Inhibitors of poly (ADP-ribose) synthetase protect rat cardiomyocytes against oxidant stress

Cardiovasc Res. 1999 Jan;41(1):126-34. doi: 10.1016/s0008-6363(98)00221-1.

Abstract

Objective: Inhibitors of poly (ADP-ribose) synthetase (PARS) activity reduce the infarct size caused by regional myocardial ischaemia and reperfusion in the rabbit and rat in vivo. The mechanism of action of these inhibitors is unclear. Here we investigate the effects of the PARS inhibitor 3-aminobenzamide (3-AB) on infarct size caused by ischaemia and reperfusion of the isolated, perfused heart of the rat. We also investigate the role of PARS in the hydrogen peroxide-mediated cell injury/necrosis in rat cardiac myoblasts.

Methods: Rat isolated hearts perfused at constant pressure (80 mmHg) were subjected to 35 min of regional ischaemia and 2 h of reperfusion. Infarct size was determined at the end of the experiment using nitro-blue tetrazolium. 3-AB (300 microM) or 3-aminobenzoic acid (3-ABA, 300 microM) were infused during the reperfusion period. Rat cardiac myoblasts (H9c2 cells) were preincubated with the PARS inhibitors, 3-AB. nicotinamide (Nic) or 1,5-dihydroxyisoquinoline (ISO) or the inactive analogues 3-ABA or nicotinic acid (NicA) prior to exposure with hydrogen peroxide (1 mM). Cell injury was assessed by measuring mitochondrial respiration and cell necrosis by measuring the release of LDH. PARS activity was determined by measuring the incorporation of NAD into nuclear proteins.

Results: Regional ischaemia and reperfusion of the isolated rat heart resulted in an infarct size of 54% which was reduced by 3-AB, but not by 3-ABA. Exposure of rat cardiac myoblasts to hydrogen peroxide caused an increase in PARS activity and cell injury/necrosis which was attenuated by pretreatment with the PARS inhibitors.

Conclusion: Inhibition of the activity of PARS attenuates the cell death associated with oxidant stress in rat cardiac myoblasts and heart.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminobenzoates / pharmacology
  • Animals
  • Benzamides / pharmacology*
  • Cell Death / drug effects
  • Cell Line
  • Enzyme Inhibitors / pharmacology*
  • Heart / drug effects*
  • Hydrogen Peroxide
  • Isoquinolines / pharmacology
  • Male
  • Myocardial Reperfusion Injury / prevention & control*
  • Niacin / pharmacology
  • Niacinamide / pharmacology
  • Oxidative Stress
  • Perfusion
  • Poly(ADP-ribose) Polymerase Inhibitors*
  • Poly(ADP-ribose) Polymerases / metabolism
  • Rats
  • Rats, Wistar
  • meta-Aminobenzoates

Substances

  • Aminobenzoates
  • Benzamides
  • Enzyme Inhibitors
  • Isoquinolines
  • Poly(ADP-ribose) Polymerase Inhibitors
  • meta-Aminobenzoates
  • Niacinamide
  • Niacin
  • 1,5-dihydroxyisoquinoline
  • 3-aminobenzamide
  • Hydrogen Peroxide
  • Poly(ADP-ribose) Polymerases
  • 3-aminobenzoic acid