Protective role of CoQ10 or L-carnitine on the integrity of the myocardium in doxorubicin induced toxicity

Tissue Cell. 2017 Jun;49(3):410-426. doi: 10.1016/j.tice.2017.03.007. Epub 2017 Apr 2.

Abstract

Doxorubicin (DOX) is a chemotherapeutic agent used for treatment of different cancers and its clinical usage is hindered by the oxidative injury-related cardiotoxicity. This work aims to declare if the harmful effects of DOX on heart can be alleviated with the use of Coenzyme Q10 (CoQ10) or L-carnitine. The study was performed on seventy two female Wistar albino rats divided into six groups, 12 animals each: Control group; DOX group (10mg/kg); CoQ10 group (200mg/kg); L-carnitine group (100mg/kg); DOX+CoQ10 group; DOX+L-carnitine group. CoQ10 and L-carnitine treatment orally started 5days before a single dose of 10mg/kg DOX that injected intraperitoneally (IP) then the treatment continued for 10days. At the end of the study, serum biochemical parameters of cardiac damage, oxidative stress indices, and histopathological changes were investigated. CoQ10 or L-carnitine showed a noticeable effects in improving cardiac functions evidenced reducing serum enzymes as serum interleukin-1 beta (IL-1 β), tumor necrosis factor alpha (TNF-α), leptin, lactate dehydrogenase (LDH), Cardiotrophin-1, Troponin-I and Troponin-T. Also, alleviate oxidative stress, decrease of cardiac Malondialdehyde (MDA), Nitric oxide (NO) and restoring cardiac reduced glutathione levels to normal levels. Both corrected the cardiac alterations histologically and ultrastructurally. With a visible improvements in α-SMA, vimentin and eNOS immunohistochemical markers. CoQ10 or L-carnitine supplementation improves the functional and structural integrity of the myocardium.

Keywords: Cardiotoxicity; CoQ10 and L-carnitine; Dox; Vimentin; eNOS.

MeSH terms

  • Animals
  • Cardiotoxicity / metabolism
  • Cardiotoxicity / pathology
  • Cardiotoxicity / prevention & control
  • Carnitine / pharmacology*
  • Doxorubicin / adverse effects*
  • Doxorubicin / pharmacology
  • Female
  • Heart Diseases* / chemically induced
  • Heart Diseases* / metabolism
  • Heart Diseases* / pathology
  • Heart Diseases* / prevention & control
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Oxidative Stress / drug effects*
  • Rats
  • Rats, Wistar
  • Ubiquinone / analogs & derivatives*
  • Ubiquinone / pharmacology

Substances

  • Ubiquinone
  • Doxorubicin
  • coenzyme Q10
  • Carnitine