Attenuation of oxidative stress and cardiac dysfunction by bisoprolol in an animal model of dilated cardiomyopathy

Biochem Biophys Res Commun. 2006 Nov 10;350(1):105-13. doi: 10.1016/j.bbrc.2006.09.026. Epub 2006 Sep 18.

Abstract

Oxidative stress is an important susceptibility factor for dilated cardiomyopathy. We have investigated the effects of bisoprolol, a beta1-selective adrenoceptor blocker, on oxidative stress and the development of cardiac dysfunction in a model of dilated cardiomyopathy. Male TO-2 and control hamsters at 8 weeks of age were treated with bisoprolol (5 mg/kg per day) or vehicle for 4 weeks. Treatment with bisoprolol prevented the progression of cardiac dysfunction in TO-2 hamsters. This drug did not affect the increase in NADPH oxidase activity but prevented the reduction in activity and expression of mitochondrial manganese-dependent superoxide dismutase as well as the increases in the concentrations of interleukin-1beta and tumor necrosis factor-alpha in the left ventricle of TO-2 hamsters. Attenuation of the development of cardiac dysfunction by bisoprolol may thus result in part from normalization of the associated increases in the levels of oxidative stress and pro-inflammatory cytokines in the left ventricle.

MeSH terms

  • Aldehydes / metabolism
  • Animals
  • Antioxidants / metabolism
  • Bisoprolol / pharmacology*
  • Blood Pressure / drug effects
  • Body Weight / drug effects
  • Cardiomyopathy, Dilated / chemically induced*
  • Cardiomyopathy, Dilated / metabolism
  • Cardiomyopathy, Dilated / pathology
  • Cardiomyopathy, Dilated / physiopathology*
  • Cricetinae
  • Disease Models, Animal*
  • Echocardiography
  • Fibrosis / metabolism
  • Fibrosis / pathology
  • Glutathione / analogs & derivatives
  • Glutathione / metabolism
  • Heart Failure / chemically induced*
  • Heart Failure / metabolism
  • Heart Failure / pathology
  • Heart Failure / physiopathology*
  • Heart Rate / drug effects
  • Interleukin-1 / metabolism
  • Isoenzymes / metabolism
  • Male
  • NADPH Oxidases / metabolism
  • Organ Size / drug effects
  • Oxidative Stress / drug effects*
  • Superoxide Dismutase / metabolism
  • Tumor Necrosis Factor-alpha / metabolism
  • Tyrosine / analogs & derivatives
  • Tyrosine / metabolism
  • Ventricular Function, Left

Substances

  • Aldehydes
  • Antioxidants
  • Interleukin-1
  • Isoenzymes
  • Tumor Necrosis Factor-alpha
  • 3-nitrotyrosine
  • Tyrosine
  • Superoxide Dismutase
  • NADPH Oxidases
  • Glutathione
  • 4-hydroxy-2-nonenal
  • Bisoprolol