Antibody to CD-18 exerts endothelial and cardiac protective effects in myocardial ischemia and reperfusion

306Citations
Citations of this article
38Readers
Mendeley users who have this article in their library.

Abstract

We studied the effects of MAbR15.7, an antibody directed against the common β-chain (CD-18) of a family of neutrophil adherence glycoproteins, on endothelial dysfunction and myocardial injury in a model of myocardial ischemia and reperfusion in cats. Pentobarbital-anesthetized cats were subjected to 1.5 h occlusion of the left anterior descending coronary artery (LAD) and 4.5 h of reperfusion. MI + R resulted in severe myocardial injury and endothelial dysfunction, including signifiant elevation of plasma creatine kinase (CK) activity, marked myocardial necrosis, high cardiac myeloperoxidase (MPO) activity in ischemic cardiac tissue, and loss of response of LAD coronary rings to the endothelium-dependent vasodilators, acetylcholine (ACh) and A-23187. In contrast, MAbR15.7-treated arts exhibited a lower plasma CK activity at every time point observed after 2 h, a reduced area of cardiac necrosis (2±1 vs. 30.8±2.5% of area-at-risk, P < 0.001), lower MPO activity in the ischemic region (P < 0.01), and significantly preserved vasorelaxant responses of LAD coronary rings to endothelium-dependent vasodilators, ACh (P < 0.001), and A-23187 (P < 0.001). These results indicate that myocardial ischemia and reperfusion induces significant myocardial injury and endothelial dysfunction in the cat involving a CD18-dependent neutrophil adherence mechanism. Inhibition of neutrophil adherence to the endothelium exerts significant protective effects in this model of reperfusion injury.

Cite

CITATION STYLE

APA

Ma, X. L., Tsao, P. S., & Lefer, A. M. (1991). Antibody to CD-18 exerts endothelial and cardiac protective effects in myocardial ischemia and reperfusion. Journal of Clinical Investigation, 88(4), 1237–1243. https://doi.org/10.1172/JCI115427

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free