Combined treatment of epigallocatechin gallate and Coenzyme Q10 attenuates cisplatin-induced nephrotoxicity via suppression of oxidative/nitrosative stress, inflammation and cellular damage

Sabiha Fatima, Noura Al-Mohaimeed, Yazeed Al-Shaikh, Poonam Tyagi, Naheed Banu, Shirin Hasan, Sadia Arjumand

Research output: Contribution to journalArticlepeer-review

44 Scopus citations

Abstract

Cisplatin (CP), a platinum based anticancer drug is used as one of the first-line therapy for the treatment of different types of solid tumors. However, CP-induced side effects particularly, nephrotoxicity is a major concern. A single nephrotoxic dose (7 mg/kg body weight) of CP was administered in rats with or without, pre and post combined multidoses of epigallocatechin gallate (EGCG) and coenzyme Q10 (CoQ10) (15 and 5 mg/kg body weight respectively). CP administration resulted in marked increase in the nephrotoxic parameters with alterations in the oxidative and nitrosative stress markers. The concentration of inflammatory, as well as apoptotic markers were markedly up-regulated in the kidney of the CP-treated group. Furthermore, CP resulted in histological injury in the renal tissues. Combined antioxidant treatment significantly (p < 0.01) attenuated CP-induced oxidative stress, nitrosative stress, inflammatory and apoptotic parameters. Moreover, an improvement in the histopathological changes confirmed the nephroprotective effect of antioxidant treatment. In conclusion, our study indicates that the combinatorial multidoses of EGCG and CoQ10 ameliorate the cisplatin-mediated pathogenesis by improving renal oxidative/nitrosative status, inflammation and apoptosis and thus can be used as a promising protective agent to increase the efficacy of the drug by minimizing its major side effect i.e. nephrotoxicity.

Original languageEnglish
Pages (from-to)213-220
Number of pages8
JournalFood and Chemical Toxicology
Volume94
DOIs
StatePublished - 1 Aug 2016
Externally publishedYes

Keywords

  • Apoptosis
  • Cisplatin
  • Coenzyme Q10
  • EGCG
  • Inflammation
  • Nephrotoxicity
  • Oxidative stress/nitrosative stress

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