TY - JOUR
T1 - Effect of Enalaprilat on nitric oxide activity in coronary artery disease
AU - Prasad, Abhiram
AU - Husain, Syed
AU - Quyyumi, Arshed A.
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1999/7/1
Y1 - 1999/7/1
N2 - Atherosclerosis is associated with vascular endothelial dysfunction and reduced nitric oxide (NO) activity. Enhancement of NO activity may have an antiatherogenic action. This study was performed to determine whether angiotensin-converting enzyme (ACE) inhibition improves peripheral vascular NO activity in patients with atherosclerosis. In the femoral circulation of 43 patients with atherosclerosis and 10 controls, we studied endothelium- dependent vasedilation with bradykinin and acetylcholine, and endothelium- independent vasodilation with sodium nitroprusside before and after enalaprilat. In 22 patients, we repeated these infusions in the presence of L-N(G) monomethyl arginine (L-NMMA). Doppler-femoral artery flow velocity was measured. Before ACE inhibition, acetylcholine responses were depressed in patients with atherosclerosis compared with controls (p = 0.03). Enalaprilat did not alter femoral vascular tone at rest or vasodilation with sodium nitroprusside, but potentiated bradykinin-mediated vasodilation in patients (p <0.001) and controls (p = 0.02). Acetylcholinemediated vasodilation was augmented only in patients (p <0.001), but not in control subjects. L-NMMA inhibited the potentiation by enalaprilat of acetylcholine and bradykinin responses. This study demonstrates that ACE inhibition selectively improves endothelial dysfunction in human atherosclerosis by enhancing NO activity. The antithrombotic and antiproliferative effects of NO may reduce adverse manifestations related to atherosclerosis during long-term therapy.
AB - Atherosclerosis is associated with vascular endothelial dysfunction and reduced nitric oxide (NO) activity. Enhancement of NO activity may have an antiatherogenic action. This study was performed to determine whether angiotensin-converting enzyme (ACE) inhibition improves peripheral vascular NO activity in patients with atherosclerosis. In the femoral circulation of 43 patients with atherosclerosis and 10 controls, we studied endothelium- dependent vasedilation with bradykinin and acetylcholine, and endothelium- independent vasodilation with sodium nitroprusside before and after enalaprilat. In 22 patients, we repeated these infusions in the presence of L-N(G) monomethyl arginine (L-NMMA). Doppler-femoral artery flow velocity was measured. Before ACE inhibition, acetylcholine responses were depressed in patients with atherosclerosis compared with controls (p = 0.03). Enalaprilat did not alter femoral vascular tone at rest or vasodilation with sodium nitroprusside, but potentiated bradykinin-mediated vasodilation in patients (p <0.001) and controls (p = 0.02). Acetylcholinemediated vasodilation was augmented only in patients (p <0.001), but not in control subjects. L-NMMA inhibited the potentiation by enalaprilat of acetylcholine and bradykinin responses. This study demonstrates that ACE inhibition selectively improves endothelial dysfunction in human atherosclerosis by enhancing NO activity. The antithrombotic and antiproliferative effects of NO may reduce adverse manifestations related to atherosclerosis during long-term therapy.
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U2 - 10.1016/S0002-9149(99)00182-4
DO - 10.1016/S0002-9149(99)00182-4
M3 - Article
C2 - 10404842
AN - SCOPUS:0033024364
SN - 0002-9149
VL - 84
SP - 1
EP - 6
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 1
ER -