<?xml version="1.0" encoding="utf-8" ?>

<XML>
  <JOURNAL>   
    <YEAR>2006</YEAR>
    <VOL>7</VOL>
    <NO>1</NO>
    <MOSALSAL>26</MOSALSAL>
    <PAGE_NO>75</PAGE_NO>  
    <ARTICLES>

<ARTICLE>
    <TitleF>تأثير ماتريژل بر روند تكاملي بلاستوسيست موش</TitleF>
    <TitleE>The effects of Matrigel on the developmental processes of mouse blastocysts</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: كشت جنين روي ماتريژل، يكي از روش‌هاي مناسب بررسي تكامل جنين در محيط آزمايشگاه مي‌باشد. البته به‌كارگيري محيط‌هاي متفاوت كشت همراه با آن و همچنين تفاوت در مراحل تكاملي جنين، مي‌تواند منجر به پديد آمدن نتايج متفاوتي در مطالعات شود. از آنجايي كه استفاده از ماتريژل در مورد تمام گونه‌ها و در مراحل مختلف تكاملي جنين مورد بررسي قرار نگرفته است، مطالعه حاضر به منظور بررسي اثر ماتريژل بر روند تكاملي بلاستوسيست‌هاي جمع‌آوري شده موش صورت گرفت. 
مواد و روشها: به موش‌های ماده نژاد NMRI هورمون‌های hMG و hCG براي تحريك‌ تخمك‌گذاري تزريق شد. سپس موش‌هاي ماده با موش‌های نر از همان نژاد جفت‌‌گيری نمودند. بلاستوسيست‌هاي حاصل، به دو گروه 150 عددي برای گروه آزمايش و گروه 134 عددي برای گروه کنترل تقسيم شدند. بلاستوسيستها به مدت 48 ساعت در محيط کشت M16 داراي BSA  به ميزانmg/ml 4 کشت داده شدند و با بلاستوسيست‌های کشت شده در ماتريژل همراه با محيط مشابه ((M16 +4mg/ml BSA مقايسه شدند. روند تکاملی هر 24 ساعت تا 48 ساعت مطالعه شد. نتايج حاصل با استفاده از آزمون 2 و نرم افزار آماري SPSS تجزيه و تحليل شد.
نتايج: بعد از گذشت 24 ساعت از كشت، درصد بلاستوسيست‌هاي گروه آزمايش كه به مرحله بلاستوسيست‌های جوانه‌زده مرحله اول رسيدند (74%)، در مقايسه با گروه كنترل (2/52%)، به‌طور معني‌داري (05/0&gt;p) بيشتر بود اما درصد بلاستوسيست‌هاي فراگمنته در گروه كنترل 9/11% بود كه تفاوت معني‌داري (05/0&gt;p)، با گروه آزمايش (2%) داشت. بعد از 48 ساعت از کشت 41% از بلاستوسيست‌هاي كشت داده شده در گروه کنترل، به مرحلة بلاستوسيست‌هاي جوانة زده مرحلة اول پيشرفت نمودند و اين ميزان بالاتر از درصد بلاستوسيست‌هاي اين مرحله در گروه آزمايش بود (05/0&gt;p). همچنين درصد بلاستوسيست‌های جوانه‌زده مرحله دوم، در گروه آزمايش بعد از 48 ساعت (78%)، با اختلاف معني‌دار (05/0&gt;p)، نسبت به گروه کنترل (59%) بالاتر بود.
نتيجه‌گيری: اين مطالعه نشان داد كه بلاستوسیست‌های کشت داده شده بر روی ماتريژل همراه با محيط كشت غني شده M16 حاوي BSA (mg/ml 4) در مقایسه با بلاستوسيست‌هايی که در محيطM16  حاوي BSA (mg/ml4) کشت داده شدند، تكامل و رشد بیشتری دارند. بررسي فراساختمانی جنينها و يا بررسي‌هاي ايمونوسيتوشيميايي در تكميل يافته‌هاي اين مطالعه پيشنهاد مي‌شود.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Culturing embryos on Matrigel™, is one of the most suitable methods for study-ing in vitro embryonic developments. As Matrigel has not been used extensively in different species for embryonic development studies, this study was undertaken to determine the effects of Matrigel on the developmental processes of mouse blastocysts. 
Materials &amp; Methods: To a number of female NMRI mice, hMG and HCG injections were made for ovulatory stimulation and then they mated with males from the same strain. Later on, blastocysts were obtained and randomly divided into 2 groups: 150 case blastocysts and 134 control blastocysts. Blastocysts were cultured for 48 hours in M16 medium, supplemented with 4mg/ml of bovine serum albumin (BSA). Later, the blastocysts were compared with the blastocysts cultured in Matrigel plus the same medium. Developmental studies were carried out every 24 hours for 2 days. The data was analyzed by SPSS software and the results were tested by chi-squared. 
Results: After 24 hours, a significantly higher ratio of embryos reached the hatched blastocysts stage Ι in the case group (74%), compared with that of the control group (52.2%), (p&lt;0.05). At the same time the percentage of fragmented blastocysts in the control group was 11.9% which was significantly higher than the case group (2%), (p&lt;0.05). After 48 hours, 41% of blastocysts cultured in the control medium, developed to stage I, the value being significantly more than the blastocysts in the case group (p&lt;0.05). Moreover, after the same period of time (48 hours), the percentage of stage II hatched blastocysts in the case group (79%) was higher than the control groups (59%), (p&lt;0.05).
Conclusion: Matrigel use in enriched culture media can increase development and growth of mouse blastocysts. It also seems that ultrastructural studies of cultured embryos or immunocyto-chemical studies from this regard would be beneficial in understanding the processes involved.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>07</FPAGE>
            <TPAGE>17</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Mariya</Name>
<MidName>M</MidName>
<Family>Zahiri</Family>
<NameE>ماریا</NameE>
<MidNameE></MidNameE>
<FamilyE>زهیری</FamilyE>
<Organizations>
<Organization>Histology Department, Faculty of Medicine, Tabriz Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Histology Department, Faculty of Medicine, Tabriz Medical Sciences University</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>mghaffarin@yahoo.com</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Behrooz</Name>
<MidName>B</MidName>
<Family>Niknafs</Family>
<NameE></NameE>
<MidNameE></MidNameE>
<FamilyE></FamilyE>
<Organizations>
<Organization>Laboratory of Histology &amp;amp; Cellular Biology, Drug Applied Research Center, Tabriz University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Laboratory of Histology &amp; Cellular Biology, Drug Applied Research Center, Tabriz University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><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></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Blastocyst</KeyText></KEYWORD><KEYWORD><KeyText>Culture media</KeyText></KEYWORD><KEYWORD><KeyText>Matrigel</KeyText></KEYWORD><KEYWORD><KeyText>Embryo Development</KeyText></KEYWORD><KEYWORD><KeyText>Laboratory mouse</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>219.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Ben-Rafael Z., Benadiva C.A., Ausmanas M., Barber B., Blasco L., Flickinger G.L., Masteroianni L. Dose of human menopausal gonadotropin influences the out-come of an invitro fertilization program. Fertil Steril. 1987;48:964.##Kathy L., Sharpe T., Randall L.Z. Oocyte and pre- embryo classification. In the handbook of Assisted Reproduction Laboratory. Keel B.A., May J.V., De Jonge C.J. (Editors). 1st Edition, CRC Press, Florida. 2000;pp:188-193.##de los Santos M.J., Mercader A., Galan A., Albert C., Romero J.L., Pellicer A. Implantation rates after two, three or five days of embryo culture. Placenta.2003;24: (suppl):S13-9.##Quinn P., Kerin J.F., Warnes G.M. Improved pregnan-cy rate in human in vitro fertilization with the use of a medium based on the composition of human tubal fluid. Fertil Steril.1985;44(4):493-8.##Trew A.J., Lash G.E., Baker P.N. Investigation of an In Vitro model of trophoblast invasion. Biol Med.2000; 4(3):176-190.##غفاری معرفت، آخوندی محمد مهدی، حیدری مهناز. بررسی اثرات محیط‌های کشت مختلف بر تکامل جنین و سلول‌های اپی‌تلیال لوله رحم انسان. فصلنامه باروری و ناباروری: سال چهارم(1381)، شماره1، صفحات 16-5.##Campbell S., Rowe J., Jakson C.J., Gallery E.D.M. In vitro migration of cytotrophoblasts through a decidual endothelial cell monolayer. Placenta.2003;24:306-315.##Murphy C.R. Uterine receptivity and the plasma memb-rane transformation. Cell Res.2004;14(4):259-267.##Lazzaroni L., Fusi F.M., Doldi N., Ferrrari A. The use of Matrigel at low concentration enhances in vitro blastocyst formation and hatching in a mouse embryo model. Fertil Steril.1999;71(6):1133-1137.##Dawson K.M., Baltz J.M., Claman P. Culture with Matrigel inhibits development of mouse zygotes. J Assist Reprod Genet.1997;14(9):543-8.##Edashing K., Asano A., An T.Z., Kasai M. Restora-tion of resistance to osmotic swelling of vitrified mouse embryos by short term culture. Cryobiology. 1999;38(4):273-80.##Baharvand H., Valojerdi M.R. Effect of glucose and phosphate on the development of one-cell NMARI mouse embryo in M16, CZB and T6 media. Physiol  Pharmacol.1999;3(1).##Goldman- Wohl D.G., Yagel S. Regulation of tropho-blast invasion: from normal implantation to pre- eclampsia. Mol Cell Endocrinol.2002;187(1-2):233-8.##Spenceer T.E., Johnson G.J., Bazar F.W., Burghart R. C. Implantation mechanism: insights from the sheep. Reproduction.2004;128:657-668.##Carson D.D., Bagchi I., Dey S.K., Enders A.C., Fazle-bas A.T. Review embryo implantation. Dev Biol.2000; 223:217-237.##Desai N., Lawson J., Scarrow M., Kinzer D., Goldfarb J. Evaluation of the effect of interlukin-6 and human extracellular matrix on embryonic development. Hum Reprod.1999;14(6):1588-1592.##Carver J., Martin K., Spyropoulou I., Barlow D., Sargent I., Mardon H. An in-vitro model for stromal invasion during implantation of the human blastocyst. Hum Reprod.2003;18(2):283-290.##Armant D.R., Kameda S. Mouse trophoblast cell invasion of extracellular matrix purified from endomet-rial tissue: a model for peri-implantation development. J Exp Zool.1994;269(2):146-56.##Karja N.W.K., Otoi T., Murakami M., Yuge M., Fahrudin M., Suzuki T. Effect of protein supplement to the hatching and hatched blastocyst stage of  cat IVF embryo. Reprod Fertil Develop.1996;14(5):291-296.##Menino A.R., Oclaray J.L. Enhancement of hatching and trophoblastic outgrowth by mouse embryos cultured in Whittens medium containing plasmin and plasminogen. J Reprod Fertil.1986;77:159-167.##Sakkas D., Urner F., Menezo Y., Leppens G. Effect of glucose and fructose on fertilization, cleavage and viability of mouse embryos in vitro. Biol Reprod. 1993;49:1288-1292.##Loutradis D., Drankakis P., Kalliandis K., Sofikitis N., Kallipolitis G., Millingos S., Makris N., Michalas S. Biological factors in cultuer media affecting in vitro fertilization, preimplantation embryo development, and implantation. Ann NY Acad Sci.2000;900:325-35.##Scott L.A. Oocyte and embryo culture. In the handbook of Assisted Rep-roduction Laboratory. Keel B.L., May J.V., De Jonge C.J. (Editors). 1st Edition, CRC Press, Florida.2000;pp:197-220.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>ارزيابي تغييرات فعاليت آنزيم اسيد فسفاتاز تخمدان موش طي ابتداي دوران بارداري طبيعي و كاذب تا زمان لانه‌گزيني</TitleF>
    <TitleE>Evaluation of acid phosphatase activity alterations in mouse ovary after ovarian hyperstimulation in early stages of pseudo and normal pregnancies until implantation time</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: آنزيم اسيد فسفاتاز يك آنزيم ليزوزومي است كه در فعاليت‌هاي متابوليكي تخمدان مانند بلوغ تخمك، از سرگيري مجدد تقسيم ميتوز، شكستن ژرمينال وزيكول و پديده تخمك‌گذاري نقش دارد و همچنين با فعاليت اتوفاژي و هتروفاژي باعث هضم جسم زرد و فوليكول آترتيك مي‌شود. با توجه به اينكه اين آنزيم توسط هورمون استروئيدي كنترل مي‌شود، اين مطالعه براي بررسي الگوي تغييرات فعاليت اين آنزيم در تخمدان موش پس از تحريك تخمك‌گذاري با استفاده از تزريق گنادوتروپين‌هاي PMSG و hCG نسبت به گروه شاهد طي دوران ابتداي حاملگي طبيعي و كاذب طراحي گرديد. 
روش بررسي: موش‌هاي ماده نژاد NMRI با سن بين 10-6 هفته انتخاب و به‌طور تصادفي به دو گروه شاهد و تحريك شده (با به كارگيري PMSG و hCG) تقسيم شدند. سپس هر گروه نيز به دو گروه باردار به روش طبيعي و باردار كاذب تقسيم گرديدند. جهت القاي بارداري كاذب از تحريك مكانيكي واژن استفاده شد. در هر گروه روزانه 5 سر موش از روز اول تا ششم به طريق جابجايي مهره‌هاي گردني كشته شدند و به منظور ارزيابي‌هاي بيوشيميايي، هر دو تخمدان آنها جدا و پس از هوموژن نمودن و سانتريفوژ كردن با دور g 14000 استخراج بافتي در معرض سوبستراي پارانيتروفنيل فسفات قرار گرفت و فعاليت آنزيم برحسب IU/dl محاسبه و پس از تعيين مقدار پروتئين نمونه‌ها برحسب واحد mg/dl ، فعاليت اختصاصي ACP برحسب واحد IU/mg محاسبه شد. داده‌هاي تحقيق حاضر با استفاده از آزمون Mann Whitheny مورد تجزيه و تحليل قرارگرفت. اختلاف آماری در سطح 05/0p&lt; معني‌دار در نظر گرفته شده و به صورت ميانگين خطای استاندارد تعريف گرديد. براي بررسي‌هاي هيستوشيميايي، يکي از تخمدانها انتخاب و با استفاده از دستگاه كرايوستات، برش‌هايي به ضخامت m5 تهيه شد. سپس برشها طبق روش گوموري، رنگ‌آميزي شدند. 

