Circulation, Vol 90, 983-987, Copyright © 1994 by American Heart Association
JK Williams, CA Shively and TB Clarkson
BACKGROUND: The purpose of this study was to identify determinants of
coronary artery reactivity among premenopausal female monkeys. Estrogen
replacement therapy in postmenopausal females modulates reactivity of
atherosclerotic coronary arteries. However, no studies have evaluated the
factors that modulate coronary artery reactivity among premenopausal
females. METHODS AND RESULTS: Twenty-five adult premenopausal female
monkeys were fed an atherogenic diet for 32 months. During this time,
monkeys were housed in small social groups and determined to be socially
dominant (associated with normal ovarian function) or subordinate
(associated with impaired ovarian function). After 32 months, coronary
artery vasomotor responses to intracoronary acetylcholine, nitroglycerin,
and serotonin were assessed by computer- assisted quantitative coronary
angiography. Coronary arteries of dominant monkeys dilated (+9 +/- 2%),
whereas those of subordinate monkeys constricted (-6 +/- 2%) in response to
acetylcholine (P < .05). There was no effect of social status on
vascular response to nitroglycerin or serotonin (P > .10). Vascular
responses to acetylcholine were independent of social status effects on
plasma lipids, blood pressure, and atherosclerosis extent. The correlation
between acetylcholine responses and plasma estradiol concentration measured
on the day of angiography was r = .7 (P = < .01). Furthermore, dilation
occurred only if plasma estradiol concentrations were greater than 60
pg/mL. CONCLUSIONS: Psychosocial factors and endogenous estrogen production
are important modulators of acetylcholine-mediated dilation of
atherosclerotic coronary arteries among premenopausal female monkeys.
ARTICLES
Determinants of coronary artery reactivity in premenopausal female cynomolgus monkeys with diet-induced atherosclerosis
Department of Comparative Medicine, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, NC 27157-1040.
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