Journal
ARCHIVES OF MEDICAL RESEARCH
Volume 45, Issue 6, Pages 462-468Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.arcmed.2014.07.006
Keywords
Anticancer drug; Oxidative stress; Biomarker; Liver; Antioxidants; Toxicity
Categories
Funding
- University Grants Commission (UGC), Government of India
- Basic Science Research Senior Research Fellowship of UGC
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Background and Aims. Cisplatin (CP) is regarded as a major anticancer drug against a wide spectrum of leukemia and other malignancies. The mode of action of CP on cancer cells is attributed to its property of releasing free radicals which, at the same time, has the potential to damage liver and kidney cells. The tissue-specific toxicity of CP to the kidneys is well documented. However, there is a paucity of literature on systemic toxicity and also the amelioration of such effect. The aim of the present study was to evaluate the damage caused by CP and its modulation by using the antioxidant capacity of curcumin (CMN, a natural polyphenolic compound) in Wistar rats. Methods. We evaluated the ameliorative effect of CMN (200 mg/kg body weight, b.w.) on the toxicity of CF in rat liver. Oxidative stress biomarkers, enzymatic and nonenzymatic antioxidants were evaluated for assessing the mitigatory potential of CMN against CF-induced toxicity. Results. A single dose of CF (7 mg/kg b.w.) caused marked hepatic damage. CF caused a significant increase in lipid peroxidation (LPO) level and protein carbonyl (PC) content. Pretreatment of rat with CMN significantly restored the LPO levels and PC content. It also replenished the CF-induced modulatory effects on altered enzymatic and nonenzymatic antioxidants in liver. Conclusion. Our results clearly demonstrated that the role of oxidative stress is detrimental in systemic toxicity induced by CF and suggest a mitigatory effect of CMN on CF-induced hepatotoxicity in rat. (C) 2014 IMSS. Published by Elsevier Inc.
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