Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 1994;90:983-987

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Williams, J. K.
Right arrow Articles by Clarkson, T. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Williams, J. K.
Right arrow Articles by Clarkson, T. B.

Circulation, Vol 90, 983-987, Copyright © 1994 by American Heart Association


ARTICLES

Determinants of coronary artery reactivity in premenopausal female cynomolgus monkeys with diet-induced atherosclerosis

JK Williams, CA Shively and TB Clarkson
Department of Comparative Medicine, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, NC 27157-1040.

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.


This article has been cited by other articles:


Home page
J Am Coll CardiolHome page
C. L. Shufelt and C. N. Bairey Merz
Contraceptive hormone use and cardiovascular disease.
J. Am. Coll. Cardiol., January 20, 2009; 53(3): 221 - 231.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
C. Noel Bairey Merz, B. D. Johnson, B. L. Sharaf, V. Bittner, S. L. Berga, G. D. Braunstein, T. K. Hodgson, K. A. Matthews, C. J. Pepine, S. E. Reis, et al.
Hypoestrogenemia of hypothalamic origin and coronary artery disease in premenopausal women: a report from the NHLBI-sponsored WISE study
J. Am. Coll. Cardiol., February 5, 2003; 41(3): 413 - 419.
[Abstract] [Full Text] [PDF]


Home page
Psychosom. Med.Home page
C. A. Shively, J. K. Williams, K. Laber-Laird, and R. F. Anton
Depression and Coronary Artery Atherosclerosis and Reactivity in Female Cynomolgus Monkeys
Psychosom Med, September 1, 2002; 64(5): 699 - 706.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
A. Rozanski, J. A. Blumenthal, and J. Kaplan
Impact of Psychological Factors on the Pathogenesis of Cardiovascular Disease and Implications for Therapy
Circulation, April 27, 1999; 99(16): 2192 - 2217.
[Abstract] [Full Text] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
P. Zandberg, J. L. M. Peters, P. N. M. Demacker, M. J. Smit, E. G. de Reeder, and D. G. Meuleman
Tibolone Prevents Atherosclerotic Lesion Formation in Cholesterol-Fed, Ovariectomized Rabbits
Arterioscler. Thromb. Vasc. Biol., December 1, 1998; 18(12): 1844 - 1854.
[Abstract] [Full Text] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
H. T. Westerveld, J. E. R. van Lennep, H. W. O. R. van Lennep, A.-H. Liem, J. A. J. de Boo, Y. T. van der Schouw, and D. W. Erkelens
Apolipoprotein B and Coronary Artery Disease in Women : A Cross-sectional Study in Women Undergoing Their First Coronary Angiography
Arterioscler. Thromb. Vasc. Biol., July 1, 1998; 18(7): 1101 - 1107.
[Abstract] [Full Text] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
K. A. Roberts, M. M. Woo, and J. C. Rutledge
Nitric Oxide Mediates LDL Uptake in the Artery Wall in Response to High Concentrations of 17ß-Estradiol
Arterioscler. Thromb. Vasc. Biol., October 1, 1997; 17(10): 2123 - 2131.
[Abstract] [Full Text]


Home page
Reproductive SciencesHome page
R. F. Casper, N. J. MacLusky, C. Vanin, and T. J. Brown
Rationale for Estrogen With Interrupted Progestin as a New Low-Dose Hormonal Replacement Therapy
Reproductive Sciences, September 1, 1996; 3(5): 225 - 234.
[Abstract] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
J. K. Williams, M. S. Anthony, E. K. Honore, D. M. Herrington, T. M. Morgan, T. C. Register, and T. B. Clarkson
Regression of Atherosclerosis in Female Monkeys
Arterioscler. Thromb. Vasc. Biol., July 1, 1995; 15(7): 827 - 836.
[Abstract] [Full Text]