نتايج: فعاليت اختصاصي آنزيم ACP در نمونه‌هاي بافتي تخمدان در گروه‌های شاهد بارداري طبيعي، شاهد بارداري 
كاذب، تحريک بارداري طبيعي و تحريک بارداري کاذب در روز اول به ترتيب شامل IU/mg 12/034/0، IU/mg 04/039/0، IU/mg 08/040/0، IU/mg 01/045/0 و در روز چهارم به ترتيب شامل IU/mg 10/069/0، IU/mg 065/061/0، IU/mg 10/009/1، IU/mg 05/079/0 بود. تغييرات فعاليت آنزيم تخمدان در مطالعات بيوشيميايي با نتايج به‌دست آمده در بررسي‌هاي هيستوشيميايي در كليه گروهها مطابقت داشت. يافته‌هاي حاصل نشان داد كه بيشترين تغييرات فعاليت آنزيم در سلول‌هاي گرانولوزا بود به طوريکه در کليه گروهها حداقل فعاليت آنزيم در روز اول حاملگي (0) و حداکثر آن در روز چهارم (3+) ديده شد.
نتيجه‌گيري: در مجموع نتايج اين تحقيق نشان داد كه افزايش فعاليت آنزيم اسيد فسفاتاز در روزهاي سوم و چهارم بارداري مؤيد نقش اين آنزيم در فرايندهاي متابوليکي تخمدان و استروئيدسازي است و همچنين تحريك تخمك‌گذاري نمي‌تواند باعث تغييرات مشخصي در الگوي فعاليت آنزيم ACP تخمدان طي بارداري اوليه شود، هر چند كه به مطالعات بيشتري در اين زمينه نياز است.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Acid phosphatase (ACP) is a lysosomal enzyme which contributes in ovarian metabolic functions such as oocyte maturation, resumption of mitotic divisions, germinal vesicle breakdown and ovulation. It digestes the corpus lutetium and helps the atresia of follicles by autophagia and hetrophagia activities. Considering the hormonal control of this enzyme, the present study was designed to deterimine the ovarian ACP activity after ovulation stimulation by the administration fo PMSG and hCG during preimplantation period. 

Materials &amp; Methods: For this purpose a number of 6 to 10-week old female NMRI mice were selected and randomly divided into control and hyperstimulated groups after the administeration of PMSG and hCG, and later to pregnant and pseudopregnant groups. The mice were rendered pseudopregnant by mechanical vaginal stimulatin. Five mice in each group were sacrificed by cervical dislocation at the first to the sixth day of pregnancy for biochemical assays. The ovarian samples were obtained and were hemo-genated and centrifuged at 14000 g. The activity of the enzyme was determined using paranitrophenyl phosphate as substrate and later the specific activity of the enzyme was calculalated according to the amount of total protein. The data were analysed by Mann Whitheny test. Statistical significance was indicated by a P value less than 0.05. For hisotchemical evaluations, the sampels were obtained from one of the ovaries in each mouse and then 5 m thick cryosections were prepared. Cryosections were stained by Goumory method. 

Results: The ACP activity of ovarian tissues in the first day of pregnancy in the normal pregnant and pseudopregnant control groups, hyperstimulated normal pregnant and pseudopregnant groups were 0.340.04 IU/mg, 0.390.04 IU/mg, 0.40.08 IU/mg, 0.450.01 IU/mg respectively and in the fourth day were 0.690.1 IU/mg, 0.61 0.06 IU/mg, 1.090.10 IU/mg and 0.79 0.05 IU/mg. The results showed that biochemical findings correlated with histochemical observations. The ACP reaction changes were seen mainly in granulosa cells with a minimum enzyme activity in the first day (zero activity) and a maximum activity in the fourth day of pregnancy (+3).

