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<journal>
<language>en</language>
<journal_id_issn>1726-7536</journal_id_issn>
<journal_id_issn_online>1735-8507</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi></journal_id_doi>
<journal_id_isnet></journal_id_isnet>
<journal_id_iranmedex>69</journal_id_iranmedex>
<journal_id_magiran>2139</journal_id_magiran>
<journal_id_sid>288</journal_id_sid>
<pubdate PubStatus="epublish">
	<type>gregorian</type>
	<year>2017</year>
	<month>1</month>
	<day>9</day>
</pubdate>
<volume>18</volume>
<number>1</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>28377895</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Short Term Culture of Vitrified Human Ovarian Cortical Tissue to Assess the Cryopreservation Outcome: Molecular and Morphological Analysis</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt;Background: The aim of the present study was to evaluate the effectiveness of human ovarian vitrification protocol followed with &lt;em&gt;in vitro&lt;/em&gt; culture at the morphological and molecular levels.&lt;br /&gt;
Methods: Ovarian tissues were obtained from 10 normal transsexual women and cut into small pieces and were divided into non-vitrified and vitrified groups and some of the tissues fragments in both groups were randomly cultured for two weeks. The morphological study using hematoxylin and eosin and Masson&amp;#39;s trichrome staining was done. The analysis of mean follicular density, 17-&amp;beta; estradiol (E2) and anti mullerian hormone (AMH), and real-time RT-PCR was down for the evaluation of expression of genes related to folliculogenesis. Data were compared by paired-samples and independent-samples T test. Values of p&amp;lt;0.05 were considered statistically significant.&lt;br /&gt;
Results: The proportion of normal follicles did not show significant difference between vitrified and non-vitrified groups before and after culture but these rates and the mean follicle density significantly decreased in both cultured tissues (p&amp;lt;0.05). The expression of genes was similar in vitrified and non-vitrified groups but in cultured tissues the expression of GDF9 and FSHR genes increased and the expression of FIGLA and KIT-L genes decreased (p&amp;lt;0.05). An increase in E2 and AMH concentration was observed after 14 days of culture in both groups.&lt;br /&gt;
Conclusion: In conclusion, the present study indicated that the follicular development and gene expression in vitrified ovarian tissue was not altered before and after &lt;em&gt;in vitro&lt;/em&gt; culture, thus this method could be useful for fertility preservation; however, additional studies are needed to improve the culture condition.&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>17 beta- Estradiol, Anti- mullerian hormone, Gene expression, Vitrification</keyword>
	<start_page>162</start_page>
	<end_page>172</end_page>
	<web_url>https://www.jri.ir/article/691</web_url>
	<pdf_url>https://www.jri.ir/documents/fullpaper/en/691.pdf</pdf_url>
	<author_list><author><first_name>Mehdi</first_name><middle_name></middle_name><last_name>Ramezani</last_name><suffix></suffix><affiliation>Department of Anatomical Sciences, Medical Sciences Faculty, Tarbiat Modares University, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>1641</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Mojdeh</first_name><middle_name></middle_name><last_name>Salehnia</last_name><suffix></suffix><affiliation>Department of Anatomical Sciences, Medical Sciences Faculty, Tarbiat Modares University, Tehran, Iran</affiliation><first_name_fa>مژده</first_name_fa><middle_name_fa></middle_name_fa><last_name_fa>صالح نيا</last_name_fa><suffix_fa></suffix_fa><email>salehnim@modares.ac.ir, mogdeh@dr.com</email><code>243</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Mina</first_name><middle_name></middle_name><last_name>Jafarabadi</last_name><suffix></suffix><affiliation>Reproductive Health Research Center, Tehran University of Medical Sciences, Tehran, Iran</affiliation><first_name_fa>مينا </first_name_fa><middle_name_fa></middle_name_fa><last_name_fa>جعفرآبادي</last_name_fa><suffix_fa></suffix_fa><email></email><code>754</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

