<?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>1388</year>
	<month>6</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2009</year>
	<month>9</month>
	<day>1</day>
</pubdate>
<volume>2</volume>
<number>3</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>Pentoxifylline Attenuates Malathion-Induced Oxidative Damage in Rat</title_fa>
	<title>Pentoxifylline Attenuates Malathion-Induced Oxidative Damage in Rat</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;span style=&quot;font-weight: bold&quot;&gt;Introduction: &lt;/span&gt;Toxic effects of pesticides are commonly associated with reactive oxygen species damage and pentoxifylline a phosphodiesterase inhibitor is a drug well known for antioxidant properties. The purpose of this study was to evaluate the oxidative damages following a subacute exposure to malathion, an organophosphorus insecticide and pentoxifylline's ability to counteract these effects. &lt;br&gt;&lt;span style=&quot;font-weight: bold&quot;&gt;Material and Methods:&lt;/span&gt; Malathion (200 mg/kg/day) and pentoxifylline (50 mg/kg/day) alone or in combination were administered intraperitoneally to rats and after one week, total antioxidant capacity (TAC) and total thiol groups (TTG) were measured in their blood. &lt;br&gt;&lt;span style=&quot;font-weight: bold&quot;&gt;Results:&lt;/span&gt; Pentoxifylline increased total antioxidant capacity (TAC) and total thiol groups (TTG) in blood significantly compared to malathion which decreased them. &lt;br&gt;&lt;span style=&quot;font-weight: bold&quot;&gt;Conclusion:&lt;/span&gt; Our findings suggest that oxidative stress occurs in exposure to malathion and oxidative damage may be a contributory factor in complications associated with malathion. The results indicate that malathion exposure decreases TAC and TTG, a process involved in oxidative stress and pentoxifylline could prevent this damage. 
</abstract>
	<keyword_fa>Malathion, Oxidative Stress, Pentoxifylline, Antioxidants Analysis, Rats</keyword_fa>
	<keyword>Malathion, Oxidative Stress, Pentoxifylline, Antioxidants Analysis, Rats</keyword>
	<start_page>211</start_page>
	<end_page>215</end_page>
	<web_url>http://ijt.arakmu.ac.ir/browse.php?a_code=A-10-2-45&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Akram </first_name>
	<middle_name></middle_name>
	<last_name>Ranjbar</last_name>
	<suffix></suffix>
	<first_name_fa>اکرم</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>رنجبر</last_name_fa>
	<suffix_fa></suffix_fa>
	<email>a.rangbar@yahoo.com</email>
	<code>10031947532846003335</code>
	<orcid>10031947532846003335</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Toxicology, Hamedan University of Medical Sciences, H amedan, Iran</affiliation>
	<affiliation_fa>Department of Toxicology, Hamedan University of Medical Sciences, H amedan, Iran</affiliation_fa>
	 </author>


	<author>
	<first_name>Rezvan</first_name>
	<middle_name></middle_name>
	<last_name>Salehidoost</last_name>
	<suffix></suffix>
	<first_name_fa>رضوان</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>صالحی دوست</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846003336</code>
	<orcid>10031947532846003336</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Shariati Hospital Tehran University of Medical sciences, Tehran. Iran</affiliation>
	<affiliation_fa>Shariati Hospital Tehran University of Medical sciences, Tehran. Iran</affiliation_fa>
	 </author>


	<author>
	<first_name>Maryam </first_name>
	<middle_name></middle_name>
	<last_name>Baeeri</last_name>
	<suffix></suffix>
	<first_name_fa>مریم</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>بعیری</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846003337</code>
	<orcid>10031947532846003337</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Laboratory of Toxicology, Faculty of Pharmacy, and Pharmaceutical Sciences Research Center</affiliation>
	<affiliation_fa>Laboratory of Toxicology, Faculty of Pharmacy, and Pharmaceutical Sciences Research Center</affiliation_fa>
	 </author>


	<author>
	<first_name>Mohammad</first_name>
	<middle_name></middle_name>
	<last_name>Abdollahi</last_name>
	<suffix></suffix>
	<first_name_fa>محمد</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>عبدالهی</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846003338</code>
	<orcid>10031947532846003338</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Laboratory of Toxicology, Faculty of Pharmacy, and Pharmaceutical Sciences Research Center</affiliation>
	<affiliation_fa>Laboratory of Toxicology, Faculty of Pharmacy, and Pharmaceutical Sciences Research Center</affiliation_fa>
	 </author>


</author_list>


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