<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Physiology and Pharmacology</title>
<title_fa></title_fa>
<short_title>Physiol Pharmacol</short_title>
<subject>Medical Sciences</subject>
<web_url>http://ppj.phypha.ir</web_url>
<journal_hbi_system_id>32</journal_hbi_system_id>
<journal_hbi_system_user>journal32</journal_hbi_system_user>
<journal_id_issn>24765236</journal_id_issn>
<journal_id_issn_online>24765244</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.22034</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>(previous ISSN: 17350581)</journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1390</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2012</year>
	<month>1</month>
	<day>1</day>
</pubdate>
<volume>15</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>Evaluation of the effects of taurine on cisplatin-induced kidney injury and oxidative stress in male rats</title>
	<subject_fa>Renal Physiology/Pharmacology</subject_fa>
	<subject>Renal Physiology/Pharmacology</subject>
	<content_type_fa>Experimental research article</content_type_fa>
	<content_type>Experimental research article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>Introduction: Cisplatin is used as a chemotherapeutic agent for the treatment of human ovarian and testicular
cancers. This study was designed to investigate the protective role of taurine against cisplatin-induced kidney injury.
Methods: Male Wistar rats were divided into 4 groups (n=8) (1) saline-treated group (2) cisplatin-treated group (10
mg/kg, i.p.), (3) group that received taurine (200 mg/kg, i.p) 1 hr before cisplatin (10 mg/kg, i.p) administration and (4)
taurine treated group (200 mg/kg, i.p). The treatment period was 7 days. Animals were then weighed and blood samples
were collected from the heart. After sacrifice, kidneys were removed and kept at -70 °C until further analyses.
Results: Cisplatin significantly elevated the creatinine and blood urea nitrogen (BUN) serum levels (P&lt;0.05). Pretreatment
with taurine resulted in a remarkable reduction of these markers. The catalase activity in cisplatin-treated rats
was significantly decreased (P&lt;0.05) and taurine administration could remarkably recover this decreased activity.
Malondialdehyde (MDA) content of the kidneys was increased in cisplatin-exposed animals and taurine significantly
reduced the amount of MDA.
Conclusion: Our data suggest that pretreatment with taurine might be considered as a protective approach in
cisplatin-induced nephrotoxicity.

</abstract>
	<keyword_fa></keyword_fa>
	<keyword>cisplatin, taurine, kidney injury, rat</keyword>
	<start_page>478</start_page>
	<end_page>485</end_page>
	<web_url>http://ppj.phypha.ir/browse.php?a_code=A-10-438-4&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>maryam</first_name>
	<middle_name></middle_name>
	<last_name>noruzi</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>mery_noruzi@ymail.com</email>
	<code>320031947532846009905</code>
	<orcid>320031947532846009905</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>samad</first_name>
	<middle_name></middle_name>
	<last_name>zareh</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>320031947532846009906</code>
	<orcid>320031947532846009906</orcid>
	<coreauthor>No</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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