<?xml version="1.0" encoding="UTF-8" ?>

    <journal>
    <language>en</language>
    <journal_id_issn>2008-2835</journal_id_issn>
    <journal_id_issn_online>2008-4625</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>276</journal_id_iranmedex>
    <journal_id_magiran>5669</journal_id_magiran>
    <journal_id_sid>11181</journal_id_sid>
    <pubdate>
	    <type>gregorian</type>
	    <year>>2018</year>
	    <month>>October-December</month>
	    <day></day>
    </pubdate>
    <volume>10</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_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>30555653</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>Effects of Dietary Polyunsaturated Fatty Acids on DNA Methylation and the Expression of DNMT3b and PPARα Genes in Rats</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: Previous studies have suggested a protective role for Polyunsaturated Fatty Acids (PUFA) against cancer, cardiovascular, and other diseases. To provide new insights into the&lt;em&gt; in vivo&lt;/em&gt; effects of PUFA on gene expression, the effects of dietary PUFA on &lt;em&gt;DNMT3b&lt;/em&gt; and &lt;em&gt;PPAR&amp;alpha;&lt;/em&gt; gene expression and global DNA methylation were investigated in selected rat tissues.&amp;nbsp;&lt;br /&gt;
Methods: Thirty sprague-dawley rats were allotted into 3 dietary groups of ten animals each, received experimental diets containing PUFAs every day by gavages for 12 weeks as follows: control group fed a normal diet and water; n-3 PUFAs group received 300 &lt;em&gt;mg/kg/day&lt;/em&gt; n-3 PUFAs supplementation; mixed-PUFAs group received 300 &lt;em&gt;mg/kg/day&lt;/em&gt; of a mixture of n-3, -6, -9 PUFAs supplementations. The expressions of &lt;em&gt;DNMT3b&lt;/em&gt; and &lt;em&gt;PPAR&amp;alpha;&lt;/em&gt; genes were quantitated using real-time RT-PCR. The genome-wide 5-methylcytosine contents in rat tissues were determined by ELISA method.&amp;nbsp;&lt;br /&gt;
Results: The average expression of the &lt;em&gt;DNMT3b &lt;/em&gt;mRNA was 50% lower in the colon and liver of rats fed the n-3- or mixed-PUFAs supplemented diet than control group (p=0.00). However, &lt;em&gt;PPAR&amp;alpha;&lt;/em&gt; expression was significantly upregulated both in the colon and liver of PUFAs-supplemented rats (p&amp;lt;0.001). No significant difference was observed in the blood, colon, and liver DNA methylation levels between PUFAs-supplemented and control animals.&lt;br /&gt;
Conclusion: The results indicate that dietary PUFAs could modulate the expressions of &lt;em&gt;PPAR&amp;alpha;&lt;/em&gt; and &lt;em&gt;DNMT3b&lt;/em&gt; genes in various rat tissues. The findings of this study provide additional insights into the in vivo mechanism of PUFA-mediated regulation of gene expression and could provide an opportunity to develop personalized diets for related disease control.&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>DNA methylation, Gene expression, Dietary supplement regulation, Fatty acids omega-3</keyword>
	<start_page>214</start_page>
	<end_page>219</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=325</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/325.pdf</pdf_url>
	<author_list><author><first_name>Ehsan</first_name><middle_name></middle_name><last_name>Maktoobian Baharanchi</last_name><suffix></suffix><affiliation>Department of Biochemistry, Faculty 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>1307</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Mostafa</first_name><middle_name></middle_name><last_name>Moradi Sarabi</last_name><suffix></suffix><affiliation>Department of Biochemistry, Faculty 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>1308</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Fakhraddin</first_name><middle_name></middle_name><last_name>Naghibalhossaini</last_name><suffix></suffix><affiliation>Autoimmune Research Center, Faculty 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>1309</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

