرد زنان شهر رشت درباره تنظیم خانواده. فصلنامه پژوهشی طلوع بهداشت: خلاصه مقالات اولین کنگره سراسری آموزش بهداشت، سال 2(تابستان و پائیز 1382)، شماره 2 و 3،  صفحه 39.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>تشخیص و درمان لوکوسیتواسپرمی در مردان نابارور</TitleF>
    <TitleE>Identification and treatment of leukocytospermia in infertile men</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>نقش لوكوسيتها در دستگاه تناسلي مردان و مايع مني پيچيده و ديناميك است. لوكوسيتها در هر انزال وجود دارند و در سطوح مختلف فعاليت مي‌كنند. وجود تعداد زياد لوكوسيتها در مايع مني، نشانه مهمي دال بر وجود عفونت يا التهاب دستگاه تناسلي مرد است. از سوی دیگر در بسياري از مطالعات لوكوسيتواسپرمي با ناباروري مرد همراهي داشته است. كاهش تعداد، میزان حركت اسپرمها و همچنين افزايش درصد شكل‌هاي غيرطبيعي آنها و افزايش سلول‌هاي ژرمينال نابالغ در مردان مبتلا به لوكوسيتواسپرمي گزارش شده است. سازمان بهداشت جهاني، وجود یک میلیون WBC يا بيشتر در هر ميلي‌ليتر مايع مني را معادل لوكوسيتواسپرمي تعريف مي‌كند. مشكلات تكنيكي در افتراق سلول‌هاي ژرمينال نابالغ موجود در مايع مني از لكوسيتها وجود دارد. براي اهداف باليني، عملي‌ترين روش براي تشخيص لوكوسيت در مايع مني، رنگ‌آميزي پراكسيداز است.
مطالعات مختلف نشانگر محدوده وسيعي از شيوع لوکوسیتواسپرمی 2% تا حد 35% در بيماران نابارور است. عمده بررسيها در گروه‌هاي جمعيتي با تعداد زیاد بيماران، شيوعي در حد 20-12% را در تمام بيماران نابارور نشان مي‌دهد.
تصور اينكه لوكوسيتواسپرمي فقط نتيجه عفونت دستگاه تناسلي مرد است، اشتباه است. عوامل محيطي همچون استعمال دخانيات، مصرف الكل و همچنين ماري‌جوانا تعداد لكوسيتها را در مايع مني افزايش مي‌دهد. پرهيز طولاني مدت از مقاربت و برخي روش‌هاي ارتباط جنسي (مثل مقاربت مقعدي) مي‌تواند موجب لوكوسيتواسپرمي شود. امروزه مستندات علمی متعدد، به لوكوسيتها و فرآورده‌های حاصل از آنها اشاره مي‌نمايند كه اثرات معني‌داري بر اسپرم و عملكرد آن دارند. از این رو تشخیص لوکوسیتواسپرمی، علل ایجادکننده و درمان آن جایگاه ویژه‌ای در بررسی زوج‌های نابارور دارد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Leukocytes in the male genital tract and seminal fluid play a complex and dynamic role. Leuko-cytes are found in virtually every ejaculate and function at multiple levels. Presence of high leuko-cyte counts in seminal fluid is an important indicator of male genital tract infection or inflamma-tion. In many studies, leukocytospermia has been associated with male infertility. Decreased sperm count and motility, as well as increased abnormal sperm morphology and a high frequency of immature germ cells, have been reported in men with leukocytospermia. According to the World Health Organization, leukocytospermia is defined as the presence of 1 x 106 WBCs per milliliter of semen. Methodological problems have been found to interfere in differentiating WBCs from immature germ cells that are present in the seminal fluid. For clinical purposes, peroxidase staining is the most practical method of leukocyte detection in semen. 
A large number of studies have shown a wide range of leukocytospermia incidence in infertile men (from 2% to 35%). The majority of studies with the largest number of cases have estimated the prevalence of leukocytospermia to be between 12 and 20% among all infertile men. 
The assumption that leukocytospermia is merely the result of a subclinical male genital tract infec-tion is not correct. Environmental factors such as smoking, alcohol consumption, and marijuana use, increase the number of WBCs in semen. Prolonged abstinence and certain sexual practices, such as anal sex, may also cause leukocytospermia. Nowadays, numerous scientific evidences refer to leukocytes and their products as effective factors on sperm and their functions. It is thus strongly believed that diagnosis of leukocytospermia and its causative agents as well as its treat-ment play a crucial role in evaluation of infertile couples.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>401</FPAGE>
            <TPAGE>411</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Hooman</Name>
<MidName>H</MidName>
<Family>Sadri-Ardekani</Family>
<NameE>هومن </NameE>
<MidNameE></MidNameE>
<FamilyE>صدری‌اردکانی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Mehdi</Name>
<MidName>MM</MidName>
<Family>Akhondi</Family>
<NameE>محمدمهدی</NameE>
<MidNameE></MidNameE>
<FamilyE>آخوندی</FamilyE>
<Organizations>
<Organization>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</Organization>
</Organizations>
<Universities>
<University>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>akhondi@avicenna.ac.ir</Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Leukocytospermia</KeyText></KEYWORD><KEYWORD><KeyText>Infertility</KeyText></KEYWORD><KEYWORD><KeyText>Peroxidase</KeyText></KEYWORD><KEYWORD><KeyText>Seminal fluid</KeyText></KEYWORD><KEYWORD><KeyText>WBCs</KeyText></KEYWORD><KEYWORD><KeyText>Urogenital tract infections</KeyText></KEYWORD>
    </KEYWORDS>
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    <REFRENCES>
        <REFRENCE>
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