A Novel Angiotensin Type I Receptor Antagonist, Fimasartan, Prevents Doxorubicin-induced Cardiotoxicity in Rats

J Korean Med Sci. 2015 May;30(5):559-68. doi: 10.3346/jkms.2015.30.5.559. Epub 2015 Apr 15.

Abstract

Angiotensin receptor blockers (ARBs) have organ-protective effects in heart failure and may be also effective in doxorubicin-induced cardiomyopathy (DOX-CMP); however, the efficacy of ARBs on the prevention of DOX-CMP have not been investigated. We performed a preclinical experiment to evaluate the preventive effect of a novel ARB, fimasartan, in DOX-CMP. All animals underwent echocardiography and were randomly assigned into three groups: treated daily with vehicle (DOX-only group, n=22), 5 mg/kg of fimasartan (Low-fima group, n=22), and 10 mg/kg of fimasartan (High-fima group, n=19). DOX was injected once a week for six weeks. Echocardiography and hemodynamic assessment was performed at the 8th week using a miniaturized conductance catheter. Survival rate of the High-fima group was greater (100%) than that of the Low-fima (75%) and DOX-only groups (50%). Echocardiography showed preserved left ventricular (LV) ejection fraction in the High-fima group, but not in the DOX-only group (P=0.002). LV dimensions increased in the DOX-only group; however, remodeling was attenuated in the Low-fima and High-fima groups. Hemodynamic assessment showed higher dP/dt in the High-fima group compared with the DOX-only group. A novel ARB, fimasartan, may prevent DOX-CMP and improve survival rate in a dose-dependent manner in a rat model of DOX-CMP and could be a treatment option for the prevention of DOX-CMP.

Keywords: Angiotensin Receptor Blocker; Doxorubicin-induced Cardiomyopathy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin Receptor Antagonists / therapeutic use*
  • Animals
  • Biphenyl Compounds / therapeutic use*
  • Cardiomyopathies / chemically induced
  • Cardiomyopathies / mortality
  • Cardiomyopathies / prevention & control*
  • Doxorubicin / toxicity*
  • Echocardiography
  • Hemodynamics
  • Pyrimidines / therapeutic use*
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Angiotensin, Type 1 / chemistry
  • Receptor, Angiotensin, Type 1 / metabolism*
  • Survival Rate
  • Tetrazoles / therapeutic use*
  • Ventricular Function, Left / physiology

Substances

  • Angiotensin Receptor Antagonists
  • Biphenyl Compounds
  • Pyrimidines
  • Receptor, Angiotensin, Type 1
  • Tetrazoles
  • Doxorubicin
  • fimasartan