Protective effect of Co-enzyme Q10 On doxorubicin-induced cardiomyopathy of rat hearts

Environ Toxicol. 2017 Feb;32(2):679-689. doi: 10.1002/tox.22270. Epub 2016 Apr 18.

Abstract

Q10 is a powerful antioxidant often used in medical nutritional supplements for cancer treatment. This study determined whether Q10 could effectively prevent cardio-toxicity caused by doxorubicin treatment. Four week old SD rats were segregated into groups namely control, doxorubicin group (challenged with doxorubicin), Dox + Q10 group (with doxorubicin challenge and oral Q10 treatment), and Q10 group (with oral Q10 treatment). Doxorubicin groups received IP doxorubicin (2.5 mg/kg) every 3 days and Q10 groups received Q10 (10 mg/kg) every day. Three weeks of doxorubicin challenge caused significant reduction in heart weight, disarray in cardiomyocyte arrangement, elevation of collagen accumulation, enhancement of fibrosis and cell death associated proteins, and inhibition of survival proteins. However, Q10 effectively protected cardiomyocytes and ameliorated fibrosis and cell death induced by doxorubicin. Q10 is, therefore, evidently a potential drug to prevent heart damage caused by doxorubicin. © 2016 Wiley Periodicals, Inc. Environ Toxicol 32: 679-689, 2017.

Keywords: cardiac apoptosis; cardiac fibrosis; cardio-toxicity; coenzyme Q10.

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic / adverse effects*
  • Antioxidants / pharmacology
  • Apoptosis / drug effects
  • Cardiomyopathies / chemically induced
  • Cardiomyopathies / prevention & control*
  • Cardiotonic Agents / pharmacology*
  • Cell Survival / drug effects
  • Doxorubicin / adverse effects*
  • Male
  • Myocytes, Cardiac / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Ubiquinone / analogs & derivatives*
  • Ubiquinone / pharmacology

Substances

  • Antibiotics, Antineoplastic
  • Antioxidants
  • Cardiotonic Agents
  • Ubiquinone
  • Doxorubicin
  • coenzyme Q10