Conclusion: The increased ACP activity on the 3rd- 4th days of pregnancy, may be due to the este-roidogenic activity of granulosa cells. Also, the results showed that ovarian hyperstimulation could not change the pattern of ovarian ACP activity during early stages of pregnancy. More research is required in this area for a better understanding of the processes.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>17</FPAGE>
            <TPAGE>25</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Maryam</Name>
<MidName>M</MidName>
<Family>Nazm Bojnordi</Family>
<NameE>مریم</NameE>
<MidNameE></MidNameE>
<FamilyE>نظم بجنوردی</FamilyE>
<Organizations>
<Organization>Anatomy Department, Faculty of Medical Sciences, Tarbiyat Modares University</Organization>
</Organizations>
<Universities>
<University>Anatomy Department, Faculty of Medical Sciences, Tarbiyat Modares University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mojdeh</Name>
<MidName>M</MidName>
<Family>Salehnia</Family>
<NameE>مژده</NameE>
<MidNameE></MidNameE>
<FamilyE>صالح نیا</FamilyE>
<Organizations>
<Organization>Anatomy Department, Faculty of Medical Sciences, Tarbiyat Modares University</Organization>
</Organizations>
<Universities>
<University>Anatomy Department, Faculty of Medical Sciences, Tarbiyat Modares University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>mghaffarin@yahoo.com</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Abdolamir</Name>
<MidName>A</MidName>
<Family>Allameh</Family>
<NameE>عبدالامیر</NameE>
<MidNameE></MidNameE>
<FamilyE>علامه</FamilyE>
<Organizations>
<Organization>Department of Biochemistry, Medical Faculty, Tarbiat Modarres University</Organization>
</Organizations>
<Universities>
<University>Department of Biochemistry, Medical Faculty, Tarbiat Modarres University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Acid phosphatase</KeyText></KEYWORD><KEYWORD><KeyText>Ovulation induction</KeyText></KEYWORD><KEYWORD><KeyText>Ovary</KeyText></KEYWORD><KEYWORD><KeyText>Implantation</KeyText></KEYWORD><KEYWORD><KeyText>Pseudopregnancy</KeyText></KEYWORD><KEYWORD><KeyText>Preimplantation</KeyText></KEYWORD><KEYWORD><KeyText>Esteroidogenesis</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>220.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Brayman M., Thathiah A., Carson D. MUCI: A multi-functional cell surface component of reproductive tissue epithelial. Reprod Biol.2004;2: 4-8.##Aplin J.D. The cell biological basis of human implan-tation. Obstet Gynecol.2000;14:757-764.##Tsiligiann T.H., Karagiannidis A., Saratsis P., Brikas P. Enzyme activity in bovine cervical mucus during spon-taneous and induced estrus. J Vet Res.2003;67:189-93.##Bull H., Murray P., Thomas D., Fraser A., Nelson P. Acid phosphatase. J Clin Pathol.2002;55:65-72.##Flood P.F., Tyler N.J.C., Read E.K., Rodway M.J., Chedrese P.J. Ovarian and placental production of pro-gesterone and oestradiol during pregnancy in reindeer. Anim Reprod Sci.2005;85:147-162.##Cheema R., Dhanju C.K., Matharoo J.S. Response rela-ted enzymatic changes in ovaries of superovulated mice. Exp Biol.2003;41(2):171-173.##Imai K., Khandoker M., Yonai M., Takashashi T., Sato T., Ito A. Matrix metalloproteinases-2 and- 9 activities in bovine follicular fluid of differentsized follicles: relationship to intrafollicular inhi-bin and steroid con-centrations. Domest Anim Endocrinol.2003;24:171-83.##Havelok J., Rainey W., Carr B. Ovarian granulosa cell lines. Mol Cell Endocrinol.2004;228:67-78.##Wang I., Fraser I. Lysosomes: An important mediator in the female reproductive tract. Obstet Gynecol.1989; 45(1):18-33.##Kleinman D., Insler V., Leiberman J., Glezerman M., Albotiano S., Potashnik G., et al. Acid phosphatase levels in follicular fluids following induction of ovula-tion in in vitro fertilization patients. J In Vitro Fert Embryo Transf.1987;4(3):181-4.##Banos M.E., Rosales A.M., Ballesteros L.M., Hrnan-dez O., Rosado A. Changes in lysosomal enzyme acti-vities in pre-ovulatory follicles and endometrium of PMSG superovulated rats. Arch Med Res.1996;27(1): 49-55.##Tavanioton A., Albano A., Smitz J., Devroey P. Im-pact of ovarian stimulation on corpus luteum function and embryonic implantation. J Reprod Immunol.2002; 55:123-30.##Rosales T., Avalos R., Vergara O., Hernandez P., Ballesteros L., Garcia M. Multiparametric study of atresia in ewe antral follicle: histology, flow cytomet-ry, internucleosomal DNA fragmentation, and lysoso-mal enzyme activities in granulosa cells and follicular fluid. Mol Reprod Dev.2000;55 (3):270-81.##Beckman G., Beckman L., Lofstrand T. Acid and alkaline phosphatase in amniotic fluid in normal and complicated pregnancy. Act Obstet Gynecol.1978;57: 1-5.##Lindhard A., Ley U., Ravn V., Islin H., Hviid T., Rex .S, et al. Biochemical evaluation of endometrial func-tion at the time of implantation. Fertil Steril.2002;78 (2):221-233.##Wang I., Fraster I., Barsamian S., Monconi F., Street D., Cornillie F., et al. Endometrial lysosomal enzyme activity in ovulatory dysfunctional uterine bleeding, IUCD users and post-partum women. Mol Hum Reprod.2000;6 (3):258-263.##Krajni M., Lenhardt L., Valocky L., Cigankova V., Kostecky M., Maragek I. Activity of alkaline and acid phosphatase and non specific esterase in the endomet-rium and oviduct of post partum does. Elsevier, 2003.##Rosales T., Avalos R., Vergara O., Hernandez P., Ballesteros L., Garcia M. Multiparametric study of atresia in ewe antral follicle: histology, flow cytometry, internucleosomal DNA fragmentation, and lysosomal enzyme activities in granulosa cells and follicular fluid. Mol Reprod Dev.2000;55(3): 270-81.##Bucci M., Murphy C.R. Hormonal control of enzyme activity during the plasma membrane transformation of uterus epithlial cells. Cell Biol. 2001;25(9):859-871.##Henderson K.A., Cupps P.T. Acid and alkaline phos-phatase in bovine antral follicles. Nat Sci.1989;13: 1363-1369.##Ertzeid G., Storeng R. The impact of ovarian stimula-tion on implantation and fetal development in mice. Hum Reprod.2001;16(2):221-225.##Dhanju C.K., Sangha G.K., Sekhon P.K. Biochemical status of ovaries after induction of superovulation on different days of estrus cycle in mice. Ind J Exp Biol. 2001;39(8):777-80.##Lindhim S., Sauer M., Carmina E., Chang P., Zim-merman R., Rogerio A. Circulating levels during ovu-lation induction: relation to adiposity and ovarian mor-phology.Fertil Steril.2000;73(3):493-498.##Emadi M., Salehnia M. The morphological expression of endometrial pinopodes during implantation in mice after ovarian stimulation and pro-gesterone injection. Yakhteh.2004;5(20):140-145.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>مطالعه مورفولوژي و مورفومتری بیضه موش بالغ بدنبال تجویز مقادیر مختلف بوسولفان</TitleF>
    <TitleE>A morphologic and morphometric study of adult mouse testis following different doses of busulfan administration</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: داروهاي ضد سرطان مي‌توانند باعث اختلال اسپرماتوژنز شوند. آگاهي از نحوه عمل آنها براي جلوگيري از تخريب اپیتلیوم ژرمینال ضروري است. با توجه به اينكه یافته‌های کمی می‌توانند پاسخ مهمی برای سوالاتی در زمینه فیزیولوژی بیضه و همچنین کمک موثری برای درک بهتر و کاملتر اسپرماتوژنز باشند مطالعه حاضر با هدف بررسی مورفولوژیك و مورفومتریك بيضه، حجم و دانسیته حجمی پارامترهای بیضه، اندازه‌گیری اقطار لوله سمینیفروس و مطالعه کمی سلول‌های ژرمينال و سوماتیک در بیضه موش بدنبال تجویز دوزهای مختلف بوسولفان انجام گرفت.
روش بررسي: در مطالعه حاضر 42 موش نژاد NMRI با سن 8-6 هفته مورد آزمایش قرار گرفتند. حیوانات به 5 گروه تقسیم شدند. حیوانات در گروه‌های آزمایش اول، دوم، سوم و چهارم به ترتیب یک دوز mg/kg 5، 10، 20، 40 بوسولفان و حیوانات کنترل فقط حلال بوسولفان را به صورت داخل صفاقی دریافت نمودند. پس از گذشت 35 روز، حیوانات را کشته و از بیضه آنها نمونه‌برداری شد. نمونه‌ها جهت بررسی با میکروسکوپ نوری تحت پاساژ و رنگ‌آمیزی قرار گرفتند. سپس مطالعات مورفومتریك بیضه انجام شد و پس از آن، جهت تحليل داده‌ها از آناليز يكطرفه استفاده شد و 05/0p&lt; به‌عنوان سطح معني‌داري در نظرگرفته شد. 
نتايج: نتاج اين مطالعه نشان داد که تجویز بوسولفان در هر سه دوز mg/kg 20،10 و 40 می‌تواند عمده پارامترهای مورفومتریك بیضه را کاهش دهد و با افزایش دوز، این اثرات واضح‌تر و شدیدتر می‌گردد. حجم بیضه، توبولها و اپیتلیوم ژرمینال در گروه‌های آزمایش به طور معني‌دار کاهش (05/0p&lt;) و حجم و دانسیته حجمی بافت بینابینی افزایش یافت (05/0p&lt;). قطر توبولها و ضخامت اپیتلیوم ژرمینال در گروه‌های آزمایش به طور معنی‌داري کاهش نشان داد، ضمن این که قطر مجاري سمي‌نيفروس داراي افزایش بود (001/0p&lt;). در شمارش سلولی، تمام سلول‌های ژرمينال کاهش داشتند؛ در حالی که تعداد سلول‌های سرتولی دچار تغییر نگرديده بود. تعداد سلول‌های لیدیگ در گروه‌های تحت درمان با mg/kg 10و 20 تغییري نداشت؛ ولي در گروه تحت درمان با mg/kg 40، تعداد آنها به طور معنی‌دار افزایش یافت (01/0p&lt;). در گروه تحت درمان با mg/kg 5 چه از نظر مورفولوژی و چه از نظر مورفومتری تغییر خاصی در بافت بیضه مشاهده نشد. 
نتیجه‌گیری: بوسولفان از طریق تأثیر بر سلول‌های ژرمينال و سوماتیک موجود در بیضه می‌تواند در تخریب اسپرماتوژنز و کاهش پارامترهای بیضه نقش داشته باشد و اثرات آن به صورت وابسته به دوز افزایش یابد. بنابراین ضمن استفاده از این دارو در بیماران سرطانی این عارضه نیز باید مدنظر قرار گیرد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Anti-cancer drugs have adverse effects on spermatogenesis. Therefore, informa-tion on their role for the prevention of germinal epithelium destruction is necessary. The aim of this study was morphologic and morphometric evaluations of testes, measurement of volume and volume density of testes parameters, measurement of tubular diameters, germ and somatic cell counts following administration of different doses of busulfan in adult mice.
Materials &amp; Methods: In the present study, 42 male NMRI mice aged 6-8 weeks were used. The animals were divided into 5 groups. Case groups received a single dose of busulfan by intraperitoneal injection as 5, 10, 20 and 40 mg/kg in the first, second, third and forth groups respectively. The control group received only the solvent for busulfan. All the animals were killed 35 days after treatment and their testes were dissected out and processed for light microscope studies. Then morphometric studies were performed on testicular parameters. The data were analyzed using ANOVA and Tukey test and p values less than 0.05 were considered significant.
Results: Busulfan administration in 5, 10, 20 and 40 mg/kg doses significantly reduced most morphometric parameters in testes with a maximum effect in the 40 mg/kg group. Volumes of testes, tubules and germinal epithelia were decreased significantly in the experiment groups (p&lt;0.05) however, the volume of interstitial tissue increased (p&lt;0.05). Tubular diameters and thickness of epithelia were also decreased in the experiment groups. Number of germ cells was reduced, but number of sertoli cells was not affected. The number of leydig cells were not affected in 10 and 20 mg/kg busulfan treated groups, however in the 40 mg/kg treated group they were increased significantly (p&lt;0.003). In 5 mg/kg treated group there were no significant differences in morphologic and morphometric studies.
Conclusion: Busulfan could reduce testicular parameters and disrupt spermatogenesis through affecting both germ and somatic cells in a dose dependent manner. Therefore, the side effects of busulfan on spermatogenesis should be considered during cancer therapies.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>25</FPAGE>
            <TPAGE>37</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Mohammad Amin</Name>
<MidName>MA</MidName>
<Family>Homafar</Family>
<NameE>Mohammad Amin</NameE>
<MidNameE></MidNameE>
<FamilyE>Homafar</FamilyE>
<Organizations>
<Organization>Faculty of Medicine, Tabriz University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Faculty of Medicine, Tabriz University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>ghasemi.histolab@gmail.com</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Jafar</Name>
<MidName>J</MidName>
<Family>Soleimanirad</Family>
<NameE>جعفر</NameE>
<MidNameE></MidNameE>
<FamilyE>سلیمانی راد</FamilyE>
<Organizations>
<Organization>Histology Department, Faculty of Medicine, Tabriz Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Histology Department, Faculty of Medicine, Tabriz Medical Sciences University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Ahmad Ali</Name>
<MidName>AA</MidName>
<Family>Ghanbari</Family>
<NameE>احمد علی</NameE>
<MidNameE></MidNameE>
<FamilyE>قنبری</FamilyE>
<Organizations>
<Organization>Department of Anatomy, Faculty of Medicine, Tabriz University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Department of Anatomy, Faculty of Medicine, Tabriz University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Spermatogenesis</KeyText></KEYWORD><KEYWORD><KeyText>Busulfan</KeyText></KEYWORD><KEYWORD><KeyText>Morphometry</KeyText></KEYWORD><KEYWORD><KeyText>Mouse</KeyText></KEYWORD><KEYWORD><KeyText>Testis</KeyText></KEYWORD><KEYWORD><KeyText>Chemotherapy</KeyText></KEYWORD><KEYWORD><KeyText>Germ cells</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>221.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
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A long medical book Katzung &amp; Trevors Pharmacology exa-mination and board review. Mc Graw Hill.2002;6th Edition.pp:206-8.##Molenaar R., de Rooij D.G., Rommerts F.F, Reuvers P. J., van der Molen H.J. Specific destruction of Leydig cells in mature rats after in vivo administration of ethane dimethyl sulfonate. Biol Reprod.1985;33(5): 1213-22.##Boujrad N., Hochereau-de Riviers M.T., Kamtchouing P., Perreau C., Carreau S. Evolution of somatic and germ cell populations after busulfan treatment in utero or neonatal cryptorchidism in the rat. Andrologia. 1995;27(4):223-8.##Jansz G.F., Pomerantz D.K. The effect of prenatal treatment with busulfan on in vitro androgen produc-tion by testes from rats of various ages. Can J Physiol Pharmacol.1985;63(9):1155-8.##Brinster R.L., Avarbock M.R. Germline transmission of donor haplotype following spermatogonial trans-plantation Proc Natl Acad Sci USA.1994;91:11303-7.##Honaramooz A., Behboodi E., Hausler C.L., Blash S., Ayres S., et al. Depletion of endogenous germ cells in male pigs and goats in preparation for germ cell trans-plantation. J Androl. 2005;26(6):698-705.##De Sanctis V., Galimberti M., Lucarelli G., Polchi P., Ruggiero L., Vullo C.Gonadal function after allogenic bone marrow transplantation for thalassaemia. Arch Dis Child.1991;66(4):517-20.##Grigg A.P., McLachlan R., Zaja J., Szer J. Reproduc-tive status in long-term bone marrow transplant survi-vors receiving busulfan-cyclophosphamide (120mg/kg) Bone Marrow Transplant.2000;26(10):1089-95.##Afify Z., Shaw P.J., Clavano-Harding A., Cowell C.T. Growth and endocrine function in children with acute myeloid leukaemia after bone marrow transplantation using busulfan/ cyclophosphamide. Bone Marrow Transplant.2000;25(10):1087-1092.##Yang Z.W., Guo Y., Lin L., Wang X.H., Tong J.S., Zhang G.Y. Quantitative (stereological) study of in-complete spermatogenic suppression induced by testos-terone undecanoate injection in rats. Asian J Androl. 2004;6(4):291-7.##Osinubi A.A., Noronha C.C., Okanlawon A.O., Mor-phometric and stereological assessment of the effects of long-term administration of quinine on the morpho-loyg of rat testis. West Afr J Med.2005;24(3):200-5.##Vecino P., Uranga J.A., Arechaga J. Suppression of spermatogenesis for cell transplantation in adult mice. Protoplasma.2001;217(4):191-8.##Aich S., Manna C.K. Histophysiological changes of the testicular tissue due to busulphan administration in the wild Indian house rat. Acta Biol Hung.2001;52 (1):105-16.##Haddad S., Carvalho T.L., Anselmo-Franci J.A., Pete-nusci S.O., Favaretto A.L. Ultrasound stimulation of rat testes damaged by busulfan. Ultrasound Med Biol. 1997;23(9):1421-25.##Bucci L.R., Meistrich M.L. Effects of busulfan on murine spermatogenesis: cytotoxicity, sterility, sperm abnormalities, and dominant lethal mutations. Mutat Res.1987;176(2):259-68.##Mandarim-de-Lacerda C.A. Stereological tools in bio-medical research. An Acad Bras Cienc.2003;75(4):469 -86.##Udagawa K., Ogawa T., Watanabe T., Yumura Y., Takeda M., Hosaka M. GnRH analog, leuprorelin acetate, promotes regeneration of rat spermatogenesis after severe chemical damage. Int J Urol.2001;8(11): 615-22.##Jiang F.X. Behavior of spermatogonia following reco-very from busulfan treatment in the rat. Anat Embryol (Berl).1998;198(1):53-61.##Adler I.D. Comparison of the duration of spermato-genesis between male rodents and humans. Mutar Res. 1996;352(1-2):169-72.##Cheng Yan C., Mruck D.D. Cell junction dynamic in the testis: sertoli-germ cell interaction and male contra-ceptive development. Physiol Rev.2002;82:825-874.##Costa D.S., Paula T.A., Matta S.L. The intertubular compartment morphometry in capybaras (Hydrochoe-rus hydrochaeris) testis. Anim  Reprod  Sci.2006;91(1-2):173-9.##Tae H.J., Jang B.G., Ahn D.C., Choi E.Y., Kang H.S., et al. Morphometric studies on the testis of Korean ring-necked pheasant (Phasianus colchicus karpowi) during the breeding and non-breeding seasons. Vet Res Commun.2005;29(7):629-43.##Gunderson H.J., Bagger P., Bendtsen T.F., Evans S. M, Korbo L., et al. The new stereological tools: disec-tor, fractionator, nucleator and point sampled intercepts and their use in pathological research and diagnosis. APMIS.1988;96(10):857-81.##Hess R.A. Spermatogenesis overview, encyclopedia of reproduction.1999;(4):Academic press University  f Illinois at Urbana.pp:534-45.##Bar-Shira Maymon B., Yogev L., Marks A., Hauser R., Botchan A., Yavets H. Sertoli cell inactivation da-mage to the human testis after cancer chemotherapy. Fertil Stril.2004:81(5):1391-1394.##Shinohara T., Orwig K.E., Avarbock M.R., Brinster R.L., Restoration of spermatogenesis in infertile mice by sertoli cell transplantation. Biol Reprod.2003;68(3): 1064-71.##Choi Y.J., Ok D.W., Kwon D.N., Chung J.I., Kim H.C., et al. Murine male germ cell apoptosis induced by busulfan treatment correleates with loss of c-kit-expression in a Fas/FasL-and P53-independent manner. FEBS Lett.2004;575(1-3):41-51.##Sawhney P., Gimmona C.J., Meistrich M.L., Richburg J.H. Cisplatin- induced long-term failure of spermato-genesis in adult C57/Bl/6J Mice. J Androl.2005;26(1): 136-45.##Cai L., Hales B.F., Robaire B. Induction of apoptosis in the germ cells of adult male rats after exposure to cyclophosphamide. Biol Reprod.1997;56(6):1490-7.##O Donell L., Robertson K.M., Jones M.E., Simpson E.R. Estrogen and spermatogenesis.2001;22(3):289-318.##Siril Ariyaratne H.B., Ian Mason J., Mendis- Handagama S.M. Effects of thyroid and luteinizing hormones on the onset of precursor  cell differentiation into leydig progenitor cells in the prepubertal rat testis. Biol Reprod.2000;63(3):898-904.##Benton L., Shan L.X., Hardy M.P., Differentiation of adult Leydig cells. J Steroid Biochem Mol Biol.1995; 53(1-6):61-8.##Mendis- Mandagama S.M.L., Risbridger G.P., de Kretser D.M. Morphometric analysis of the compo-nents of the neonatal and the adult rat testis intersti-tium. Int J Androl.1987;10:525-534.##Qin D.N., Lung M.A. Morphometric study on leydig cells in capsulotomized testis of rats. Asian J Androl. 2002;4(1):49-53.##Ballester J., Dominguez J., Munoz M.C., Sensat M., Rigau T., et al. Tungstate treatment improves Leydig cell function in streptozotocin- diabetic rats. J Androl. 2005;26(6):706-15.##Howell S.J., Shalet S.M. Testicular function following chemotherapy. Hum Reprod Update.2001;7(4):363-9.##Zhengwei Y., McLachlan R.I., Bremner W.J., Wre-ford N.G. Quantitative (stereological) study of the nor-mal spermatogenesis in the adult monkey (Macaca fa-scicularis). J Androl.1997;18(6):681-7.##Meistrich M.L., Wilson G., Huhtaniemi I. Hormonal treatment after cytotoxic therapy  stimulates recovery of spermatogenesis, Cancer Res.1999;59(15):3557-60.##Tan K.A., Walker M., Morris K., Greig I., Mason J.I., Sharpe R.M. Infant feeding with soy formula milk: effects of puberty progression, reproductive function and testicular cell numbers in marmoset monkeys in adulthood. Hum Reprod.2006;21(4):896-904.##Petersen P.M., Giwercman A., Gundersen H.J., Pak-kenberg B. Efficient and unbiased tools for quantitating laydig and sertoli cells in testes from testes biobsies. Image Anal Stereol.2000;19:113-117.##</REF>
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</ARTICLE>

