<?xml version="1.0" encoding="UTF-8" ?>
<!DOCTYPE Articles SYSTEM "HBI_DTD">


<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>2018</year>
	<month>8</month>
	<day>5</day>
</pubdate>
<volume>19</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>30167393</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>Effect of CatSper and Hv1 Channel Inhibition on Progesterone Stimulated Human Sperm</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: Intracellular calcium and proton concentrations are important factors for activating human sperm. Calcium ion (Ca&lt;sup&gt;2+&lt;/sup&gt;) enters sperm through voltage-dependent calcium channel of sperm (CatSper). Proton was extruded from sperm through voltage-gated proton channel (Hv1). In the present study, the selective inhibitors of the CatSper and Hv1 channels, NNC 55-0396 (NNC) and zinc ion, respectively, were used to investigate functions of these channels.&lt;br /&gt;
Methods: Normal semen samples (n=24) were washed and diluted to 20&amp;times;10&lt;sup&gt;6&lt;/sup&gt; &lt;em&gt;sperm/ml&lt;/em&gt;. The diluted sample was divided into 8 groups, containing Ham&amp;rsquo;s F-10 (the control group), 2 &lt;em&gt;&amp;micro;M&lt;/em&gt; NNC, 1 &lt;em&gt;mM&lt;/em&gt; ZnCl&lt;sub&gt;2&lt;/sub&gt; and NNC+Zn. The other 4 groups were the same as above, except that they contained 1 &lt;em&gt;&amp;micro;M&lt;/em&gt; progesterone. The computer assisted analysis was done by VT-Sperm 3.1 to determine the percentage of motile sperm and sperm velocity. Acrosomal status was monitored by FITC-PSA and viability assessed by Eosin&amp;ndash;Y staining. Statistical comparisons were made using ANOVA followed by Tukey post hoc test. The p&amp;lt;0.05 was considered significant.&lt;br /&gt;
Results: The percentage of viable and motile sperm, curvilinear velocity and other parameters of motility was reduced in all groups containing NNC, zinc and NNC+zinc. Progesterone&amp;ndash;induced acrosome reaction was abolished by each of these inhibitors. The combination effect of NNC plus zinc on motility and progesterone&amp;ndash;induced acrosome reaction was not stronger than NNC by itself.&amp;nbsp;&lt;br /&gt;
Conclusion: CatSper and Hv1 channels play a critical role in human sperm function and viability. It seems that a functional relationship exists between CatSper and Hv1 channels.&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Acrosome reaction, CatSper channel, Hv1 channel, Progesterone, Sperm motility</keyword>
	<start_page>133</start_page>
	<end_page>140</end_page>
	<web_url>https://www.jri.ir/article/10026</web_url>
	<pdf_url>https://www.jri.ir/documents/fullpaper/en/10026.pdf</pdf_url>
	<author_list><author><first_name>Sara</first_name><middle_name></middle_name><last_name>Keshtgar</last_name><suffix></suffix><affiliation>Department of Physiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, 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>keshtgar@sums.ac.ir</email><code>11836</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Hamideh</first_name><middle_name></middle_name><last_name>Ghanbari</last_name><suffix></suffix><affiliation>Endocrinology and Metabolism Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, 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>11837</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Esmaeel</first_name><middle_name></middle_name><last_name>Ghani</last_name><suffix></suffix><affiliation>Endocrinology and Metabolism Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, 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>11838</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Seyed Mostafa</first_name><middle_name></middle_name><last_name>Shid Moosavi</last_name><suffix></suffix><affiliation>Department of Physiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, 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>11839</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

