Article

Protective effect of alpha-lipoic acid against chloroquine-induced hepatotoxicity in rats.

Department of Biochemistry, Faculty of Science, Annamalai University, Annamalai Nagar, Tamil Nadu 608 002, India.
Journal of Applied Toxicology (impact factor: 2.48). 24(1):21-6. DOI:10.1002/jat.940 pp.21-6
Source: PubMed

ABSTRACT Oral administration of a-lipoic acid, a metavitamin, was investigated for its possible hepatoprotective effect in Wistar rats against chloroquine-induced toxicity. Rats were treated orally with alpha-lipoic acid (10, 30 and 100 mg x kg(-1) day(-1)) for 7 days before a single oral administration of chloroquine (970 mg x kg(-1) day(-1)) and alpha-lipoic acid treatment was continued for three more days. The increased level of serum enzymes (aspartate transaminase, alanine transaminase and alkaline phosphatase), bilirubin, lipids and plasma thiobarbituric acid-reactive substances (TBARS) and hydroperoxides observed in rats treated with chloroquine were very much reduced in rats treated with alpha-lipoic acid plus chloroquine. A significant decrease in plasma antioxidants such as reduced glutathione (GSH), vitamin C and vitamin E were observed in chloroquine-treated rats when compared with control rats. Administration of alpha-lipoic acid significantly improved the levels of plasma antioxidants GSH, vitamin C and vitamin E in chloroquine-treated rats. In the case of 100 mg x kg(-1) day(-1) the effect was highly significant compared with the other doses (10 and 30 mg x kg(-1) day(-1)). The results of the study revealed that alpha-lipoic acid could offer protection against chloroquine-induced hepatotoxicity. alpha-Lipoic acid had a better protective effect when compared with silymarin, a reference drug.

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Keywords

7 days
 
alanine transaminase
 
alpha-lipoic acid
 
alpha-lipoic acid treatment
 
aspartate transaminase
 
chloroquine-induced hepatotoxicity
 
chloroquine-induced toxicity
 
chloroquine-treated rats
 
control rats
 
Oral administration
 
plasma thiobarbituric acid-reactive substances
 
possible hepatoprotective effect
 
protective effect
 
reference drug
 
serum enzymes
 
significant decrease
 
single oral administration
 
vitamin C
 
vitamin E
 
Wistar rats