<ARTICLE>
    <TitleF>اثرات ضديخ‌های مختلف بر ميزان شكست DNA در جنين‌های خوک توليد شده به روش  In vitro</TitleF>
    <TitleE>Influence of cryoprotectants on DNA fragmentation of in vitro produced porcine blastocysts</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: تاکنون از ضديخ‌های زيادی جهت انجماد جنين‌های مرحله قبل از لانه‌گزينی به منظور جلوگيری از تشکيل يخ داخل سلولی استفاده شده است، ولي با اين وجود تعداد زيادي از جنينها پس از ذوب به دلايل مختلفي از جمله نوع ضديخ مورد استفاده و به دنبال آن شكست DNA جنين، در اثر سميت ضديخ از بين مي‌روند. اتيلن‌گليکول، 1و2 پروپانديول و گليسرول ضديخ‌های معمول می‌باشند که به طور وسيعی برای انجماد جنين حيوانات گوناگون و همچنين انسان استفاده مي‌شود. هدف از مطالعه حاضر، بررسی اثرات ضديخ‌های مختلف روی ميزان شكست DNA بلاستوسيست‌های خوک به منظور تعيين ضديخ مناسب برای انجماد جنين خوک بود. 
روش بررسي: تعداد 197 بلاستوسيست خوک به روش In vitro توليد شدند و به طور تصادفي به چهار گروه تقسيم گرديدند. تعداد 40 بلاستوسيست به‌عنوان گروه كنترل به مدت يک ساعت در محلول  PBSبدون ضديخ قرار گرفتند. بقیه بلاستوسيستها در سه گروه متفاوت در معرض 3 نوع محلول ضديخ با غلظت 10% به مدت يک ساعت در يك روش 3 مرحله‌اي در درجه حرارت اتاق قرار گرفتند. به‌طوریکه40 بلاستوسيست در معرض  اتيلن‌گليکول و 40 بلاستوسيست در معرض 1و2 پروپانديول و 40 بلاستوسيست در معرض گليسرول قرار گرفتند. شواهد مورفولوژيك از زنده ماندن بلاستوسيستها پس از 24 ساعت كشت مجدد در گروه‌هاي مختلف در محيط NCSU-37، براساس تشکيل مجدد حفره بلاستوسل به وسيله مشاهده استريوميکروسکوپي با بزرگنمايي 40 برابر ارزيابی گرديد. شاخص ميزان شكست DNA در آنها پس از نشانه‌گذاری با تكنيك TUNEL و رنگ‌آميزي زمينه‌ای با PI مشخص شد. داده‌ها با آناليز واريانس و آزمون تعقيبی فيشر و با كمك نرم افزار Stutview مورد تجزيه و تحليل قرار گرفت و سطح معني‌داري 05/0 در نظر گرفته شد.
نتايج: قرار گرفتن بلاستوسيست‌هاي خوک در معرض ضديخ‌های مختلف، منجر به افزايش تعداد هسته‌هايی با شكست DNA می‌شود. در ضمن، ميزان شاخص شكست DNA در بلاستوسيست‌های دارای بلاستوسل نسبت به بلاستوسيست‌های فاقد بلاستوسل، بدون توجه به نوع ضديخ کمتر بود. 
نتيجه‌گيري: براساس نتايج اين مطالعه در معرض ضديخ قرار گرفتن بلاستوسيست‌های خوک، ميزان شكست DNA را افزايش مي‌دهد و در اين ميان اتيلن‌گليکول کمترين ميزان سميت را دارد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: The aim of the present study was to investigate the effects of different cryoprotectants (CPs) on DNA fragmentation of in vitro produced blastocysts to determine an appropriate cryoprotectant for embryo cryopreservation. Therefore, the precise aims of the study were to assess the toxic effects of different cryoprotectants in terms of survival rate and to evaluate the effects of different CPs on DNA fragmentation in in vitro produced porcine blastocysts. Ethylene glycol, 1,2 propanediol and glycerol are common cryoprotectants widely used for embryo cryopreservation in different animals as well as humans. 
Materials &amp; Methods: 197 porcine blastocysts were produced in vitro and 160 blastocysts were random-ly selected and divided into 4 groups. 40 blastocysts were placed in phosphate buffer solution (PBS) with-out any cryoprotectants for 1 hour in room temperature (23-25C) as the control group. The rest of the blastocysts were exposed to 3 different cryoprotectants (10% solutions) ethylene glycol (EG), 1, 2 pro-panediol (PG) and glycerol (Gly) for 1 hour in a 3- step method in room temperature. The survival rate was assessed after culture in NCSU-37 medium for 24 hours as the proportion of recovered embryos with the reformation of blastocele observed by stereomicroscopy at 40 magnifications. The apoptotic indices were evaluated after staining by TUNEL technique to label apoptotic nuclei and later were counter-stained by propidium iodide (PI) to label all nuclei and were analyzed by fluorescent microscopy. Then, the sur-vival rate was compared with the data obtained from the control group. Through ANOVA and Fishers exact test the data were analyzed while employing StatView software and the level of significance was considered as 0.05%. 
Results: Exposing porcine blastocysts to different cryoprotectants results in an increase in DNA fragmentation, although the apoptotic index in blastocysts with blastocele compared to those without them were lower in the study, disregard of the kind of cryoprotectant. 
Conclusion: It is concluded that CPs can decrease the survival rate of porcine blastocysts by increasing the percentage of DNA fragmentation but EG has the least effect on DNA fragmentation.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>37</FPAGE>
            <TPAGE>45</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Farzad</Name>
<MidName>F</MidName>
<Family>Rajaei</Family>
<NameE>فرزاد</NameE>
<MidNameE></MidNameE>
<FamilyE>رجایی</FamilyE>
<Organizations>
<Organization>Cell Culture Laboratory, Department of Anatomy, Qazvin University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Cell Culture Laboratory, Department of Anatomy, Qazvin University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>frajaei@qums.ac.ir</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Takshij</Name>
<MidName>T</MidName>
<Family>Otoi</Family>
<NameE>تاکشیج</NameE>
<MidNameE></MidNameE>
<FamilyE>اتویی</FamilyE>
<Organizations>
<Organization>Department of Reproduction, Faculty of Veterinary, Yamaguchi University</Organization>
</Organizations>
<Universities>
<University>Department of Reproduction, Faculty of Veterinary, Yamaguchi University</University>
</Universities>
<Countries>
<Country>Japan</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Cryoprotectants</KeyText></KEYWORD><KEYWORD><KeyText>Cytotoxicity</KeyText></KEYWORD><KEYWORD><KeyText>Apoptosis</KeyText></KEYWORD><KEYWORD><KeyText>Pig</KeyText></KEYWORD><KEYWORD><KeyText>DNA fragmentation</KeyText></KEYWORD><KEYWORD><KeyText>Blastocyst</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>222.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Hardy K. Cell death in the mammalian blastocyst. Mol Hum Reprod.1997;3:919-925.##Jurisicova A., Rogers I., Fasciani A., Casper R.F., Varmuza S. Effect of maternal age and conditions of fertilization on programmed cell death during murine preimplantation embryo development. Mol Hum  Reprod.1998;4:139-145.##Levy R.R., Cordonier H., Czyba J.C., Guerin J.F. Apoptosis in preimplantation mammalian embryo and genetics. Ital J Anat Embryol.2001;106:101-108.##Hochachka P.W. Defense strategies against hypoxia and hypothermia. Science.1986;231:234-241.##Gavrieli  Y., Sherman Y., Ben-Sasson S.A. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J Cell Biol. 1992;119(3):493-501.##Yamadori I., Yoshino T., Kondo E., Cao L., Akagi T., Matsuo Y., Minowada J. Comparison of two methods of staining apoptotic cells of leukemia cell lines. Terminal deoxynucleotidyl transferase and DNA polymerase I reactions. J Histochem Cytochem. 1998; 46(1):85-90.##Neuber E., Luetjens C.M., Chan A.W., Schatten G.P. Analysis of DNA fragmentation of in vitro cultured bovine blastocysts using TUNEL. Theriogenology. 2002;57(9):2193-202.##Pampfer S., Vanderheyden I., McCracken J.E., Vesela J., De Hertogh R. Increased cell death in rat blasto-cysts exposed to maternal diabetes in utero and to high glucose or tumor necrosis factor-alpha in vitro. Development.1997;124(23):4827-36.##Emiliani S., Van den Bergh M., Vannin A.S., Bira-mane J., Englert Y. Comparison of ethylene glycol, 1, 2- propanediol and glycerol for cryopreservation of slow-cooled mouse zygotes, 4-cell embryos and blas-tocysts. Hum Reprod.2000;15(4):905-10.##Fahning M.L., Garcia M.A. Status of cryopreservation of embryos from domestic animals. Cryobiology.1992; 29:1-18.##Friedler S., Giudice L.C., Lamb E.J. Cryopreserva-tion of embryos and ova. Fertil Steril.1988;49:743-64.##Marquez-Alvarado Y.C., Galina C.S., Castilla B., Leon H., Moreno-Mendoza N. Evidence of damage in cryopreserved and fresh bovine embryos using the Tunel technique. Reprod Domest Anim.2004;39(3): 141-5.##رجایی فرزاد، سلیمانی‌راد جعفر، نیک‌نفس بهروز، غفاری معرفت. اثرات انجماد شیشه‌ای بر میزان آپوپتوز در مرحله بلاستوسیست. فصلنامه پزشکی باروری و ناباروری، شماره اول، سال پنجم، زمستان 1382، صفحات: 22-14.##Kikuchi K., Kashiwazaki N., Noguchi J., Shimada A., Takahashi R., et al. Developmental competence after transfer to recipients of porcine oocytes Matured, fertilized, and cultured in vitro. Biol Reprod.1999;60: 336-40.##Yuge M., Otoi T., Nii M., Murakami M., Karja N.W., et al. Effects of cooling ovaries before oocyte aspira- tion on meiotic competence of porcine oocytes and of exposing in vitro matured oocytes to ambient tempera-ture on in vitro fertilization and development of the oocytes. Cryobiology.2003;47(2):102-8.##Wyllie A.H., Kerr J.F., Currie A.R. Cell death: the significance of apoptosis. Int Rev Cytol.1980;68:251-306.##Leese H.J., Donnay I., Thompson J.G. Human assis-ted conception: a cautionary tale. Lessons from domes-tic animals. Hum Reprod.1998;4(Suppl):184-202.##Wyllie A.H. Apoptosis: an overview. Br Med Bull. 1997;53:451-465.##Jurisicova A., Varmuza S., Casper R.F. Programmed cell death and human embryo fragmentation. Mol Hum Reprod.1996;2:93-98.##Men H., Monson R.L., Parrish J.J., Rutledge J.J.  Detection of DNA damage in bovine metaphase II oocytes resulting from cryopreservation. Mol Reprod Dev.2003;64:245-250.##Oda K., Gibbons W.E., Leibo S.P. Osmotic shock of fertilized mouse ova. J Reprod Fertil.1992;95:737-747.##Pedro P.B., Zhu S.E., Makino N., Sakurai T., Edashige K., Kasai M. Effects of hypotonic stress on the survival of mouse oocytes and embryos at various stages. Cryobiology.1997;35:150-158.##Brison D.R., Schultz R.M. Apoptosis during mouse blastocyst formation: evidence for a role for survival factors including transforming growth factor alpha. Biol Reprod.1997;56:1088-1096.##Kasai M. Simple and efficient methods for vitrifica-tion of mammalian embryos. Anim Reprod Sci.1996; 42:67-75.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>اثرات تراتوژن لاموتريژين بر جنين موش</TitleF>
    <TitleE>The teratogenic effects of Lamotrigine on mouse fetus</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>مقدمه: يكي از مهمترين عوارض مصرف داروهاي ضد صرع در دوران بارداري افزايش ناهنجاري‌هاي جنيني در نوزادان مي‌باشد. جنين‌هايي كه در معرض استفاده از اين داروها قرار مي‌گيرند ريسك ابتلا به ناهنجاري در آنها 10-7% مي‌باشد در حالي كه اين نسبت در كل جامعه 4-2% است. لاموتريژين يكي از جديدترين داروهاي ضد صرع است كه نسبت به داروهاي ضد صرع قديمي‌تر بر روي عوارض تراتوژنيك آن مطالعه كمتري انجام شده اغلب موارد اين دارو را بدون عوارض تراتوژنيك گزارش كرده‌اند. اخيراً مواردي از ناهنجاري‌زايي اين دارو در انسان گزارش شده است ولي گزارشها كم و متناقض بوده و الگوي خاصي از نوع ناهنجاريها ارائه نشده است. لذا اين تحقيق با هدف تعيين اثرات تراتوژنيك دارو در جنين موش انجام شده است. 

