Influence of DL α-lipoic acid and vitamin-E against doxorubicin-induced biochemical and histological changes in the cardiac tissue of rats
Objective: The present study was undertaken to find out the preventive and curative role of lipoic acid (LA) and vitamin E (Vit. E) on doxorubicin (DOX)-induced oxidative stress and to make comparative evaluation between LA and vitamin E in this regard. Materials and Methods: Wistar albino rats were...
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Veröffentlicht in: | Indian journal of pharmacology 2005, Vol.37 (5), p.294 |
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Sprache: | eng |
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Zusammenfassung: | Objective: The present study was undertaken to find out the preventive
and curative role of lipoic acid (LA) and vitamin E (Vit. E) on
doxorubicin (DOX)-induced oxidative stress and to make comparative
evaluation between LA and vitamin E in this regard. Materials and
Methods: Wistar albino rats were used in this experiment. DOX was
administered intraperitoneally in six equal injections (each containing
2.5 mg/kg DOX at 48 h interval) to a total cumulative dose of 15 mg/kg
over a period of 2 weeks to produce cardiotoxicity. Lipoic acid and
vitamin E were administered as pretreatment and post-treatment. The
biochemical parameters such as tissue glutathione (GSH),
malondialdehyde (MDA), lactate dehydrogenase (LDH), catalase (CAT),
superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione
reductase (GR), glutathione-s-transferase (GST), and
glucose-6-phosphate dehydrogenase (G6PD) were monitored after 30 days.
Results: Post-treatment with lipoic acid and vitamin E significantly
protected the myocardium from the toxic effects of DOX, by reducing the
levels of antioxidant enzymes such as CAT, SOD, GPx, GST, and G6PD
towards normal and decreased the increased levels of malondialdehyde.
It has also reduced the severity of cellular damage of the myocardium.
The restoration of the endogenous antioxidant system clearly depicts
that lipoic acid and vitamin E have produced their protective effect by
scavenging the reactive oxygen species (ROS). Pretreatment with LA did
not alter DOX-induced changes of histopathological parameters.
Pretreatment with vitamin E has significantly increased the levels of
blood and tissue GSH and significantly decreased the levels of MDA as
compared to DOX-treated group. Vitamin E has significantly reduced the
activities of the antioxidant enzymes except GSHR as compared to the
DOX-treated group. Conclusion: The study strongly supports the use of
these antioxidants in the treatment of DOX-induced cardiotoxicity;
however, vitamin E is better for both preventive and curative therapy
but LA can be used only for curative therapy. |
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ISSN: | 0253-7613 |
DOI: | 10.4103/0253-7613.16852 |