Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/4564
Title: Modulation of CYP4502E1 and oxidative stress by testosterone in liver and kidney of benzene treated rats
Authors: Verma, Yeshvandra
Rana, S V S
Keywords: Benzene;Castration;GSH;Kidney;Liver;Lipid peroxidation;Testosterone
Issue Date: Aug-2008
Publisher: CSIR
Abstract: Bilateral castration increased lipid peroxidation and consequently reduced glutathione in both liver and kidney. Testosterone administration reduced lipid peroxidation in the liver of castrated and benzene treated rats, however, reduced glutathione status could not be restored. Benzene depleted CYP4502E1 in castrated rats, however, the enzyme was restored in liver and kidney both after testosterone treatment. The results suggest that testosterone affects the metabolism and disposition of benzene by influencing CYP4502E1. Other hormonal and cellular/molecular factors may also alter the actions of testosterone. Testosterone dependent mechanism of toxicity of benzene in the liver and kidney has been discussed.
Page(s): 568-572
URI: http://hdl.handle.net/123456789/4564
ISSN: 0975-1009 (Online); 0019-5189 (Print)
Appears in Collections:IJEB Vol.46(08) [August 2008]

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