<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Iranian Biomedical Journal</title>
<title_fa>مجله بیومدیکال ایران</title_fa>
<short_title>IBJ</short_title>
<subject>Basic Sciences</subject>
<web_url>http://ibj.pasteur.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>1028-852X</journal_id_issn>
<journal_id_issn_online>2008-823X</journal_id_issn_online>
<journal_id_pii>-</journal_id_pii>
<journal_id_doi>10.61882/ibj</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>-</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>-</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1400</year>
	<month>4</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2021</year>
	<month>7</month>
	<day>1</day>
</pubdate>
<volume>25</volume>
<number>4</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>Valproic Acid Ameliorates Locomotor Function in the Rat Model of Contusion via Alteration of Mst1, Bcl-2, and Nrf2 Gene Expression</title>
	<subject_fa> Related Fields</subject_fa>
	<subject>Related Fields</subject>
	<content_type_fa>مقاله کوتاه</content_type_fa>
	<content_type>Short Communication</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;strong&gt;Background&lt;/strong&gt;: In animal models of inflammatory diseases, Mammalian sterile 20-like kinase 1 (&lt;em&gt;Mst1)&lt;/em&gt; facilitates the programmed cell death as a novel pro-apoptotic kinase. This research aimed to determine the expression level of &lt;em&gt;Mst1&lt;/em&gt; gene in a rat model of SCI treated with valproic acid (VPA). &lt;strong&gt;Methods: &lt;/strong&gt;Severe rat model contusion was used for evaluation of the neuroprotective effect of valproic acid. The Basso-Beattie-Bresnahan test, was performed to determine locomotor functions. Hematoxylin/eosin staining and TUNEL assay were performed to detect cavity formation and apoptosis, respectively. The mRNA levels of the genes &lt;em&gt;Mst1&lt;/em&gt;, nuclear factor (erythroid-derived 2)-like 2, and B-cell lymphoma 2 were evaluated, using quantitative real-time PCR acute spinal cord injury (RT-PCR). &lt;strong&gt;Results&lt;/strong&gt;: The results revealed that &lt;em&gt;Mst1&lt;/em&gt; gene expression and TUNEL-positive cells in the VPA-treated group were significantly reduced as compared to the untreated group (&lt;em&gt;p&lt;/em&gt; &amp;le; 0.05). &lt;strong&gt;Conclusion&lt;/strong&gt;: Our findings indicate that VPA has therapeutic potential and can be a candidate for the treatment of neurodegenerative disorders and traumatic injury as a promising drug.</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Bcl-2, Contusion, Mst1, Nrf2, Valproic acid</keyword>
	<start_page>303</start_page>
	<end_page>307</end_page>
	<web_url>http://ibj.pasteur.ac.ir/browse.php?a_code=A-10-538-4&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Ali</first_name>
	<middle_name></middle_name>
	<last_name>Mardi</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>ali.mardi66@yahoo.com</email>
	<code></code>
	<orcid>0000-0002-8303-274X</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Molecular Medicine and Genetics, School of Medicine, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Alireza</first_name>
	<middle_name></middle_name>
	<last_name>Biglari</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>biglari@zums.ac.ir</email>
	<code></code>
	<orcid>0000-0002-3020-5889</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Molecular Medicine and Genetics, School of Medicine, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Reza</first_name>
	<middle_name></middle_name>
	<last_name>Nejatbakhsh</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>reza_nejat@yahoo.com</email>
	<code></code>
	<orcid>0000-0002-4469-7466</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Anatomy, School of Medicine, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Alireza</first_name>
	<middle_name></middle_name>
	<last_name>Abdanipour</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>abdani.anatomy@yahoo.com</email>
	<code></code>
	<orcid>0000-0002-2975-3423</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Anatomy, School of Medicine, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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