Role of β-Adrenoceptors and L-Type Ca(2+)-Channels in the Mechanism of Reperfusion-Induced Heart Injury

Bull Exp Biol Med. 2016 May;161(1):20-3. doi: 10.1007/s10517-016-3335-0. Epub 2016 Jun 6.

Abstract

We studied the effects of β-adrenoceptor antagonists propranolol and nadolol and L-type Ca(2+)-channel blocker verapamil on cardiac reperfusion injury developed after 45-min coronary occlusion. The substances were injected intravenously 5 min before reperfusion. The results indicate that activation of β-adrenoceptors and opening of L-type Ca(2+)-channels promote the development of cardiac reperfusion injury, while blockage of β-adrenoceptors and/or L-type Ca(2+)-channels prevents reoxygenation-induced myocardial injury. Propranolol, nadolol, and verapamil can produce infraction-limiting effects after onset of ischemic heart injury.

Keywords: Ca2+ -channels; heart; postconditioning; reperfusion; β-adreneric receptors.

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Calcium Channels, L-Type / metabolism*
  • Male
  • Myocardial Reperfusion Injury / metabolism*
  • Myocardium / metabolism*
  • Nadolol / pharmacology
  • Propranolol / pharmacology
  • Rats
  • Receptors, Adrenergic, beta / metabolism*
  • Verapamil / pharmacology

Substances

  • Adrenergic beta-Antagonists
  • Calcium Channels, L-Type
  • Receptors, Adrenergic, beta
  • Nadolol
  • Propranolol
  • Verapamil