Gender-specific differences in the effects of testosterone and estrogen on the development of atherosclerosis in rabbits

被引:105
作者
Bruck, B
Brehme, U
Gugel, N
Hanke, S
Finking, G
Lutz, C
Benda, N
Schmahl, FW
Haasis, R
Hanke, H
机构
[1] UNIV TUBINGEN,DEPT MED BIOMETRY,D-72074 TUBINGEN,GERMANY
[2] UNIV TUBINGEN,DEPT INTERNAL MED,DIV CARDIOL,D-72074 TUBINGEN,GERMANY
[3] UNIV ULM,DEPT INTERNAL MED,DIV CARDIOL,D-89069 ULM,GERMANY
关键词
atherosclerosis; estrogen; testosterone; rabbits;
D O I
10.1161/01.ATV.17.10.2192
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
The aim of the present study was to investigate whether there are gender-specific differences in the effects of testosterone and estrogen on the process of atherogenesis. Thirty-two castrated male and 32 ovariectomized female rabbits were separated into 4 study groups of 8 males and 8 females each and received postoperatively a 0.5% cholesterol diet for 12 weeks. During this period either no hormones, estradiol (1 mg/kg body wt/week), testosterone (25 mg/kg body wt/week IMM), or estrogen combined with testosterone in above dosages were administered. Computerized morphometric analysis of the intimal thickening in the proximal aortic arch showed a significant inhibitory effect of estrogen in female and of testosterone in male animals (P<.05). In the group with combined treatment, the plaque size in both sexes was smaller than in the animals of the control group (P<.05). These differences were independent of changes in plasma lipid parameters. The incorporation of 5'-bromo-2'-deoxyuridine, associated with cell proliferation, into cells of the neointima was not significantly affected by the different hormone application regimens in males. In females, the incorporation rate was significantly lowered in the estrogen treated group compared with the control group (P<.05). Due to the observed differences in the sex specific atheroprotective effects of testosterone and estrogen, these data suggest that complex hormone interactions, which are independent of changes in plasma lipids, may play an important role in the process of atherogenesis.
引用
收藏
页码:2192 / 2199
页数:8
相关论文
共 47 条
[1]
INHIBITION OF CORONARY-ARTERY ATHEROSCLEROSIS BY 17-BETA ESTRADIOL IN OVARIECTOMIZED MONKEYS - LACK OF AN EFFECT OF ADDED PROGESTERONE [J].
ADAMS, MR ;
KAPLAN, JR ;
MANUCK, SB ;
KORITNIK, DR ;
PARKS, JS ;
WOLFE, MS ;
CLARKSON, TB .
ARTERIOSCLEROSIS, 1990, 10 (06) :1051-1057
[2]
ADAMS MR, 1995, ARTERIOSCLER THROMB, V15, P592
[3]
ANITSCHKOW N, 1914, PATHOLOGE, V59
[4]
[Anonymous], 1970, JAMA, V214, P1303
[5]
ESTROGEN AND CORONARY HEART-DISEASE IN WOMEN [J].
BARRETTCONNOR, E ;
BUSH, TL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1991, 265 (14) :1861-1867
[6]
THE RELATIONSHIP BETWEEN THE DEGREE OF DIETARY-INDUCED HYPERCHOLESTEROLEMIA IN THE RABBIT AND ATHEROSCLEROTIC LESION FORMATION [J].
BOCAN, TMA ;
MUELLER, SB ;
MAZUR, MJ ;
UHLENDORF, PD ;
BROWN, EQ ;
KIEFT, KA .
ATHEROSCLEROSIS, 1993, 102 (01) :9-22
[7]
CELLULAR PATHOLOGY OF PROGRESSIVE ATHEROSCLEROSIS IN THE WHHL RABBIT - AN ANIMAL-MODEL OF FAMILIAL HYPERCHOLESTEROLEMIA [J].
BUJA, LM ;
KITA, T ;
GOLDSTEIN, JL ;
WATANABE, Y ;
BROWN, MS .
ARTERIOSCLEROSIS, 1983, 3 (01) :87-101
[8]
NONCONTRACEPTIVE ESTROGEN USE AND CARDIOVASCULAR-DISEASE [J].
BUSH, TL ;
BARRETTCONNOR, E .
EPIDEMIOLOGIC REVIEWS, 1985, 7 :80-104
[9]
CLARKSON TB, 1994, FERTIL STERIL, V62, pS147
[10]
17-BETA-ESTRADIOL ATTENUATES ACETYLCHOLINE-INDUCED CORONARY ARTERIAL CONSTRICTION IN WOMEN BUT NOT MEN WITH CORONARY HEART-DISEASE [J].
COLLINS, P ;
ROSANO, GMC ;
SARREL, PM ;
ULRICH, L ;
ADAMOPOULOS, S ;
BEALE, CM ;
MCNEILL, JG ;
POOLEWILSON, PA .
CIRCULATION, 1995, 92 (01) :24-30