Comparison between angiotensin receptor antagonism and converting enzyme inhibition in heart failure -: Differential acute effects according to the renin-angiotensin system activation

被引:5
作者
Su, J
Barbe, F
Houël, R
Guyene, TT
Crozatier, B
Hittinger, L
机构
[1] Hop Leon Bernard, INSERM U400, F-94456 Limeil Brevannes, France
[2] Hop Broussais, Unite 367, F-75005 Paris, France
关键词
congestive heart failure; conscious dog; angiotensin II receptor antagonist; angiotensin converting enzyme inhibitor; vascular tone;
D O I
10.1007/s003950050135
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study was designed to assess the influence of the activation status of the renin angiotensin system (RAS) on the hemodynamic effects of EXP 3174 (an angiotensin AT1 receptor antagonist) and enalaprilat (an angiotensin converting enzyme inhibitor) in tachycardia-induced heart failure. Thirteen dogs were chronically instrumented to measure left ventricular (LV) pressure, its first time derivative (LV dP/dt), atrial and aortic pressures, and cardiac output. EXP 3174 (0.1 mg/kg, iv) or enalaprilat (I mg/kg, iv) were administered in conscious does with heart failure induced by right ventricular pacing (250 beats/min, 3 weeks). EXP 3174 and enalaprilat produced significant vasodilation but tho effects of EXP 3174 on mean aortic pressure (MAP!, cardiac output, and total peripheral resistance (TPR) were only 50 % of those produced by enalaprilat. When does were grouped according to their baseline plasma renin activity (PRA) values, in dogs with normal PRA (0.5 +/- 0.1 ng/ml/h) EXP 3174 did not produce significant change in MAP and TPR? while enalaprilat decreased significantly MAP and TPR. In contrast, in dogs with high PRA (6.7 +/- 3.2 ng/ml/h), EXP 3174 produced significant reductions in MAP and TPR, which were similar to those produced by enalaprilat. Thus, in conscious does with heart failure, enalaprilat is effective whether the RAS is activated or not. In contrast, EXP 3174 is effective only when the RAS is activated. These results may help in the choice of inhibitors of the RAS in heart failure.
引用
收藏
页码:128 / 135
页数:8
相关论文
共 36 条
[1]   Bradykinin pathway is involved in acute hemodynamic effects of enalaprilat in dogs with heart failure [J].
Barbe, F ;
Su, JB ;
Guyene, TT ;
Crozatier, B ;
Menard, J ;
Hittinger, L .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 270 (06) :H1985-H1992
[2]   RENIN RELATIONSHIPS IN CONGESTIVE CARDIAC FAILURE, TREATED AND UNTREATED [J].
BROWN, JJ ;
DAVIES, DL ;
JOHNSON, VW ;
LEVER, AF ;
ROBERTSON, JI .
AMERICAN HEART JOURNAL, 1970, 80 (03) :329-+
[3]  
CASCIERI D, 1984, MOL PHARMACOL, V10, P13
[4]   LOSARTAN IN HEART-FAILURE - HEMODYNAMIC-EFFECTS AND TOLERABILITY [J].
CROZIER, I ;
IKRAM, H ;
AWAN, N ;
CLELAND, J ;
STEPHEN, N ;
DICKSTEIN, K ;
FREY, M ;
YOUNG, J ;
KLINGER, G ;
MAKRIS, L ;
RUCINSKA, E .
CIRCULATION, 1995, 91 (03) :691-697
[5]   ROLE OF RENIN-ANGIOTENSIN SYSTEM IN SYSTEMIC VASOCONSTRICTION OF CHRONIC CONGESTIVE HEART-FAILURE [J].
CURTISS, C ;
COHN, JN ;
VROBEL, T ;
FRANCIOSA, JA .
CIRCULATION, 1978, 58 (05) :763-770
[6]  
DZAU VJ, 1981, CIRCULATION, V63, P645, DOI 10.1161/01.CIR.63.3.645
[7]   ANGIOTENSIN-II RECEPTOR ANTAGONISM IN OVINE HEART-FAILURE - ACUTE HEMODYNAMIC, HORMONAL, AND RENAL EFFECTS [J].
FITZPATRICK, MA ;
RADEMAKER, MT ;
CHARLES, CJ ;
YANDLE, TG ;
ESPINER, EA ;
IKRAM, H .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (01) :H250-H256
[8]   COMPARISON OF NEUROENDOCRINE ACTIVATION IN PATIENTS WITH LEFT-VENTRICULAR DYSFUNCTION WITH AND WITHOUT CONGESTIVE-HEART-FAILURE - A SUBSTUDY OF THE STUDIES OF LEFT-VENTRICULAR DYSFUNCTION (SOLVD) [J].
FRANCIS, GS ;
BENEDICT, C ;
JOHNSTONE, DE ;
KIRLIN, PC ;
NICKLAS, J ;
LIANG, CS ;
KUBO, SH ;
RUDINTORETSKY, E ;
YUSUF, S .
CIRCULATION, 1990, 82 (05) :1724-1729
[9]   HEMODYNAMIC AND NEUROHORMONAL EFFECTS OF THE ANGIOTENSIN-II ANTAGONIST LOSARTAN IN PATIENTS WITH CONGESTIVE-HEART-FAILURE [J].
GOTTLIEB, SS ;
DICKSTEIN, K ;
FLECK, E ;
KOSTIS, J ;
LEVINE, TB ;
LEJEMTEL, T ;
DEKOCK, M .
CIRCULATION, 1993, 88 (04) :1602-1609
[10]  
GROSS DM, 1981, J PHARMACOL EXP THER, V216, P552