Sex differences in the effects of 17 beta-estradiol on vascular adrenergic responses

被引:10
作者
GarciaVillalon, AL
Buchholz, JN
Krause, DN
Duckles, SP
机构
[1] UNIV CALIF IRVINE,COLL MED,DEPT PHARMACOL,IRVINE,CA 92717
[2] UNIV AUTONOMA MADRID,FAC MED,DEPT FISIOL,E-28029 MADRID,SPAIN
[3] LOMA LINDA UNIV,SCH MED,DEPT PHARMACOL,LOMA LINDA,CA 92350
关键词
tail artery; rat; adrenergic nerve stimulation; noradrenaline release; gonadectomy;
D O I
10.1016/S0014-2999(96)00565-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The in vitro effects of 17 beta-estradiol on vascular responses to adrenergic nerve stimulation were studied in perfused tail arteries from age-matched male and female rats. Nerve stimulation resulted in vasoconstriction that was greater in male arteries. Addition of 17 beta-estradiol (3 X 10(-5) M) reduced the vasoconstrictor responses in both male and female arteries, but the reduction was significantly greater in the females. Gonadectomy of the animals for 1 month prior to the experiment did not alter the in vitro responses to 17 beta-estradiol in either males or females. 17 beta-Estradiol (10(-6)-3 X 10(-5) M) also relaxed perfused tail arteries precontracted with KCl (50 mM); however the relaxation was not different between males and females, either intact or gonadectomized. Stimulation-evoked release of noradrenaline from adrenergic nerves of perfused tail arteries was measured, but no differences were found between males and females, nor was release modified by in vitro exposure to 17 beta-estradiol (10(-5) M). These results suggest that 17 beta-estradiol acts directly on postjunctional mechanisms to relax tail arteries of either sex. The effect of the hormone on arteries constricted by adrenergic nerve stimulation, however, is greater in females compared to males.
引用
收藏
页码:339 / 345
页数:7
相关论文
共 19 条
[1]  
ALTURA BM, 1975, J PHARMACOL EXP THER, V193, P403
[2]   REGIONAL SEX-DIFFERENCES IN CELL NUCLEAR ESTROGEN-BINDING CAPACITY IN THE RAT HYPOTHALAMUS AND PREOPTIC AREA [J].
BROWN, TJ ;
HOCHBERG, RB ;
ZIELINSKI, JE ;
MACLUSKY, NJ .
ENDOCRINOLOGY, 1988, 123 (04) :1761-1770
[3]   RACE, SEX AND OCCLUSIVE CEREBROVASCULAR-DISEASE - A REVIEW [J].
CAPLAN, LR ;
GORELICK, PB ;
HIER, DB .
STROKE, 1986, 17 (04) :648-655
[4]   CHRONIC ESTROGEN ALTERS CONTRACTILE RESPONSIVENESS TO ANGIOTENSIN-II AND NOREPINEPHRINE IN FEMALE RAT AORTA [J].
CHENG, DY ;
GRUETTER, CA .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 215 (2-3) :171-176
[5]   INCREASED VASCULAR CATECHOLAMINE SENSITIVITY AND ALPHA-ADRENERGIC RECEPTOR AFFINITY IN FEMALE AND ESTROGEN-TREATED MALE-RATS [J].
COLUCCI, WS ;
GIMBRONE, MA ;
MCLAUGHLIN, MK ;
HALPERN, W ;
ALEXANDER, RW .
CIRCULATION RESEARCH, 1982, 50 (06) :805-811
[6]   SEX-ROLES, SMOKING, AND SMOKING CESSATION [J].
DICKEN, C .
JOURNAL OF HEALTH AND SOCIAL BEHAVIOR, 1978, 19 (03) :324-334
[7]  
GISCLARD V, 1987, J PHARMACOL EXP THER, V240, P466
[8]  
GUYTON AC, 1995, TXB MED PHYSL, P1003
[9]   ENDOTHELIUM-INDEPENDENT RELAXATION OF RABBIT CORONARY-ARTERY BY 17-BETA-ESTRADIOL INVITRO [J].
JIANG, CW ;
SARREL, PM ;
LINDSAY, DC ;
POOLEWILSON, PA ;
COLLINS, P .
BRITISH JOURNAL OF PHARMACOLOGY, 1991, 104 (04) :1033-1037
[10]   PATTERNS OF CORONARY HEART-DISEASE MORBIDITY AND MORTALITY IN THE SEXES - A 26-YEAR FOLLOW-UP OF THE FRAMINGHAM POPULATION [J].
LERNER, DJ ;
KANNEL, WB .
AMERICAN HEART JOURNAL, 1986, 111 (02) :383-390