Protection of reperfused ischemic canine myocardium by CI-922, a new inhibitor of leukocyte activation

J Cardiovasc Pharmacol. 1988;12(5):608-14. doi: 10.1097/00005344-198811000-00016.

Abstract

There is increasing evidence that activated neutrophils cause myocardial injury during reperfusion of ischemic myocardium. This study was performed to assess the effect of Ci-922, an inhibitor of neutrophil activation, in a canine preparation of myocardial infarction. Dogs received 15-min infusions of CI-922 1 mg/kg or 5% dextrose beginning 30 min before occlusion of the left circumflex coronary artery. After occlusion for 90 min and reperfusion for 6 h, infarct size was determined by ex vivo perfusion of the left circumflex coronary artery with triphenyltetrazolium chloride. The percentage of the area at risk infarcted was: control, 42 +/- 5; and CI-922, 23 +/- 4 (p less than 0.05 vs. control). There were no significant inter-group differences in heart rate or mean arterial pressure, and CI-922 did not enhance collateral blood flow to the ischemic bed. After incubation with CI-922 (100 microM), production of superoxide anions by canine neutrophils activated by opsonized zymosam decreased from 3.5 +/- 0.2 to 2.0 +/- 0.4 nmol/10 min/10(6) cells (p less than 0.05). Thus, inhibition of neutrophil-mediated damage may explain the cardioprotective effect of CI-922.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Azoles / therapeutic use*
  • Coronary Circulation / drug effects
  • Dogs
  • Electrocardiography
  • Hemodynamics / drug effects
  • Indoles / therapeutic use*
  • Male
  • Myocardial Reperfusion Injury / prevention & control*
  • Myocardium / enzymology
  • Neutrophils / metabolism
  • Peroxidase / metabolism
  • Superoxides
  • Tetrazoles / therapeutic use*

Substances

  • Azoles
  • Indoles
  • Tetrazoles
  • Superoxides
  • CI 922
  • Peroxidase