[Association between beta3-adrenergic receptor and oxidative stress in chronic heart failure rats]

Zhonghua Xin Xue Guan Bing Za Zhi. 2010 May;38(5):435-9.
[Article in Chinese]

Abstract

Objective: To investigate the association between beta(3)-adrenergic receptor (beta(3)-AR) and oxidative stress in isoproterenol (ISO)-induced chronic heart failure (HF) rats.

Methods: Seven weight-matched normal adult rats (control), 18 ISO induced heart failure rats and 21 ISO induced heart failure rats treated with specific beta(3)-AR inhibitor, SR59230A for 6 weeks were included in this study. Echocardiography was performed at the end of the study and the myocardial levels of total superoxide dismutase (T-SOD) and lipid peroxidation (LPO) were measured by colorimetry, myocardial expression of beta(3)-AR was detected by reverse transcription-polymerase chain reaction (RT-PCR).

Result: Compared with control group, the cardiac function was significantly reduced and myocardial beta(3)-AR mRNA expression was significantly increased, LPO level was also significantly enhanced while T-SOD level was significantly reduced in ISO group and these changes could be significantly attenuated by treatment with SR59230A.

Conclusion: Our results showed that myocardial upregulation of beta(3)-AR is associated with increased oxidative stress in this model and beta(3)-AR inhibitor may be a new therapeutic agent for heart failure treatment.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gene Expression Regulation
  • Heart Failure / metabolism*
  • Heart Failure / physiopathology
  • Lipid Peroxidation
  • Male
  • Myocardium / metabolism*
  • Oxidative Stress*
  • Propanolamines / pharmacology
  • Rats
  • Rats, Wistar
  • Receptors, Adrenergic, beta-3 / metabolism*
  • Superoxide Dismutase / metabolism
  • Up-Regulation

Substances

  • 3-(2-ethylphenoxy)-1-(1,2,3,4-tetrahydronaphth-1-ylamino)-2-propanol oxalate
  • Propanolamines
  • Receptors, Adrenergic, beta-3
  • Superoxide Dismutase