Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/23237
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dc.contributor.authorHemieda, Faried A E-
dc.contributor.authorAbdei-Hady, El-Sayed K-
dc.contributor.authorElnga, Mostafa A Abou-
dc.date.accessioned2013-11-11T09:54:43Z-
dc.date.available2013-11-11T09:54:43Z-
dc.date.issued2005-09-
dc.identifier.issn0975-1009 (Online); 0019-5189 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/23237-
dc.description782-785en_US
dc.description.abstractThis study was designed to investigate the hepatotoxicity of ranitidine treatment in dose levels of 10, 30, and 50 mg/kg b.wt. for 3 weeks period in male rats. The results showed some adverse changes in rats treated with either 10 or 30 mg/kg. Treatment with dose of 50 mg/kg produced marked increase in the activity of both acid phosphatase in liver and aspartate aminotransferase in serum and liver, with a tendency for increase in serum alanine aminotransferase activity. Also, a significant decrease in the serum activity of both amylase and alkaline phosphatase was noted. Microscopic examination of livers of the same animals revealed absence of some hepatic cells, pyknotic nuclei, dilatation of blood sinusoids, binucleated cells, and infiltration of lymphocytes. These biochemical and histological changes indicate that ranitidine when given chronically in high dose could produce hepatotoxicity in rats.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJEB Vol.43(09) [September 2005]en_US
dc.subjectACPen_US
dc.subjectALTen_US
dc.subjectASTen_US
dc.subjectHepatotoxicityen_US
dc.subjectRanitidineen_US
dc.subjectRatsen_US
dc.subjectSerumen_US
dc.titleBiochemical and histological studies on H2-receptor antagonist ranitidine-induced hepatotoxicity in ratsen_US
dc.typeArticleen_US
Appears in Collections:IJEB Vol.43(09) [September 2005]

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