<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Iranian Journal of Fisheries Sciences</title>
<title_fa>مجله علوم شیلاتی ایران</title_fa>
<short_title>IJFS</short_title>
<subject>Agriculture</subject>
<web_url>http://jifro.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>1562-2916</journal_id_issn>
<journal_id_issn_online>2322-5696</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.18869/acadpub.ijfs</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1399</year>
	<month>8</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2020</year>
	<month>11</month>
	<day>1</day>
</pubdate>
<volume>19</volume>
<number>6</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Research Article: A rapid approach to assess estrogenic transcriptional activity of bisphenol A in the liver of goldfish</title>
	<subject_fa>Biology &amp; physiology</subject_fa>
	<subject>Biology &amp; physiology</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Orginal research papers</content_type>
	<abstract_fa></abstract_fa>
	<abstract>Bisphenol A (BPA) is a synthetic compound widely used in types of consumer goods and medical tools. It has been shown that BPA acts as an endocrine disruptor chemical casuing negative impact on reproductive functions. The present study used an &lt;em&gt;in vitro&lt;/em&gt; approach to assess estrogenic transcriptional activity of BPA as a rapid and sensitive method. The cultured pieces of hepatic tissue of goldfish (&lt;em&gt;Carassius auratus&lt;/em&gt;) were exposed to 1, 5, 25 &amp;mu;g L&lt;sup&gt;-1&lt;/sup&gt; BPA and 1 &amp;mu;g L&lt;sup&gt;-1&lt;/sup&gt; E&lt;sub&gt;2&lt;/sub&gt; for comparison over 24 h. Compared to control, the mRNA transcript of &lt;em&gt;er&amp;beta;-I&lt;/em&gt; showed a significant increase in the hepatic tissues exposed to all doses of BPA and E&lt;sub&gt;2&lt;/sub&gt;. The mRNA transcript of &lt;em&gt;er&amp;beta;-II&lt;/em&gt; was signifincantly increased in hepatic tissues exposed to 1 and 5 &amp;mu;g L&lt;sup&gt;-1&lt;/sup&gt; BPA and E&lt;sub&gt;2&lt;/sub&gt;. The mRNA transcripts of &lt;em&gt;vtg&lt;/em&gt; in the hepatic tissues treated with 5 &amp;mu;g L&lt;sup&gt;-1&lt;/sup&gt; BPA and E&lt;sub&gt;2&lt;/sub&gt; were also increased, significantly. Finally, &lt;em&gt;cyp1a&lt;/em&gt; mRNA transcript showed a significant increase in the hepatic tissues exposed to 5 and 25 &amp;mu;g L&lt;sup&gt;-1&lt;/sup&gt; BPA and E&lt;sub&gt;2&lt;/sub&gt;. These results show an estrogenic activity of BPA similar to E&lt;sub&gt;2&lt;/sub&gt;, and suggest that &lt;em&gt;in vitro&lt;/em&gt; approach can be used as an alternative to &lt;em&gt;in vivo&lt;/em&gt; test to detect estrogenic effects of BPA.&lt;br&gt;
&amp;nbsp;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>BPA, Esterogenic activity, Vitellogenin, mRNA transcript</keyword>
	<start_page>2877</start_page>
	<end_page>2892</end_page>
	<web_url>http://jifro.ir/browse.php?a_code=A-10-2686-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>M.</first_name>
	<middle_name></middle_name>
	<last_name>Golshan</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>mahdigolshan@yahoo.com</email>
	<code>100319475328460038302</code>
	<orcid>100319475328460038302</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Iranian Fisheries Science Research Institute, Agricultural Research, Education and Extension Organization</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>A.</first_name>
	<middle_name></middle_name>
	<last_name>Hatef</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>azadeh.hatef@usask.ca</email>
	<code>100319475328460038303</code>
	<orcid>100319475328460038303</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Laboratory of Integrative Neuroendocrinology, Department of Veterinary Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>H.R.</first_name>
	<middle_name></middle_name>
	<last_name>Habibi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>habibi@ucalgary.ca</email>
	<code>100319475328460038304</code>
	<orcid>100319475328460038304</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Biological Sciences, University of Calgary</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>S.M.H.</first_name>
	<middle_name></middle_name>
	<last_name>Alavi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>hadi.alavi@ut.ac.ir</email>
	<code>100319475328460038305</code>
	<orcid>100319475328460038305</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>School of Biology, College of Science, University of Tehran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
