Upregulation of β3-adrenergic receptor expression in the atrium of rats with chronic heart failure

J Cardiovasc Pharmacol Ther. 2013 Mar;18(2):133-7. doi: 10.1177/1074248412460123. Epub 2012 Sep 24.

Abstract

Objectives: To investigate the expression of β(3)-adrenergic receptor (β(3)-AR) in the atrium of rats with chronic heart failure (CHF).

Methods: The heart failure rat model was established by aortic constriction. Thirty-six male Wistar rats were divided into Sham group (n = 10) and heart failure model group (n = 26), which were further divided into CHF control (CHF group) and BRL group. The rats in the BRL group were treated with a selective β(3)-AR agonist, BRL-37344 (4.0 nmol/kg, twice weekly) for 4 weeks.

Results: In the BRL group, the left ventricular end-systolic pressure (83.21 ± 13.0 vs 101.50 ± 12.12 mm Hg) and the absolute values of the maximal rate of rise and fall of left ventricular pressure ([±dP/dtmax] 2.81 ± 0.04 vs 0.35 ± 0.04 and -2.72 ± 0.06 vs -3.33 ± 0.06) were lower than in the CHF group (P < .01). The left atrial mass index (LAMI) in the BRL group (0.4132 ± 0.0306) was higher than that in the CHF (0.3212 ± 0.0136) or Sham group (0.2683 ± 0.0145; P < .01). The levels of the left atrial β(3)-AR messenger RNA (mRNA) expression in the BRL group (0.932 ± 0.055) was higher than that in the CHF (0.706 ± 0.043) or Sham group (0.310 ± 0.020; P < .01). In all animals, there was a positive correlation between the level of β(3)-AR mRNA expression and the left or right atrial mass index (correlation coefficient ranged from 0.744 to 0.937).

Conclusion: There is a significant increase in the β(3)-AR mRNA expression in the atrium of rats with heart failure. The level of β(3)-AR mRNA expression was associated with the AMI and was enhanced by a selective β(3)-AR agonist, BRL-37344.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chronic Disease
  • Heart Atria / metabolism*
  • Heart Atria / pathology
  • Heart Failure / metabolism*
  • Heart Failure / pathology
  • Male
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Wistar
  • Receptors, Adrenergic, beta-3 / biosynthesis*
  • Receptors, Adrenergic, beta-3 / genetics
  • Up-Regulation* / genetics

Substances

  • RNA, Messenger
  • Receptors, Adrenergic, beta-3