The effect of valsartan on the angiotensin II pressor response in healthy normotensive male subjects

被引:18
作者
Morgan, JM
Palmisano, M
Piraino, A
Hirschhorn, W
Spencer, S
Prasad, PP
Ortiz, M
Lloyd, P
机构
[1] ALLEGHENY UNIV HLTH SCI,DEPT PHARMACOL,PHILADELPHIA,PA 19102
[2] MED COLL PENN & HAHNEMANN UNIV,PHILADELPHIA,PA
[3] DIV CIBA GEIGY LTD,CIBA PHARMA,SUMMIT,NJ
关键词
D O I
10.1016/S0009-9236(97)90180-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: Valsartan is an oral antagonist of angiotensin II that competes with angiotensin LI for the AT(1)-receptor and is being developed as an antihypertensive agent. This study assessed the ability of 80 mg valsartan to inhibit the pressor effect of exogenous angiotensin II in healthy normotensive men, fist after a single dose and then after multiple doses once daily for 7 days. Methods: This was a single-center, double-blind, placebo-controlled, randomized crossover study. Six healthy men underwent angiotensin II challenges to determine a suitable dose required to increase their systolic blood pressure by approximately 30 mm Hg. Each subject then received an 80 mg dose of valsartan or matching placebo. The inhibition of the angiotensin II presser effect was determined by the systolic blood pressure response to repeated angiotensin II challenges at multiple time points. Results: Systolic blood pressure responses to angiotensin II challenges after single and multiple doses of valsartan were significantly lower than placebo, indicating that valsartan blocked the blood pressure response to angiotensin II. The maximum blocking effect was observed within 2 to 3 hours. Mean data suggested that differences in effect between valsartan and placebo were similar after both single and multiple doses and persisted up to 24 hours after administration. The angiotensin II blocking effect was maintained up to this time, despite low plasma valsartan levels and minimal accumulation after multiple doses. Conclusion: Valsartan, 80 mg, is a potent angiotensin II antagonist with a rapid onset of action and persistent angiotensin II inhibition up to 24 hours. There is no attenuation of this effect after multiple doses.
引用
收藏
页码:35 / 44
页数:10
相关论文
共 22 条
[1]  
BRUNNER HR, 1990, ANGIOTENSIN CONVERTI, P732
[2]  
BRUNNER LM, 1993, 93027 CPD
[3]   NONINVASIVE BLOOD-PRESSURE MONITORING AT THE FINGER FOR STUDYING SHORT LASTING PRESSOR-RESPONSES IN MAN [J].
CHRISTEN, Y ;
WAEBER, B ;
NUSSBERGER, J ;
BRUNNER, HR .
JOURNAL OF CLINICAL PHARMACOLOGY, 1990, 30 (08) :711-714
[4]  
CHRISTEN Y, 1991, AM J HYPERTENS, V4
[5]   PHARMACOLOGICAL PROFILE OF VALSARTAN - A POTENT, ORALLY-ACTIVE, NONPEPTIDE ANTAGONIST OF THE ANGIOTENSIN-II AT1-RECEPTOR SUBTYPE [J].
CRISCIONE, L ;
DEGASPARO, M ;
BUHLMAYER, P ;
WHITEBREAD, S ;
RAMJOUE, HPR ;
WOOD, J .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 110 (02) :761-771
[6]   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
[7]   ANGIOTENSIN-II RECEPTOR BLOCKADE - AN INNOVATIVE APPROACH TO CARDIOVASCULAR PHARMACOTHERAPY [J].
EBERHARDT, RT ;
KEVAK, RM ;
KANG, PM ;
FRISHMAN, WH .
JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 33 (11) :1023-1038
[8]  
FLESCH G, 1993, EUR J DRUG METAB S1, V18, P117
[9]  
HILDITCH A, 1995, J PHARMACOL EXP THER, V272, P750
[10]   UNDERSTANDING THE DOSE-EFFECT RELATIONSHIP - CLINICAL-APPLICATION OF PHARMACOKINETIC-PHARMACODYNAMIC MODELS [J].
HOLFORD, NHG ;
SHEINER, LB .
CLINICAL PHARMACOKINETICS, 1981, 6 (06) :429-453