Estrogen-induced increases in coronary blood flow are antagonized by inhibitors of nitric oxide synthesis

被引:34
作者
Lang, U [1 ]
Baker, RS [1 ]
Clark, KE [1 ]
机构
[1] UNIV CINCINNATI,COLL MED,DEPT OBSTET & GYNECOL,PERINATAL RES INST,DIV MATERNAL FETAL MED,CINCINNATI,OH 45267
来源
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY | 1997年 / 74卷 / 02期
关键词
estradiol-17; beta; coronary; estrogens; cardiac output;
D O I
10.1016/S0301-2115(97)00104-8
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Estrogen receptors have been found in coronary arterial endothelial and vascular smooth muscle cells. Therefore the present study was designed to determine if estradiol-17 beta can increase coronary blood flow and if so whether the changes are mediated by nitric oxide. Study design: Five oophorectomized non-pregnant sheep were chronically instrumented to measure blood pressure, heart rate, cardiac output, left circumflex coronary blood flow and central venous pressure. Animals received estradiol-17 beta (1.0 mu g/kg) and cardiovascular responses were followed for 135 min. Results: Estradiol-17 beta (1.0 mu g/kg) increased left circumflex (coronary) blood flow 28+/-3%, cardiac output 15+/-1% and heart rate by 13+/-3%. Coronary vascular resistance decreased 231+/-5%, systemic vascular resistance decreased by 12+/-2% while blood pressure did not change significantly. Administration of the nitric oxide synthetase inhibitor L-nitroarginine methylester (L-NAME), had no effect on basal coronary blood Bow but completely reversed estradiol-17 beta induced increases in coronary blood flow. Conclusion: These results demonstrate that estrogen increases coronary blood flow in the non-pregnant sheep and that L-NAME, an inhibitor of nitric oxide, is able to reverse the estrogen induced flow changes. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:229 / 235
页数:7
相关论文
共 24 条
[1]   SECRETION OF STEROIDS FROM AUTOTRANSPLANTED OVARY IN EWE SPONTANEOUSLY AND IN RESPONSE TO SYSTEMIC GONADOTROPHIN [J].
BAIRD, DT ;
GODING, JR ;
ICHIKAWA, Y ;
MCCRACKEN, JA .
JOURNAL OF ENDOCRINOLOGY, 1968, 42 (02) :283-+
[2]  
BAKER RS, 1997, J SOC GYNECOL INVEST, V4, pA178
[4]  
BROBECK, 1979, PHYSL BASIS MED PRAC
[5]  
BUSH TL, 1990, ANN NY ACAD SCI, V592, P1002
[6]   PROGESTERONE AND ESTRADIOL IN PITUITARY, BRAIN AND UTERINE TISSUES OF SHEEP [J].
CHALLIS, JRG ;
LOUIS, TM ;
ROBINSON, JS ;
THORBURN, GD .
JOURNAL OF ENDOCRINOLOGY, 1976, 69 (03) :451-452
[7]   ESTROGEN-BINDING SITES IN ENDOTHELIAL CELL-CULTURES [J].
COLBURN, P ;
BUONASSISI, V .
SCIENCE, 1978, 201 (4358) :817-819
[8]   CARDIOVASCULAR PROTECTION BY ESTROGEN - A CALCIUM-ANTAGONIST EFFECT [J].
COLLINS, P ;
ROSANO, GMC ;
JIANG, CW ;
LINDSAY, D ;
SARREL, PM ;
POOLEWILSON, PA .
LANCET, 1993, 341 (8855) :1264-1265
[9]  
EASTERLING TR, 1990, CRITICAL CARE OBSTET, P78
[10]   LEFT-VENTRICULAR COMPLIANCE - MECHANISMS AND CLINICAL IMPLICATIONS [J].
GAASCH, WH ;
LEVINE, HJ ;
QUINONES, MA ;
ALEXANDER, JK .
AMERICAN JOURNAL OF CARDIOLOGY, 1976, 38 (05) :645-653