روش بررسي: براي انجام كار موش‌هاي سوري حامله به چهار گروه تقسيم شدند. گروه اول (كنترل 1) هيچ ماده‌اي دريافت نكردند گروه دوم (كنترل 2) حلال اتانول به صورت داخل صفاقي دريافت كردند گروه سوم (مورد 1) mg/kg25 در سه دوز به روش داخل صفاقي دريافت كردند گروه چهارم (مورد 2) mg/kg75 لاموتريژين در سه دوز به روش داخل صفاقي دريافت كردند. شروع تزريق براي هر سه گروه 9 تا 18 حاملگي بود. در روز 18 جنينها از رحم مادر خارج شده پس از اندازه‌گيري قد و وزن؛ جنينها از نظر وجود ناهنجاريها (ناهنجاري‌هاي ستون مهره‌ها؛ ناهنجاري‌هاي اندام و ناهنجاري‌هاي جمجمه) بررسي شده و مشاهدات ثبت گرديد. ناهنجاري‌هاي موجود در چهار گروه بررسي و به كمك نرم افزارspss مقايسه شدند.

نتايج: نتايج در گروهي كه  mg/kg75-25 دارو دريافت كرده بودند كاهش قد و وزن و افزايش انواع ناهنجاري نسبت به گروه‌هاي كنترل 1 و 2 مشاهده گرديد كه با افزايش دوز و تزريق mg/kg 75 دارو  اين نسبت نيز افزايش يافت. 

نتيجه‌گيري: با توجه به داده‌ها مي‌توان لاموتريژين را به عنوان يك ريسك فاكتور در بروز اين ناهنجاري در جنين موش دانست. عده‌اي از محققين كاهش غلظت سرمي فولات و اسيد آمينه متيونين را در بروز اين ناهنجاريها مؤثر مي‌دانند.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: One of the most important complications of antiepileptic drugs (AEDs) is increased congenital malformations. The risk of malformations in such fetuses is 7-10% compared to 2-4% in the general population. Lamotrigine is a recently introduced AED, with fewer teratogenic effects than that of the older ones and without reported teratogenic effects in most cases. Recently some malformations have been reported related to Lamotrigine use in human beings but the reports are scanty and contradictory and no particular patterns of malformations have been presented. This study has been done to detect the teratogenic effects of this drug in mouse fetus.

Materials &amp; Methods: In this study, NRMI mice were divided into four groups: I) control group 1, II) control group 2, with intraperitoneal administration of ethanol solution, III) case group 1, with intraperitoneal administration of three 25 mg/kg doses of Lamotrigine and IV) case group 2, with intraperitoneal administration of three 75 mg/kg doses  of Lamotrigine. Injections were made during the 9th to the 18th days of gestation. On the 18th day of gestation, the fetuses were harvested. The body weight and height were measured and malformations in vertebral column, limbs and cranium were looked for and recorded. Malformations were compared in the four groups by SPSS software. 

Results: In the groups with 25 &amp; 75 mg/kg Lamotrigine administrations, reduction of body weight and height and increased malformations of vertebral column and limbs were noticeable in a dose dependent fashion compared to the control groups number 1 &amp; 2_ cranial malformations were insignificant.

