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Influence of Silymarin Administration on Hepatic Glutathione-Conjugating Enzyme System in Rats Treated with Antitubercular Drugs

 

作者: Chandrasekaran Victorrajmohan,   Kannampalli Pradeep,   Sivanesan Karthikeyan,  

 

期刊: Drugs in R & D  (ADIS Available online 2005)
卷期: Volume 6, issue 6  

页码: 395-400

 

ISSN:1174-5886

 

年代: 2005

 

出版商: ADIS

 

关键词: Antioxidants, pharmacodynamics;Free radical scavengers, pharmacodynamics;Silymarin, pharmacodynamics

 

数据来源: ADIS

 

摘要:

ObjectiveThis study evaluated the influence of simultaneous administration of silymarin (SIL), a hepatoprotective and antioxidant agent, on the status of glutathione (GSH) and its metabolising enzymes in the liver tissue of rats treated with antitubercular drugs, i.e. isoniazid (INH), rifampicin (RIF) and pyrazinamide (PYR).MethodsMale Wistar albino rats (n = 24) were randomly divided into four groups. Group I received saline as they served as controls. Group II rats were administered antitubercular drugs (INH 25mg/kg + RIF 50mg/kg + PYR 140 mg/kg orally) daily for 45 days. Group III animals were treated with SIL (50 mg/kg orally) simultaneously with the antitubercular drugs for the same period. Group IV animals were treated with SIL alone. The status of GSH, glutathione peroxidase (GPx), glutathione reductase (GR) and glutathione-s-transferase (GST) in liver tissue was evaluated at the end of the study.ResultsAdministration of antitubercular drugs caused a significant decrease (p < 0.001) in the status of GPx, GST and GR and of non-enzymic (GSH) antioxidants in liver tissue when compared with saline-treated control rats. Simultaneous treatment of SIL with antitubercular drugs completely prevented decreases in the levels of all the above parameters. Treatment with SIL alone enhanced the activities of GST (p < 0.001) and GPx (p < 0.05) and did not alter glutathione levels compared with control.ConclusionA fall in the status of glutathione and its conjugating enzymes upon administration of antitubercular drugs denotes an impairment of the antioxidant defence mechanism. Simultaneous administration of SIL afforded complete protection of the liver against this abnormality, an effect that could have been due to the strong antioxidant properties of SIL.

 

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