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									<identifier>oai:www.peertechzpublications.org:10.17352/gjbbs.000005</identifier>
									<datestamp>2016-02-22</datestamp>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Ruta graveolens Protects Against Isoniazid/Rifampicin-Induced Nephrotoxicity through Modulation of Oxidative Stress and Inflammation
										</dc:title><dc:creator>Ayman M Mahmoud</dc:creator><dc:creator> Omnia E Hussein</dc:creator><dc:creator> Mousa O Germoush</dc:creator><dc:description>&lt;p&gt;&lt;strong&gt;Background and Aim&lt;/strong&gt; Drug-induced nephrotoxicity is a renal dyfunction that arises as a result of exposure to nephrotoxic drugs. Anti-tuberculosis therapy can cause nephrotoxicity and permanent kidney&amp;nbsp; damage. The&amp;nbsp; current&amp;nbsp; study&amp;nbsp; was&amp;nbsp; designed&amp;nbsp; to&amp;nbsp; evaluate&amp;nbsp; the&amp;nbsp; possible&amp;nbsp; protective&amp;nbsp; effects&amp;nbsp; of Ruta graveolens L. leaves extract against isoniazid/rifampicin-induced nephrotoxicity in rats.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods&lt;/strong&gt;:The experimental rats received isoniazid and rifampicin at dose level of 50 mg/kg, and 50 or 100 mg/kg/day Ruta graveolens leaves extract orally for 45 days.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Isoniazid/ rifampicin administration induced kidney injury evidenced by the histopathological alterations as well as significant (P&amp;lt;0.001) increase in serum creatinine, urea and uric acid. soniazid/rifampicin-intoxicated rats exhibited a significant increase in serum tumor necrosis factor alpha (P&amp;lt;0.001), and renal lipid peroxidation (P&amp;lt;0.01) and nitric oxide (P&amp;lt;0.001) levels. On the other hand, reduced glutathione level, and activity of superoxide dismutase and glutathione peroxidase were&amp;nbsp; markedly&amp;nbsp; (P&amp;lt;0.001)&amp;nbsp; declined&amp;nbsp; in&amp;nbsp; kidney&amp;nbsp; of&amp;nbsp; isoniazid/rifampicin-induced rats.Concomitant supplementation&amp;nbsp; with&amp;nbsp; either&amp;nbsp; 50 or 100&amp;nbsp; mg/kg&amp;nbsp; dose&amp;nbsp; of Ruta&amp;nbsp; graveolens&amp;nbsp; leaves&amp;nbsp; extract&amp;nbsp; prevented&amp;nbsp; the isoniazid/rifampicin-induced biochemical and histopathological alterations. &lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt;The present investigation confers new information on the protective mechanism of Ruta graveolens leaves extract on anti-tuberculosis therapy-induced nephrotoxicity.Ruta graveolens protects&amp;nbsp; against isoniazid/rifampicin-induced renal injury through attattenuation of inflammation and oxidative stress, and potentiation of the antioxidant defense system.&lt;/p&gt;</dc:description>
										<dc:publisher>Global Journal of Biotechnology and Biomaterial Science - Peertechz Publications</dc:publisher>
										<dc:date>2016-02-22</dc:date>
										<dc:type>Research Article</dc:type>
										<dc:identifier>https://doi.org/10.17352/gjbbs.000005</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Ayman M Mahmoud et al.</dc:rights>
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