Conclusion: Based on the results, Lamotrigine can be considered as a risk factor for the increase of malformations in the treated animals. As a number of researchers believe that decrease of serum folate and methionine are effective in the appearance of malformations and they may implicate the situation, further studies on the mechanisms of Lamotrigine from this point of view are recom-mended.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>45</FPAGE>
            <TPAGE>53</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Forouzan</Name>
<MidName>F</MidName>
<Family>Rahmani</Family>
<NameE>فروزان</NameE>
<MidNameE></MidNameE>
<FamilyE>رحمانی</FamilyE>
<Organizations>
<Organization>Department of Anatomy, Faculty of Medicine, Shahr-e-Kord University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Department of Anatomy, Faculty of Medicine, Shahr-e-Kord University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>frajaei@qums.ac.ir</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Masoumeh</Name>
<MidName>M</MidName>
<Family>Delaram</Family>
<NameE>معصومه </NameE>
<MidNameE></MidNameE>
<FamilyE>دل‌آرام </FamilyE>
<Organizations>
<Organization>Department of Midwifery, Faculty of Nursing &amp;amp; Midwifery, Shahrekord University of Medical Science &amp;amp; Health Services</Organization>
</Organizations>
<Universities>
<University>Department of Midwifery, Faculty of Nursing &amp; Midwifery, Shahrekord University of Medical Science &amp; Health Services</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Nasrin</Name>
<MidName>N</MidName>
<Family>Forouzandeh</Family>
<NameE>نسرین </NameE>
<MidNameE></MidNameE>
<FamilyE>فروزنده</FamilyE>
<Organizations>
<Organization>Department of Psychological Nursing, Faculty of Nursing &amp;amp; Midwifery, Shahrekord University of Medical Science &amp;amp; Health Services</Organization>
</Organizations>
<Universities>
<University>Department of Psychological Nursing, Faculty of Nursing &amp; Midwifery, Shahrekord University of Medical Science &amp; Health Services</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Lamotrigine</KeyText></KEYWORD><KEYWORD><KeyText>Mouse</KeyText></KEYWORD><KEYWORD><KeyText>Fetus</KeyText></KEYWORD><KEYWORD><KeyText>Teratogenic</KeyText></KEYWORD><KEYWORD><KeyText>Epilepsy</KeyText></KEYWORD><KEYWORD><KeyText>Pregnancy</KeyText></KEYWORD><KEYWORD><KeyText>Anticoagulant drugs</KeyText></KEYWORD><KEYWORD><KeyText>Folic acid</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>223.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>بهادری مسلم، شکور عباس. نقایص زمان تولد. رویان شناسی پزشکی لانگمن. تجدید نظر هشتم. انتشارات چهر،1380، صفحات: 128-127.##Bastaki S.A.M., Padmanabhan R., Abdulrazzaq Y.M., Chandranth S.I., Shafiulla M. Studies on the terato-genic effect of lamotrigine in mouse fetuse. Frontier in fetal health (a Global perspective). Volume 3, Number 11/12, 2001,295 2001;3(11-12):295.##Beghi E., Annegers J.F., Pergnancy registries in epilep-sy. Epilepsia.2001;42(11):1422-5.##Mark S., Yerby M.S., Kaplan P., Tran T. Risks and management of pregnancy in women with epilepsy. Cleveland clinic Journal of Medicine.2004;71(2suppl): 25-37.##Richens A. Safety of Lamotrigine. Epilepsia.1994;35 (Suppl 5):37-40.##Curry W.J., Kulllling D.L. Newer Anticonvulsant drugs; gabapentin, lamotrigine, febamate, tiagbin, fos-phentyoin. Am Fam Physician.1998;57:513-520.##Young L.T., Robb J.C., Patelis- Siotis I., et al. Acute treatment of bipolar depression with gabapentine. Biol Psychiatery.1997;42:851-53.##Kusumakar V., Yathman Ln. Lamotrigine Treatment of rapid cycling bipolar disorder. Am J Psychiatery.1997; 154:1171-2.##Mather G.G., Levy R.H. Anticonvulsant. Levy R.H., Thummel K.E., Tager W.F., Hanster P.D., Eichelbaum M. Metabolic Drug interactions, Philadelphia:Lippicott Williams &amp; Wilkiins Company Kluwer.2000;218-219.##James O., Mc Nammara. Druge effective in the thera-py of the epilepsia. Hardman J., Limbird Lee E., Good-man &amp; Gillmans the pharmacological basis of thera-peutic. 10th Edition Mc Grow hill Company.2001;539-540.##Ohman I., Vitols S., Tomson T. Lamotrigine in preg-nancy: pharmacokinetics during delivery, in the neo-nate, and during lactation.Epilepsia.2000;41(6):709-13.##Rambeck B., Kurlemann G., Stodieck S.R., May T. W., Jurgens U. Concentrations of Lamotrigine in a mother on lamotrigine treatment and her new born child. Eur J Clin pharmacol.1997;51(6):481-4.##Tomson T., Ohman I., Vitols S. Lamotrigine in preg-nancy and Latction: a case report. Epilepsia.1997;38 (9):1039-40.##Leppik I.E., Antiepileptic drugs in development: pros-pects for the near future. Epilepsia.1994;35(suppl 4): 29-40.##Iqbal M.M., Ryan W.G., Effect of antimanic mood-stabilizing drugs on fetuses, Neonates,and Nursing Infants. Sourthern Medical journal.2001;94(3):304-22.##Loiuseau P., New medical treatment of epilepsy. Presse- Med.1996;23;25(10):481-3.##Marchi N.S., Azouble R., Tognola W.A. Teratogenice effects of lomotrigine on rat fetal brain: amorpho-metrice study. Arq Neuropsiquiatr.2001;59(2-B):362-4.##Morrell M.J. The new antiepileptic drugs and woman: efficacy, reproductive health, pregnancy and fetal out-come. Epilepsia.1996;37(suppl 6):34-44.##Cunnigton M., Tennis P. Lamotrigine and a risk of malformation in pregnancy. Neurology online.2005;64: 955-960.##Fazio A., Artesi C., Russo M., Trio R., Oterio G., Pisani F. A liquid chromatographic assay using a high-speed colmn for the determination of lamotrigine a new antiepileptic drugin human plasma. Ther Drug Monti. 1992;14(6): 509-12##Devinsky O., Vazquez B., Luciano D. New antiepi-leptic drugs for children: felbamate, gabapentin, lamot-rigine, and vigabatrin : J Child Neural.1994;9(Suppl 1 S):33-45.##Canavero S., Bonicalzi V. Drug therapy of trigeminal neuralgia.2006;6(3):429-40.##Lampl C., Katsarava Z., Diener H.C., Limmroth V. Lamotrigine reduces migraine aura and migraine attacks in patients with migraine with aura. J Neurol Neurosurg Psychiatry.2005;76(12):1730-2.##Nahlik L. Lamotrigine (lamictal) when monoteraphy just isn’t enough. The university of Chicago Hospital. 1996;l37:5-6.##Haddad J., Messer J. Feta lalcohol syndrom. Report of three siblings. Neuropediatrics.1994;25:109-11.##Jacobson J.L., Jacobson S.W. Sokol R.J. Mmmartier S.S., at al. Teratogenice effect of alcohol on infant development. Alcohol Clin Exp Res.1993;17:174-83.##Gage J.J.C., Sulik K.K. Pathogenesis of athanol-induced hydronrphrosis and hydroureter as demonst-rated following in vivo expousre of mouse embryo. Teratology.1991;44:299-312.##Maurceri H.J., Lee W.H., Coneay S. Effects of etha-nol on insuline-like growth factor-II relase from fetal organssss. Alcohol Clin Exp Res.1994;18:35-41.##Padmanabhan R., Abdulrazzaq Y.M., Bastaki S.M.,  Shafiulla M., Chandra S.I. Experimental studies on reproductive toxicologic effects of lamotrigine in mice. Birth Defects Res Part B Dev Repord Toxicol.2003;68 (5):428-38.##Nau H. Pharmacokinetices of valproic acid and its metabolites in pregnant patient. In: Janz D (ed). Epi-lepsy, pregnancy and the child: from Raven press. New York: USA,131-44,1981.##Nulman I., Laslo D., Koren G. Treatment of epilepsy in pregnancy.  Drugs.1999;57:535-544.##Minns R.A. Folic acid and neural tube defects. Spinl cord1998;34:460-465.##Perucca E. Birth defects after prenatal exposure to antiepileptic drugs. Lancent Neural.2005 ;4(11):781-6##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>بررسی مقایسه‌ای تستهای FSH سرم و pH واژن در تشخیص یائسگی  </TitleF>
    <TitleE>The comparison of serum Follicle-Stimulating Hormone (FSH) and vaginal pH for the diagnosis of menopause</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: با وجود پیشرفت‌هایی که برای اندازه‌گیری هورمون محرکه فولیکولی (FSH) حاصل شده به بررسی pH واژن کمتر توجه شده است. تاكنون اندازه‌گيري FSH به عنوان تست تشخیص يائسگي مطرح بوده است. بررسي‌هاي انجام شده نشان مي‌دهد استفاده از pH واژن مي‌تواند به تشخيص يائسگي كمك نمايد كه روشي آسان، غيرتهاجمي و ارزان است. هدف از انجام اين پژوهش مقايسه‌اي بين ميزان FSH سرم و pH ترشحات واژن در تشخيص يائسگي است.
روش بررسي: مطالعه حاضر مطالعه‌اي توصيفي- مقطعي است كه روي 120 بيمار با علائم باليني يائسگي در محدودة سني 95-31 سال، مراجعه كننده به درمانگاه يائسگي بيمارستان قائم (عج) از دي ماه 83 تا تير ماه 84 انجام شده است. روش نمونه‌گيري غيرتصادفی و مبتني بر هدف بود. جمع‌آوري اطلاعات به وسيله پرسشنامه انجام گرديد و دو متغير كمي pH واژينال با استفاده از pH سنج مخصوص و FSH سرم در آزمايشگاهي معين براي تمامي بيماران اندازه‌گيري و علاوه بر آن علائم بالینی بیماران ثبت شد. داده‌ها در برنامة آماري SPSS تجزيه و تحليل شدند و نتايج با آزمون 2 و محاسبه ضريب توافق  Kappa مورد ارزيابي قرار گرفت. 05/0 p از نظر آماری معنی‌دار تلقی شد.
نتايج: براساس اطلاعات حاصل از مطالعه حاضر ميزان متوسط pH واژن و در غياب عفونت‌هاي واژينال، در زنان يائسه مورد مطالعه 53/033/5 بود (با حداقل 1/4 و حداکثر 5). با در نظرگرفتن نقطه برش 5/4 برای pH واژن و تست مبنای FSH mIU/ml20FSH&gt; که معیار و شاخص یائسگی است( ميزان حساسيت pH در تشخيص يائسگي 97% تعيين گرديد. میانگین و انحراف معیار میزان هورمون FSH در زنان تحت مطالعه mIU/ml 42/679/80 است.
نتيجه‌گيري: اندازه گيري pH واژن در تشخيص يائسگي حساسيتي شبيه اندازه‌گيري ميزان FSH سرم دارد و می‌تواند جایگزین مناسبی درمقابل FSH سرم باشد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Because of improvements in the measurement methods of FSH levels in serum, there is less interest in evaluating vaginal pH for the diagnosis of menopause nowadays. The traditional test to diagnose menopause has been FSH, so far. In recent studies it has been shown that diagnosis of menopause by testing for vaginal pH is a simple, non-invasive and inexpensive method .This study intended to compare diagnostic value of vaginal pH and serum FSH in the diagnosis of menopause. 
Materials &amp; Methods: This article is a descriptive cross-sectional study taking place from June to July 2005. 120 menopausal women, aged 31 to 95 years that were being referred to a meno-pausal clinic in Qaem Hospital during the study, were chosen by a target-based nonrandom sampling technique for the study. A questionnaire was used for collecting data from the patients. In addition, pH test strips were used for vaginal pH measurements and the patients&#39; serum FSH were evaluated in a definite laboratory and their clinical signs and symptoms were recorded. The data was analyzed by SPSS software and the statistical significant of the results were tested by 2 in comparison with the kappa coefficient of agreement. P0.05 was consi-dered as the significance level of the study.
Results: According to the gathered data in the study, the average vaginal pH in the patients, in the absence of vaginal infections, was 5.330.53 (with a minimum of 4.1 and a maximum of 5) With attention to the cut of point of 4.5 for vaginal pH and the baseline FSH &gt;20 mIU/ml that characterizes menopause, the sensitivity of pH-meter in diagnosing menopause was determined to be 97%. The mean average and the standard deviation of FSH levels in this study was 80.79 6.42.
Conclusion: Vaginal pH sensitivity in the diagnosis of menopause is similar to serum FSH and could be used as a suitable alternative.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>53</FPAGE>
            <TPAGE>59</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Sedigheh</Name>
<MidName></MidName>
<Family>Ayaty</Family>
<NameE>صدیقه</NameE>
<MidNameE></MidNameE>
<FamilyE>آیتی</FamilyE>
<Organizations>
<Organization>Department of Obstet . and Gynecol .Faculty of Medicine, Mashhad Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Department of Obstet . and Gynecol .Faculty of Medicine, Mashhad Medical Sciences University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>sed-ayati@yahoo.com</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Zohreh</Name>
<MidName>Z</MidName>
<Family>Yousefi</Family>
<NameE>زهره</NameE>
<MidNameE></MidNameE>
<FamilyE>یوسفی</FamilyE>
<Organizations>
<Organization>Department of Obstet . and Gynecol .Faculty of Medicine, Mashhad Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Department of Obstet . and Gynecol .Faculty of Medicine, Mashhad Medical Sciences University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mohammad Taghi</Name>
<MidName>MT</MidName>
<Family>Shakeri</Family>
<NameE>محمدتقی</NameE>
<MidNameE></MidNameE>
<FamilyE>شاکری</FamilyE>
<Organizations>
<Organization>Department of Community Medicine &amp;amp; Public Health, Faculty of Medicine, Mashad University of Medical Sciences</Organization>
</Organizations>
<Universities>
<University>Department of Community Medicine &amp; Public Health, Faculty of Medicine, Mashad University of Medical Sciences</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Menopause</KeyText></KEYWORD><KEYWORD><KeyText>Follicle stimulating hormone</KeyText></KEYWORD><KEYWORD><KeyText>Vaginal pH</KeyText></KEYWORD><KEYWORD><KeyText>Diagnosis</KeyText></KEYWORD><KEYWORD><KeyText>Sensitivity</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>224.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Cedars M.I., Euans M., Scott J.R., Gibbs R.S., KarLan B.Y., Haney A.F. Danforth’s obstetrics and gynecolo-gy. 9th. Philadelphia: Lippincott Williams and Wilkins. 2003;pp:721-739.##Speroff L., Frits M.A. Clinical Gynecologic Endocrino-logy and in fertility .7th Edition. Philadelphia:lippincott Williams &amp; wilkins publishers.2005;pp:621-640.##Mohammad K., Sadat Hashemi S.M., Farahani F.K. Age at natural menopause in Iran. Maturitas.2004;49 (4):321-6.##semmens J.P., Wagner G. Estrogen deprivation and vaginal function in postmenopausal women. JAMA 1982;248:445-8.##Ouslander J.G., Cooper E.B.S., Godley D. Estrogen treatment for incontinence in frail older women. J Am Geriatr Soc.1999;47:1383-4.##Cruickshank R., Sharman A. The biology of the vagina in human subjects: I glycogen in the vaginal epithelium and its relation to ovarian activity , II , the bacterial sura and secretion of the vagina at various age periods and their relation to glycogen in the vaginal epithelium, III, vaginal discharge of non-infective origin. J Obstet Gynecol Br Empire.1934;41:190-226.##Roz R., staumm W.E. A controlled trial of intr avaginal estriol in postmenopausal women with recurrent urinary tract infections. N Engl Med.1993;329:753-6.##Rein M.F., Multer M. Trichomonas vaginalis and trichomoniasis. In: Holmes KK. Mard P-A, Sparling PF, Wiesner PJ, Cates Jr, W, Lemon SM, et al. Sexual-ly transmitted diseases. 2nd ed. New York: McGraw- Hill;1990.pp:481-92.##Boskey E.R., Telsch K.M., Whaley K.J., Moench T.R., Cone R.A. Acid production by vaginal flora in vitro is consistent with the rate and extent of vaginal acidifica-tion. Infect Immun.1999;67(10):5170-5.##Lang W. Vaginal acidity and PH: a review. Obstet Gynecol Surv.1955;10:546-60.##Rakoff A.E., Feo L.G., Goldstein L. The biological characteristics of the normal vagina. Am J Obstet Gynecol.1944;47:467-94.##Elia G., Bergman A. Estrogen effects on the urethra: beneficial effects in women with genuine stress incon-tinence. Obstet Gynecol Surv.1993;48(7):509-17.##Caillouette J.C., Sharp C.F., Zimmerman G.J., Ros S. Vaginal PH as a marker for bacterial pathogens and menopausal status. Am J Obstet Gynecol.1997;176(6): 1275-7.##Milsom I., Arvidsson L., Ekelund P., Molander U., Eriksson O. Factors influencing vaginal cytology, PH and bacterial flora in elderly women. Acta Obstet Gynecol Scand.1993;72(4):286-91.##Pandit L., Ouslander J.G. Postmenopausal vaginal atrophy and atrophic vaginitis. Am J Med Sci.1997; 314(4):228-31.##Roy S., Caillouette J.C., Roy T., Faden S. Vaginal PH is similar to follicle-stimulating hormone for meno-pause diagnosis. Am J Obstet Gynecol.2004;190(5): 1272-7.##Melis G.B., Ibba M.T., Steri B., Kotsonis P., Matta V., Paoletti A.M. Role of pH as a regulator of Vaginal physiological environment. Minerva Ginecol.2000;52 (4):111-21.##Garcia-Closas M., Herrero R., Bratti C., Hilde sheim A., Sherman M.E., Morera L.A., Sehiffman M. Epide-miologic determinats of vaginal PH. Am J Obstet Gynecol.1999;180(5):1060-6.##Samsioe G. Urogenital aging: a hidden Problem. Am J Obstet Gynecol.1998;178(5):S 245-9.##Notelovitz M. Estrogen therapy in the management of problems associated with urogenital ageing; a simple diagnostic test and the effect of the route of hormone administration. Maturitas.1995;22(suppls):31-3.##Roy S., Caillouette J.C., Faden J.S., Roy T., Ramos D.E., Improving appropriate use of antifungal medica-tions: the role of an over-the counter vaginal PH self- test device. Infect Dis Obstet Gynecol.2003;11(4):209-16.##Casper F., Petri E., Vaginal ring study group. Local treatment of urogenital atrophy with an estradiol-releasing vaginal ring a comparative and a placebo-controlled multicenter study. Vaginal Ring study Group. Int Urogynecol. J Pelvic Floor Dyshunct.1999; 10(3):171-6.##Nilsson K., Risberg B., Heimer G. The vaginal epithelium in the postmenopause- cytology, histology and PH as methods of assessment. Maturitas.1995;21 (1):51-6.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>شيوع گرفتگي عضلاني در دوران بارداري و اثر مكمل درماني بر آن</TitleF>
    <TitleE>Prevalence of leg cramps during pregnancy and effects of supplemental therapy</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: گرفتگی عضلانی، انقباض دردناک عضلات است که به طور شایع در دوران بارداري به خصوص در اندام تحتانی دیده می‌شود. در ايران درمان خاصي برای این اختلال، متداول نمي‌باشد؛ لذا با هدف دستیابی به راه حل مناسب با امکانات داخل کشور مطالعه حاضر طراحی شد.  
روش بررسي: از ميان 401 زن باردار مراجعه‌كننده (در نيمه دوم بارداري) به درمانگاه پره‌ناتال بيمارستان امام خميني (ره) تهران در سال 83-1382، 217 نفر (5/54%) كه از گرفتگي دردناك عضلات ساق پا (با شدت و تناوب متفاوت) شكايت داشتند مورد بررسي قرار گرفتند. تعدادي از اين بيماران كه پس از بررسي‌هاي پاراكلينيك، هيچگونه اختلال الكتروليتي نداشتند و همچنين متعاقب ارزيابي تغذيه‌اي ريزمغذيها را در رژيم غذايي در حد استاندارد و توصيه شده دريافت كرده بودند، وارد فاز دوم مطالعه شدند. در اين مرحله بيماران به دسته‌هاي مكمل درماني به مدت 2 هفته (كلسيم، منيزيوم، ويتامين‌هاي گروه B) و گروه شاهد تقسيم شدند. سپس براساس معيار بهبودي كامل (برطرف شدن كامل علائم از نظر شدت و تناوب) با يكديگر مقايسه شدند. داده‌ها پس از جمع‌آوري در نرم افزار آماريSPSS  ذخيره شده و فرضيه‌هاي طرح از طريق آزمون‌هاي آماري 2، t و مدل رگرسيون لجستيك بررسي شدند. 
نتایج: رابطه آماری معنی‌داری بین بهبودی کامل با مکمل‌ درمانی ویتامین B در مقايسه با گروه كنترل مشاهده شد. 
به طوريكه بهبودي كامل 71% در گروه دريافت كننده مكمل ويتامين‌هاي گروه B در مقابل 9% در گروه كنترل، 29% در گروه منيزيوم و 52% در گروه كلسيم (0001/0p&lt;) برآورد شد. 
نتیجه گیری: شیوع بالای گرفتگی عضلانی به خصوص در اندام تحتانی در میان زنان باردار ایرانی (54%)، با رژیم غذایی و عادات زندگی ارتباط خاصی ندارد؛ اما مکمل درمانی ریزمغذیها (اضافه بر تغذيه عادي روزانه) مي‌تواند تأثیر به سزایی در درمان اين مشكل داشته باشد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Leg cramps are common painful spasms especially in the lower extremities during pregnancy. The purpose of this study was to find a suitable alternative in the treatment of the disease. 
Materials &amp; Methods: 217 patients reported leg cramps with different degrees and frequencies among 401 pregnant women in the second half of their pregnancies who visited the Prenatal Clinic of Imam Khomeini Hospital from July to December 2002. After preliminary evaluations for ruling out electrolyte imbalances or insufficient supply of dietary micronutrients, patients were randomly allocated into supplemental therapy (Calcium, magnesium or vitamin B intake for 2 weeks) and control groups. The groups were compared after 4 weeks according to their complete relief from leg cramps. The clinical findings and the data collected from the patients were analyzed by chi-square and t-student tests and a logistic regression model using the SPSS (V.10) software.  
Results: There was a significant improvement in patients receiving vitamin B with 71% complete and 19% relative relief from leg cramps, compared to 9% complete relief in the control group- 29% and 52% in the groups receiving magnesium and calcium respectively (p&lt;0.0001).
Conclusion: Although the high prevalence of leg cramps (55%) in the patients was not necessary-ly related to dietary habits, but it seemed that supplementing symptomatic patients with vitamin B could be beneficial.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>59</FPAGE>
            <TPAGE>65</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Farnaz</Name>
<MidName>F</MidName>
<Family>Sohrabvand</Family>
<NameE>فرناز</NameE>
<MidNameE></MidNameE>
<FamilyE>سهراب‌وند</FamilyE>
<Organizations>
<Organization>Vali-e- Asar Reproductive Health Research Center,Tehran Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Vali-e- Asar Reproductive Health Research Center,Tehran Medical Sciences University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>fsohrabvand@yahoo.com</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Mamak</Name>
<MidName>M</MidName>
<Family>Shariat</Family>
<NameE>مامک</NameE>
<MidNameE></MidNameE>
<FamilyE>شریعت</FamilyE>
<Organizations>
<Organization>Vali-e- Asar Reproductive Health Research Center,Tehran Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Vali-e- Asar Reproductive Health Research Center,Tehran Medical Sciences University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Fedyeh</Name>
<MidName>F</MidName>
<Family>Haghollahi</Family>
<NameE>فدیه</NameE>
<MidNameE></MidNameE>
<FamilyE>حق‌اللهی</FamilyE>
<Organizations>
<Organization>Vali-e- Asar Reproductive Health Research Center,Tehran Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Vali-e- Asar Reproductive Health Research Center,Tehran Medical Sciences University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Soghra</Name>
<MidName>S</MidName>
<Family>Khezerdoust</Family>
<NameE>صغری</NameE>
<MidNameE></MidNameE>
<FamilyE>خظردوست</FamilyE>
<Organizations>
<Organization>Vali-e- Asar Reproductive Health Research Center,Tehran Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Vali-e- Asar Reproductive Health Research Center,Tehran Medical Sciences University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Abbas</Name>
<MidName>A</MidName>
<Family>Rahimi Foroushani</Family>
<NameE>عباس</NameE>
<MidNameE></MidNameE>
<FamilyE>رحیمی فروشانی</FamilyE>
<Organizations>
<Organization>Epidemiology Department, Faculty of Publi Health, Tehran Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Epidemiology Department, Faculty of Publi Health, Tehran Medical Sciences University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Leili</Name>
<MidName>L</MidName>
<Family>Nazemi</Family>
<NameE>لیلی</NameE>
<MidNameE></MidNameE>
<FamilyE>ناظمی</FamilyE>
<Organizations>
<Organization>Human Nutrition and Biochemistry Department, Faculty of Public Health, Tehran Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Human Nutrition and Biochemistry Department, Faculty of Public Health, Tehran Medical Sciences University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Maryam</Name>
<MidName>M</MidName>
<Family>Chammari</Family>
<NameE>مریم</NameE>
<MidNameE></MidNameE>
<FamilyE>چمری</FamilyE>
<Organizations>
<Organization>Human Nutrition and Biochemistry Department, Faculty of Public Health, Tehran Medical Sciences University</Organization>
</Organizations>
<Universities>
<University>Human Nutrition and Biochemistry Department, Faculty of Public Health, Tehran Medical Sciences University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Leg cramps</KeyText></KEYWORD><KEYWORD><KeyText>Vitamin B1</KeyText></KEYWORD><KEYWORD><KeyText>Vitamin B6</KeyText></KEYWORD><KEYWORD><KeyText>Pregnancy</KeyText></KEYWORD><KEYWORD><KeyText>Calcium</KeyText></KEYWORD><KEYWORD><KeyText>Magnesium</KeyText></KEYWORD><KEYWORD><KeyText>Supplemental therapy</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>225.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Schwellnus M.P. Skeletal muscle cramps during exer- cise: The physician &amp; Sport medicine.1999;27:12-13.##Duke J.A. Total health for women: Muscle cramp. 2000;Rodale book.##Herbal remedies, USA site. Muscle cramps, muscle spasm, leg cramps, feet cramps.2001.##Valbo A., Bohmer T. Leg cramps in pregnancy How common are they? Tidsskr Nor laegeform.1999;119 (11):1589-90.##Gary F. Cunningham F.C. Medical &amp; surgical compli-cations in pregnancy. Williams Obstetrics.21st Edition, Mc Graw hill.2001;p:1141.##Cunningham F.C. Renal &amp; Urinary Tract disorders: Williams Obstetrics. 21st Edition, MC Graw Hill.2001; p:1251.##Young G.L., Jewell D. Interventions for leg cramps in pregnancy. Cochrane Database Syst Nov.2002;(2):CD 000121.##Avsar A.F., Ozmen S., Soylemez F. Vit ?1 &amp; B6 substitution in pregnancy for leg cramps. Am J Obsted Gynecol.1996;125(1):233-4.##Dahle L.O., Berg G., Hammar M., Hurtig M., Larsson L., et al. The effect of oral Magnesium substation on pregnancy, Induced leg cramps. Am J Obstet Gynecol. 1995;173 (1):175-180.##Young G.C., Jewell D. Intervention for leg cramps in pregnancy. Cochrane Database Syst Rev.2000;(2): CD 000121.##Hammer M., Larsson L. Calcium treatment of leg cramps in pregnancy effect on clinical symptoms and total serum and ionized serum calcium concentration.  Acta Obstet Gynecol Scand.1981;60(4):345-7.##Frussor A., Zarate M., Augustovki M. Magnesium for the treatment of nocturnal leg cramps: a cross over randomized trial. J Fam Pract.1999;48(11):868-71.##Surgery B.C., Sowerbery T. Interventions for leg cramps in pregnancy. Cochrane Data Base Syst Rev. 2002;(1):CD000121.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

