ROLE OF ENDOGENOUS ENDOTHELIN IN NORMAL HEMODYNAMIC STATUS OF ANESTHETIZED DOGS

被引:53
|
作者
TEERLINK, JR
CARTEAUX, JP
SPRECHER, U
LOFFLER, BM
CLOZEL, M
CLOZEL, JP
机构
[1] F HOFFMANN LA ROCHE & CO LTD, PRECLIN RES, DIV PHARMA, CH-4002 BASEL, SWITZERLAND
[2] CHU NANCY, SERV CHIRURG CARDIAQUE & TRANSPLANTAT CARDIOTHORA, F-54500 VANDOEUVRE LES NANCY, FRANCE
[3] UNIV CALIF SAN FRANCISCO, MED CTR, DEPT MED, DIV CARDIOL, SAN FRANCISCO, CA 94143 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1995年 / 268卷 / 01期
关键词
CORONARY CIRCULATION; SARAFOTOXIN S6C; BOSENTAN; HYPERTENSION; MYOCARDIAL ISCHEMIA;
D O I
10.1152/ajpheart.1995.268.1.H432
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Endothelin (ET) is a potent vasoconstrictor that may be involved in a number of cardiovascular disorders, although its role in normal hemodynamics remains unclear. Twenty-two anesthetized open-chest dogs were instrumented for measurement of systemic and pulmonary hemodynamics, cardiac output, coronary blood flow, and cardiac contractility. Big ET induced peripheral and coronary vasoconstriction, which occurred before significant elevations in plasma ET and which was nearly completely blocked by bosentan, a new nonpeptidic mixed (ET(A) and ET(B)) ET receptor antagonist. Bosentan also prevented the peripheral dilatation caused by the specific ET(B) receptor agonist, sarafotoxin S6c, but did not prevent the peripheral vasoconstriction induced by angiotensin II. Bosentan alone had no significant hemodynamic effect in the normal anesthetized dog, although it did induce a reactive increase in the plasma level of ET-1 and ET-3. This study demonstrates that, despite blocking both ET(A) and ET(B) receptors, bosentan alone had no hemodynamic effect, suggesting that ET does not play a major role in the normal hemodynamic status of anesthetized dogs.
引用
收藏
页码:H432 / H440
页数:9
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