<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Iranian Journal of Toxicology</title>
<title_fa>مجله سم شناسی و مسمومیتهای ایران</title_fa>
<short_title>IJT</short_title>
<subject>Medical Sciences</subject>
<web_url>http://ijt.arakmu.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>2008-2967</journal_id_issn>
<journal_id_issn_online>2251-9459</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>10.22034/IJT</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1398</year>
	<month>7</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2019</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<volume>13</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>Eryngium Bungei Boiss Extract Has Hepatoprotective Effect Against Liver Damage Induced by Acetaminophen in Rats: Novel Antioxidant and Anti-Inflammatory Effects</title>
	<subject_fa>عمومى</subject_fa>
	<subject>General</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Research</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;strong&gt;Background&lt;/strong&gt;: Acetaminophen-induced toxicity is a common cause of acute liver failure. This study investigated the hepatoprotective effects of &lt;em&gt;Eryngium bungei B&lt;/em&gt;oiss (EB) extract against the hepatotoxicity in rats.&lt;br&gt;
&lt;strong&gt;Methods&lt;/strong&gt;: Thirty adult male rats were randomly assigned to five groups, with free access to water and food. They were treated as follows: &lt;em&gt;Group 1&lt;/em&gt; (negative controls): distilled water (DW); &lt;em&gt;Group 2&lt;/em&gt; (positive controls): DW for 7 days and a single dose of 500 mg/kg BW acetaminophen orally on day 8&lt;sup&gt;th&lt;/sup&gt;; &lt;em&gt;Groups 3, 4 &lt;/em&gt;and&lt;em&gt; 5&lt;/em&gt; (experimental groups): received EB extract mixed in DW at 100, 200 and 400 mg/kg/day orally for 7 days plus 500 mg/kg acetaminophen on the 8&lt;sup&gt;th&lt;/sup&gt; day. On the 9thday, blood and liver samples were collected from all rats.&lt;br&gt;
&lt;strong&gt;Results&lt;/strong&gt;: The EB extract improved the adverse histological changes in the rats&amp;rsquo; livers and resulted in reduced serum ALT and ALP enzymes. Oxidative stress was noted in the liver tissue in &lt;em&gt;Group 2&lt;/em&gt;. Pretreatment with EB extract reduced MDA concentration and increased GSH levels, compared to that for &lt;em&gt;Group 2&lt;/em&gt;. The extract at 200 and 400 mg/kg/day significantly increased SOD activity, compared to that for &lt;em&gt;Group 2&lt;/em&gt;. The IL-1&amp;beta; and TNF-&amp;alpha; levels increased significantly in &lt;em&gt;Group 2&lt;/em&gt;, compared to those in &lt;em&gt;Group 1&lt;/em&gt;. Administration of EB extract in Groups 3, 4 and 5 significantly decreased the IL-1&amp;beta; and TNF-&amp;alpha; parameters.&lt;br&gt;
&lt;strong&gt;Conclusions&lt;/strong&gt;: The hepatoprotective effects of EB extract appears to be linked to its glutathione-mediated detoxification, free radical scavenging and anti-inflammatory properties.</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Acetaminophen Hepatotoxicity, Eryngium Bungei Extract, Inflammation, Oxidative Stress, Rats</keyword>
	<start_page>11</start_page>
	<end_page>16</end_page>
	<web_url>http://ijt.arakmu.ac.ir/browse.php?a_code=A-10-604-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Maryam</first_name>
	<middle_name></middle_name>
	<last_name> Fatemi </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></email>
	<code>100319475328460011515</code>
	<orcid>100319475328460011515</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Basic Sciences, School of Veterinary Medicine, Shiraz University. Shiraz, Iran.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Tahoora </first_name>
	<middle_name></middle_name>
	<last_name>Shomali</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>tshomali@shirazu.ac.ir</email>
	<code>100319475328460011516</code>
	<orcid>100319475328460011516</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Basic Sciences, School of Veterinary Medicine, Shiraz University. Shiraz, Iran.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Saeed </first_name>
	<middle_name></middle_name>
	<last_name>Nazifi </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></email>
	<code>100319475328460011517</code>
	<orcid>100319475328460011517</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Clinical Studies, School of Veterinary Medicine, Shiraz University. Shiraz, Iran.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mehdi </first_name>
	<middle_name></middle_name>
	<last_name>Fazeli </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></email>
	<code>100319475328460011518</code>
	<orcid>100319475328460011518</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Basic Sciences, School of Veterinary Medicine, Shiraz University. Shiraz, Iran.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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