Resveratrol improves survival, hemodynamics and energetics in a rat model of hypertension leading to heart failure

PLoS One. 2011;6(10):e26391. doi: 10.1371/journal.pone.0026391. Epub 2011 Oct 18.

Abstract

Heart failure (HF) is characterized by contractile dysfunction associated with altered energy metabolism. This study was aimed at determining whether resveratrol, a polyphenol known to activate energy metabolism, could be beneficial as a metabolic therapy of HF. Survival, ventricular and vascular function as well as cardiac and skeletal muscle energy metabolism were assessed in a hypertensive model of HF, the Dahl salt-sensitive rat fed with a high-salt diet (HS-NT). Resveratrol (18 mg/kg/day; HS-RSV) was given for 8 weeks after hypertension and cardiac hypertrophy were established (which occurred 3 weeks after salt addition). Resveratrol treatment improved survival (64% in HS-RSV versus 15% in HS-NT, p<0.001), and prevented the 25% reduction in body weight in HS-NT (P<0.001). Moreover, RSV counteracted the development of cardiac dysfunction (fractional shortening -34% in HS-NT) as evaluated by echocardiography, which occurred without regression of hypertension or hypertrophy. Moreover, aortic endothelial dysfunction present in HS-NT was prevented in resveratrol-treated rats. Resveratrol treatment tended to preserve mitochondrial mass and biogenesis and completely protected mitochondrial fatty acid oxidation and PPARα (peroxisome proliferator-activated receptor α) expression. We conclude that resveratrol treatment exerts beneficial protective effects on survival, endothelium-dependent smooth muscle relaxation and cardiac contractile and mitochondrial function, suggesting that resveratrol or metabolic activators could be a relevant therapy in hypertension-induced HF.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Weight / drug effects
  • Disease Models, Animal
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / pathology
  • Energy Metabolism / drug effects*
  • Heart / drug effects
  • Heart / physiopathology
  • Heart Failure / etiology
  • Heart Failure / metabolism*
  • Heart Failure / pathology
  • Heart Failure / physiopathology*
  • Hemodynamics / drug effects*
  • Hypertension / complications*
  • Male
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Rats
  • Rats, Inbred Dahl
  • Resveratrol
  • Signal Transduction / drug effects
  • Stilbenes / pharmacology*
  • Survival Analysis

Substances

  • Stilbenes
  • Resveratrol