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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>2016</year>
	<month>6</month>
	<day>12</day>
</pubdate>
<volume>17</volume>
<number>3</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>27478767</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>The Effect of Ammonium Chloride Concentration in In Vitro Maturation  Culture on Ovine Embryo Development</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: Ammonium is produced in culture medium due to amino acids degradation and has adverse effect on &lt;em&gt;in vitro&lt;/em&gt; culture of embryo. In the current study, the purpose was to evaluate the effects of ammuniom chloride (AC) on &lt;em&gt;in vitro&lt;/em&gt; oocyte maturation rate and early embryo development in the sheep and its effect on the expression of Bcl-2.&lt;br /&gt;
Methods: &lt;em&gt;In vitro&lt;/em&gt; maturation (IVM) was performed in the presence of various concentrations (0, 29, 88,132,176&lt;em&gt; &amp;mu;M/ml&lt;/em&gt;) of ammonium chloride (NH4CL) (AC). Meiotic maturation, embryonic development and expression of Bcl2 gene in Blastocyst cells were determined. The data were analyzed by one-way ANOVA and Tukey post HOC test, and values with p&amp;lt;0.05 were considered statistically significant.&lt;br /&gt;
Results: The highest concentration (176 &lt;em&gt;&amp;micro;M&lt;/em&gt;) of AC significantly decreased the rate of fully expanded cumulus cells 24 &lt;em&gt;hr&lt;/em&gt; after IVM compared with the control group (p&amp;lt;0.05). Moreover, significantly lower rates of MII oocytes were found in the 176 &lt;em&gt;&amp;micro;M&lt;/em&gt; AC group compared with the 29 &lt;em&gt;&amp;micro;M&lt;/em&gt; AC group. The percentage of zygotes developing to blastocysts in 176 &lt;em&gt;&amp;micro;M &lt;/em&gt;AC was lower than the other group. Also, supplementation of the oocyte maturation media with 176 &lt;em&gt;&amp;micro;M&lt;/em&gt; AC decreased Bcl2 expression.&lt;br /&gt;
Conclusion: Our results suggested that significant increase in IVM rate could be obtained with supplementation maturation medium with AC in a dose dependent manner. Increased AC concentration led to lower blastocyst rate under normal condition. However, regulation of pro&amp;ndash;apoptotic (Bcl-2) gene did not change with different concentrations of AC supplementing.&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Ammonium chloride, Gene expression, Ovine embryo</keyword>
	<start_page>144</start_page>
	<end_page>151</end_page>
	<web_url>https://www.jri.ir/article/684</web_url>
	<pdf_url>https://www.jri.ir/documents/fullpaper/en/684.pdf</pdf_url>
	<author_list><author><first_name>Ali</first_name><middle_name></middle_name><last_name>Golchin</last_name><suffix></suffix><affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Tabriz, Tabriz, 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>1625</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Reza</first_name><middle_name></middle_name><last_name>Asadpour</last_name><suffix></suffix><affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Tabriz, Tabriz, 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>rasadpour4@gmail.com</email><code>1626</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Leila</first_name><middle_name></middle_name><last_name>Roshangar</last_name><suffix></suffix><affiliation>Department of Anatomical Sciences, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran</affiliation><first_name_fa>ليلا</first_name_fa><middle_name_fa></middle_name_fa><last_name_fa>روشنگر</last_name_fa><suffix_fa></suffix_fa><email></email><code>364</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Raziallah</first_name><middle_name></middle_name><last_name>Jafari-Jozani</last_name><suffix></suffix><affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Tabriz, Tabriz, 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>1627</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

