E. Arbustini et al., MORPHOLOGIC CHANGES INDUCED BY ACETYLCHOLINE INFUSION IN NORMAL AND ATHEROSCLEROTIC CORONARY-ARTERIES, The American journal of cardiology, 71(16), 1993, pp. 1382-1390
Low doses of acetylcholine induce ''endothelium-dependent'' dilatation
in normal coronary arteries and constriction of diseased vessels. Thi
s study investigated morphologic changes induced by perfusion of norma
l and diseased coronary arteries with low and high doses of acetylchol
ine. Vessels were excised from a series of beating hearts explanted at
transplantation for idiopathic dilated cardiomyopathy and coronary ar
tery disease. Coronary arteries from other explanted hearts, perfused
with saline solution under similar condition were taken as controls. S
amples were studied using conventional histopathologic and immunohisto
chemical methods. Coronary arteries were grouped according to presence
or absence of histologically detectable structural modifications of a
ny type and extent. Low doses of acetylcholine induced changes in all
but 1 structurally diseased coronary artery, whereas no change was ind
uced in any but 1 histologically normal coronary artery. High doses of
acetylcholine induced contraction changes in both normal and diseased
vessels. Changes observed in the wall of the contracted vessels were:
(1) endothelial cell contraction with protruding nuclei and detachmen
t of their intercellular junctions with exposure of subjacent collagen
to flow, (2) contraction of plaque smooth muscle cells, (3) formation
of cushions protruding into vessel lumens causing blunt microchannels
. Contraction in both intimal and plaque cells occurred even in diseas
ed vessel segments with intimal denudation. These effects seemed to be
dose-dependent in structurally normal vessels because low doses of ac
etylcholine did not produce any morphologically detectable changes in
histologically normal coronary arteries, while low doses of acetylchol
ine induced similar reactions in vessels affected by both atherosclero
sis and subintimal fibrocellular thickening.