<ARTICLE>
    <TitleF>دلايل ختم بارداري در سه ماهه سوم در مركز آموزشي‌ـ درماني هاجر شهركرد در سال 1383</TitleF>
    <TitleE>The reasons for the termination of pregnancies in the third trimester in Shahr-e-kord’s Hadjar hospital during 2005</TitleE>
    <TitleLang_ID>2</TitleLang_ID>
    <ABSTRACTS>
        <ABSTRACT>
            <Language_ID>1</Language_ID>
            <CONTENT>زمينه و هدف: امروزه مشاهده مي‌شود بيشتر مادران مراجعه كننده به بيمارستان جهت ختم بارداري در سه ماهه سوم، در فاز زايماني قرار ندارند و بدون شروع انقباضات رحمي بستري مي‌شوند و بارداري آنها ختم مي‌گردد. با توجه به اهميت سلامت مادران و نوزادان و نقش سزارين‌هاي غيرضروري، پژوهش حاضر به منظور تعيين دلايل ختم بارداري در سه ماهه سوم در مركز آموزشي‌‌‌ـ درماني هاجر شهركرد انجام شده است. 
روش بررسي: در اين مطالعه توصيفي‌ـ تحليلي تعداد 750 نفر از زناني كه جهت ختم بارداري در سه ماهه سوم در بخش زايمان مركز آموزشي‌ـ درماني هاجر شهركرد طي ارديبهشت تا آذر 1383 بستري شده بودند، به روش تصادفي و در سه شيفت صبح، عصر و شب انتخاب شده و مورد بررسي قرار گرفتند. ابزار گردآوري اطلاعات در اين پژوهش، فرم ثبت اطلاعات و چك ليست بود. از معاينه واژينال بيمار، مطالعه پرونده، مصاحبه با مادر و معاينه فيزيكي نوزاد براي تكميل فرم ثبت اطلاعات و چك ليست استفاده شد. اطلاعات حاصل با استفاده از نرم افزار SPSS و آزمون‌هاي آماري T و 2 مورد تجزيه و تحليل قرار گرفت و 05/0p&lt; به عنوان سطح معني‌داري در نظر گرفته شد.
نتايج: براساس نتايج حاصل از پژوهش 298 نفر (7/39%) از واحدهاي پژوهش به علت شروع دردهاي زايماني و 452 نفر (3/60%) بدون درد زايمان و به توصيه پزشك و ساير مراقبين بهداشتي‌ـ درماني، جهت ختم بارداري مراجعه كرده بودند. در گروه اخير در 2/23% افراد، مواردي مثل سزارين قبلي، تمايل به سزارين، كاهش حركات جنين، بارداري ديررس، فشار خون بالا در مادر، جفت سرراهي، جدا شدن زودرس جفت و كاهش حجم مايع آمنيوتيك به عنوان علت اقدام به سزارين مطرح بود. ميانگين امتياز بيشاپ سرويكس در گروهي كه به علت شروع درد زايمان مورد ختم بارداري قرار گرفته بودند، بيشتر از گروهي بود كه بدون درد زايمان و به توصيه پزشك و ساير فراهم كنندگان مراقبت بستري و مورد ختم بارداري قرار گرفته بودند (001/0p&lt;، 541=df، 45/40=t). ارتباط امتياز بيشاپ سرويكس با نوع زايمان معني‌دار بود و در افرادي كه اين امتياز كمتر از 5 بود، عمل سزارين بيشتر انجام شده بود(001/0p&lt;، 1=df، 9/113=2). رابطه بين علت ختم بارداري و نوع زايمان پس از حذف موارد سزارين تكراري و تمايل به سزارين معني‌‌دار بود و افرادي كه بدون شروع درد زايمان بستري شده بودند، بيشتر تحت عمل سزارين قرار گرفته بودند (001/0p&lt;، 1=df، 26/64=2). سن بارداري براساس تاريخ اولين روز قاعدگي بيمار (LMP) و سونوگرافي در اين گروه بيشتر از گروهي بود كه به علت شروع دردهاي زايماني مورد ختم بارداري قرار گرفته بودند(001/0p&lt;، 311=df، 70/3=t). تفاوت معني‌داري در وزن نوزادان در دو گروه وجود نداشت.
نتيجه‌گيري: گرفتن شرح حال دقيق در مراقبت‌هاي دوران بارداري جهت تعيين سن بارداري، انجام سونوگرافي در 26 هفته اول بارداري و آموزش به تمامي خانم‌هاي باردار در مورد زمان مراجعه به بيمارستان جهت ختم بارداري و عوارض ناشي از بستري شدن زودرس، تشکيل کميته‌های تخصصی تصميم‌گيري در مورد ختم بارداری در بيمارستانها و تدوين آئين‌نامه‌هاي خاص در اين مورد، از اقداماتي است كه مي‌توان در جهت جلوگيري از ختم زودرس بارداري انجام داد.</CONTENT>
        </ABSTRACT>
        <ABSTRACT>
            <Language_ID>2</Language_ID>
            <CONTENT>Introduction: Observations show that the majority of pregnant women hospitalized in the third trimester of pregnancy, their pregnancies are terminated in the absence of any labor pain. Because of the importance of mother and baby  health, this study was designed to assess the reasons for these terminations  in Hadjar’s University  Hospital in Shahr-e-Kord. 
Materials &amp; Methods: In this descriptive and analytical  study, 750  women who were hospi-talized for the termination of pregnancy, were selected randomly and assessed  in morning, evening and night shifts. A questionnaire and a check list were used for data collection. Hospital records, interviews with mothers, a vaginal exam and physical exam of infants were used to complete the form and the check list. Data were analized by SPSS software and t, Chi square tests were used and p&lt;0.05 was considered significant. 
Results: Based on the results, 298 (39.7%) of pregnancies  were terminated for labor pain and 452 (60.3%) were terminated according to physicians’ advice or other health care providers’ without presence of labor pain. In the latter group, 23.2% of pregnancies were terminated for a history of previous cesarean section, elective cesarean sections, reduction of fetal movements, post-term pregnancies, maternal hypertention, placenta previa, placenta abruption or oligohydro-amnious.The mean Bishop score for induction was greater in women whose pregnancies were terminated for labor pain than those terminated according to physicians’ or  any other health care providers’ advice (df=541, p&lt;0.001). The correlation between Bishop score and mode of delivery was significant  and in women whose Bishop score was less than 5, cesarean section was higher (df=20, p&lt;0.001). After the elimination of previous and elective cesarean sections, the correlation between the causes of terminations and mode of delivery was significant and  most hospitalized women terminated their pregnancieis, by cesarean section without  presence of labor pain (df=16, p&lt;0.001), although in this group the mean gestational age based on LMP and sonography was greater than those with labor pain (t= 3.7, df= 311, p&lt;0.001). There were no significant differences in the weight of infants in the two groups. 

