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Cardioprotective and endothelial protective effects of [Ala‐IL8] 77 in a rabbit model of myocardial ischaemia and reperfusion
Author(s) -
Lefer Allan M.,
III Gerald Johnson,
Ma Xinliang,
Tsao Phillip S.,
Thomas G. Roger
Publication year - 1991
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.1991.tb12316.x
Subject(s) - medicine , endothelial dysfunction , ischemia , endothelium , interleukin 8 , myeloperoxidase , reperfusion injury , vasodilation , coronary occlusion , cardiology , inflammation
1 We studied the effects of a form of interleukin‐8 (i.e., [Ala‐IL8] 77 ) on endothelial dysfunction and myocardial injury in rabbits. Pentobarbitone‐anaesthetized rabbits were subjected to 1.5 h occlusion of the marginal coronary artery and 3.5 h reperfusion. [Ala‐IL8] 77 (50 μg or its vehicle) was given i.v. as a bolus 10 min prior to reperfusion. [Ala‐IL8] 77 was also studied in isolated perfused hearts of rabbits. 2 Myocardial ischaemia plus reperfusion in untreated rabbits produced severe endothelial dysfunction and myocardial injury, including marked myocardial necrosis, elevated cardiac myeloperoxidase (MPO) activity in ischaemic cardiac tissue, and loss of response of marginal coronary rings to the endothelium‐dependent vasodilators, acetylchloline (ACh) and A23187. 3 Administration of [Ala‐IL8] 77 10 min prior to reperfusion resulted in significant protective effects in post‐ischaemic reperfusion. Compared with untreated rabbits, [Ala‐IL8] 77 caused a reduced necrotic zone ( P < 0.01), lower MPO activity in the necrotic zone ( P < 0.05), and significantly preserved vasorelaxant responses of marginal coronary artery rings to endothelium‐dependent vasodilators, ACh ( P < 0.001) and A23187( P < 0.001). 4 These results indicate that myocardial ischaemia and reperfusion result in a severe endothelial dysfunction and myocardial injury which involved the interaction of neutrophils and endothelial cells. However, [Ala‐IL8] 77 did not appear to exert a direct endothelial protective effect in the absence of neutrophils in rabbit isolated perfused hearts. 5 Inhibition of neutrophil accumulation in the myocardium, perhaps by prevention of endothelial dysfunction resulting from [Ala‐IL8] 77 , leads to significant protective effects in ischaemia and reperfusion in rabbits.