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    <journal-meta>
      <journal-id journal-id-type="nlm-ta">J Reprod Infert</journal-id>
      <journal-id journal-id-type="publisher-id">arij001</journal-id>
      <journal-title-group>
        <journal-title>Journal of Reproduction &amp; Infertility</journal-title>
      </journal-title-group>
      <issn pub-type="ppub">2228-5482</issn>
      <issn pub-type="epub">2251-676X</issn>
      <publisher>
        <publisher-name>Avicenna Research Institute</publisher-name>
      </publisher>
    </journal-meta>

    <article-meta>
      <article-id pub-id-type="publisher-id">jri10026</article-id>
      <article-id pub-id-type="doi"></article-id>
      <article-id pub-id-type="pmid"></article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
             <subject></subject> 
        </subj-group>
        <subj-group>
            <subject></subject>
        </subj-group> 
      </article-categories>
      <title-group>
        <article-title>Effect of CatSper and Hv1 Channel Inhibition on Progesterone Stimulated Human Sperm</article-title>
      </title-group>
        <contrib-group><contrib contrib-type="author"><name><surname>Keshtgar</surname><given-names>Sara</given-names></name></contrib><aff>Department of Physiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Ghanbari</surname><given-names>Hamideh</given-names></name></contrib><aff>Department of Physiology, Faculty of Medicine, Hormozgan University of Medical Sciences, Bandar Abbas, Iran</aff><aff>Endocrinology and Metabolism Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Ghani</surname><given-names>Esmaeel</given-names></name></contrib><aff>Department of Physiology, Faculty of Medicine, Hormozgan University of Medical Sciences, Bandar Abbas, Iran</aff><aff>Endocrinology and Metabolism Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Shid Moosavi</surname><given-names>Seyed Mostafa</given-names></name></contrib><aff>Department of Physiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran</aff></contrib-group>
      <pub-date pub-type="ppub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <pub-date pub-type="epub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <volume>19</volume>
      <issue>3</issue>
      <fpage>133</fpage>
      <lpage>140</lpage>
      <history>
        <date date-type="received">
          <day>5</day>
          <month>3</month>
          <year>2018</year>
        </date>
        <date date-type="accepted">
          <day>9</day>
          <month>6</month>
          <year>2018</year>
        </date>
      </history>
      <abstract>
      <p>
      &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;

      </p>
      </abstract>
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