Conclusion: Taking  the exact information in prenatal cares about the gestational age, carrying out a sonography  in the first 26 weeks of pregnancy, educating  pregnant women about the time of hospitalization for the termination of pregnancy and complications of early hospitalization, forming a specialty committee to decide on the termination of pregnancies in hospitals and setting practice guidelines  in this regard,are efforts  to prevent early termination of pregnancies.</CONTENT>
        </ABSTRACT>
    </ABSTRACTS>
    <PAGES>
        <PAGE>
            <FPAGE>65</FPAGE>
            <TPAGE>73</TPAGE>
        </PAGE>
    </PAGES>
    <AUTHORS>
        <AUTHOR>
<Name>Masoumeh</Name>
<MidName>M</MidName>
<Family>Delaram</Family>
<NameE>معصومه </NameE>
<MidNameE></MidNameE>
<FamilyE>دل‌آرام </FamilyE>
<Organizations>
<Organization>Department of Midwifery, Faculty of Nursing &amp;amp; Midwifery, Shahrekord University of Medical Science &amp;amp; Health Services</Organization>
</Organizations>
<Universities>
<University>Department of Midwifery, Faculty of Nursing &amp; Midwifery, Shahrekord University of Medical Science &amp; Health Services</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email>mdelaram@skums.ac.ir</Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Forouzan</Name>
<MidName>F</MidName>
<Family>Rahmani</Family>
<NameE>فروزان</NameE>
<MidNameE></MidNameE>
<FamilyE>رحمانی</FamilyE>
<Organizations>
<Organization>Department of  Anatomy, Faculty of Medicine,  Shahr-e-Kord University of Medical Science &amp;amp; Health Services</Organization>
</Organizations>
<Universities>
<University>Department of  Anatomy, Faculty of Medicine,  Shahr-e-Kord University of Medical Science &amp; Health Services</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR><AUTHOR>
<Name>Alireza</Name>
<MidName>A</MidName>
<Family>Ahmadi</Family>
<NameE>علیرضا</NameE>
<MidNameE></MidNameE>
<FamilyE>احمدی</FamilyE>
<Organizations>
<Organization>Department of  Biomedicine women, Research Center,Alzahra University</Organization>
</Organizations>
<Universities>
<University>Department of  Biomedicine women, Research Center,Alzahra University</University>
</Universities>
<Countries>
<Country>Iran</Country>
</Countries>
<EMAILS>
<Email></Email>
</EMAILS>
</AUTHOR>
    </AUTHORS>
    <KEYWORDS>
        <KEYWORD><KeyText>Termination of pregnancy</KeyText></KEYWORD><KEYWORD><KeyText>Third trimester</KeyText></KEYWORD><KEYWORD><KeyText>Cesarean section</KeyText></KEYWORD><KEYWORD><KeyText>Delivery</KeyText></KEYWORD><KEYWORD><KeyText>High risk pregnancy</KeyText></KEYWORD>
    </KEYWORDS>
    <PDFFileName>226.pdf</PDFFileName>
    <REFRENCES>
        <REFRENCE>
            <REF>Savitz D.A., Terry J.W. Jr., Dole N., Thorp J.M. Jr., Siega-Riz A.M., Herring A.H. Comparison of preg-nancy dating by last menstrual period, ultrasound scan-ning, and their combination. Am J Obstet Gynecol. 2002;187(6):1660-6.##Cunningham F.G., Gant N.F., Leveno K.J., Gilstrap L. C., Hauth J.C., Wenstrom K.D.  Ultrasound and dopp-ler. Williams obstetrics. from McGRAW-Hill company Newyork.2001;pp:1111-39.##Johnson D.P., Davis N.R., Brown A.J. Risk of cesa-rean delivery after induction at term in nulliparous women with an unfavorable cervix. Am J Obstet Gynecol.2003;188(6):1565-9.##Bailit J.L., Garrett J.M., Miller W.C., McMahon M.J., Cefalo R.C. Hospital primary cesarean delivery rates and the risk of poor neonatal outcomes. Am J Obstet Gynecol.2002;187(3):721-7.##Jerbi M., Hidar S., Ammar A., Khairi H. Predictive factors of vaginal birth after cesarean delivery. Int J Gynaecol Obstet.2006;94(1):43-4.##Hoffman M.K., Vahratian A., Sciscione A.C., Troen-dle J.F., Zhang J. Comparison of labor progression between induced and noninduced multiparous women. Obstet Gynecol. 2006;107 (5):1029-34.##Heinberg E.M., Wood R.A., Chambers R.B. Elective induction of labor in multiparous women. Does it increase the risk of cesarean section? J Reprod Med. 2002;47(5):399-403.##Seyb S.T., Berka R.J., Socol M.L., Dooley S.L. Risk of cesarean delivery with elective induction of labor at term in nulliparous women. Obstet Gynecol.1999;94 (4):600-7.##Maslow A.S., Sweeny A.L. Elective induction of labor as a risk factor for cesarean delivery among low-risk women at term. Obstet Gynecol.2000;95(6Pt1):917-22.##Dublin S., Lydon-Rochelle M., Kaplan R.C., Watts D.H., Critchlow C.W. Maternal and neonatal outcomes after induction of labor without an identified indica-tion. Am J Obstet Gynecol.2000;183(4):986-94.##Dommergues M., Benachi A., Benifla J.L., des Noettes R., Dumez Y. The reasons for termination of pregnancy in the third trimester. Br J Obstet Gynaecol. 1999;106(4):297-303.##Burrough A. Health problems complicating pregnan-cy. In: Burrough Arlene. Maternity nursing. An Intro-duction Text. 7th Edition. W.B saunders company. 1997;pp:366-372.##Bosma J.M., van der Wal G., Hosman-Benjaminse S. L. Late termination of pregnancy in North Holland. Br J Obstet Gynaecol.1997;104 (4):478-87.##Cunningham F.G., Gant N.F., Leveno K.J., Gilstrap L.C., Hauth J.C., Wenstrom K.D. Obstetrics in Broad Perspective. Williams Obstetrics. From McGRAW-Hill company, Newyork.2001;pp:3-13.##Yeast J.D., Jones A., Poskin M. Induction of labor and the relationship to cesarean delivery: A review of 7001 consecutive inductions. Am J Obstet Gynecol. 1999;180(3 Pt 1):628-33.##Cunningham F.G., Gant N.F., Leveno K.J., Gilstrap L.C., Hauth J.C., Wenstrom K.D. Cesarean Section and Post partum hysterectomy. Williams Obstet. From McGRAW-Hill company, Newyork. 2001;pp:537-563.##Porter M., Bhattacharya S., van Teijlingen E., Templeton A. Reproductive Outcome Following Cae-sarean Section (ROCS) Collaborative Group. Does Caesarean section cause infertility? Hum Reprod.2003; 18(10):1983-6. Review.##شاکریان بهار. بررسی فراوانی نسبی سزارین و علل انجام آن در استان چهار محال و بختیاری. مجله دانشگاه علوم پزشکی شهرکرد، 1383، 6(1). صفحات: 69-63.##Rahnama P., Ziaei S., Faghihzadeh S. Impact of early admission in labor on method of delivery. Int JGynaecol Obstet.2006;92(3):217-20.##Alves B., Sheikh A. Investigating the relationship between affluence and elective caesarean sections. BJOG.2005;112(7):994-6.##Kwee A., Cohlen B.J., Kanhai H.H., Bruinse H.W., Visser G.H. Caesarean section on request: a survey in The Netherlands. Eur J Obstet Gynecol Reprod Biol. 2004;15;113(2):186-90.##Woodrow N.L. Termination review committees: are they necessary? Med J Aust.2003;179(2):92-4.Review.##</REF>
        </REFRENCE>
    </REFRENCES>
</ARTICLE>

    </ARTICLES>
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