(-)-CGP 12177-induced increase of human atrial contraction through a putative third beta-adrenoceptor

被引:84
作者
Kaumann, AJ
机构
[1] Human Pharmacology Laboratory, Babraham Institute
关键词
human atrium; (-)-CGP 12177; positive inotropic effects; antagonism by (-)-bupranolol; beta(3)-adrenoceptors;
D O I
10.1111/j.1476-5381.1996.tb15159.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 The inotropic effects of (-)-4-(3-t-butylamino-2-hydroxypropoxy)benzimidazol-2-one ((-)-CGP 12177), an antagonist for beta(1)- and beta(2)-adrenoceptors as well as an agonist for beta(3)-adrenoceptors, were investigated on paced preparations of isolated right atrial appendages obtained from patients without advanced heart failure undergoing open heart surgery. 2 In the presence of (-)-propranolol (200 nM), (-)-CGP 12177 increased contractile force with a -log EC(50), M, of 7.3. The maximum effects of(-)-CGP 12177 amounted to 15% and 11% of the effects of (-)-isoprenaline (400 mu M) and of CaCl2 (6.75 mM) respectively. 3 (-)-Bupranolol 1 mu M, an antagonist with a pK(B) of similar to 7.5 for beta(3)-adrenoceptors, antagonized surmountably the positive inotropic effects of (-)-CGP 12177 (in the presence of 200 nM (-)propranolol) with an apparent pK(B) of 7.3. 4 The potent positive inotropic effects of (-)-CGP 12177 and their resistance to blockade by (-)propranolol but antagonism by (-)-bupranolol are consistent with the existence in human atrial myocardium of a minor third beta-adrenoceptor population, possibly related to beta(3)-adrenoceptors.
引用
收藏
页码:93 / 98
页数:6
相关论文
共 36 条
[11]  
GRANNEMAN JG, 1992, J PHARMACOL EXP THER, V261, P638
[12]   ANALYSIS OF HUMAN AND RODENT BETA(3)-ADRENERGIC RECEPTOR MESSENGER RIBONUCLEIC-ACIDS [J].
GRANNEMAN, JG ;
LAHNERS, KN .
ENDOCRINOLOGY, 1994, 135 (03) :1025-1031
[13]  
GRANNEMAN JG, 1993, MOL PHARMACOL, V44, P264
[14]   SELECTIVE BETA-1-ADRENOCEPTOR BLOCKADE ENHANCES POSITIVE INOTROPIC RESPONSES TO ENDOGENOUS CATECHOLAMINES MEDIATED THROUGH BETA-2-ADRENOCEPTORS IN HUMAN ATRIAL MYOCARDIUM [J].
HALL, JA ;
KAUMANN, AJ ;
BROWN, MJ .
CIRCULATION RESEARCH, 1990, 66 (06) :1610-1623
[15]   DIFFERENTIATION OF BETA-ADRENOCEPTORS IN RIGHT ATRIUM, DIAPHRAGM AND ADIPOSE-TISSUE OF RAT, USING STEREOISOMERS OF PROPRANOLOL, ALPRENOLOL, NIFENALOL AND PRACTOLOL [J].
HARMS, HH ;
ZAAGSMA, J ;
DEVENTE, J .
LIFE SCIENCES, 1977, 21 (01) :123-128
[16]   5-HYDROXYTRYPTAMINE CAUSES RATE-DEPENDENT ARRHYTHMIAS THROUGH 5-HT4 RECEPTORS IN HUMAN ATRIUM - FACILITATION BY CHRONIC BETA-ADRENOCEPTOR BLOCKADE [J].
KAUMANN, AJ ;
SANDERS, L .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1994, 349 (04) :331-337
[17]  
KAUMANN AJ, 1973, ACTA PHYSIOL LAT AM, V23, P235
[18]   BETA-ADRENOCEPTOR BLOCKING-AGENTS AS PARTIAL AGONISTS IN ISOLATED HEART-MUSCLE - DISSOCIATION OF STIMULATION AND BLOCKADE [J].
KAUMANN, AJ ;
BLINKS, JR .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1980, 311 (03) :237-248
[19]   A COMPARISON OF THE EFFECTS OF ADRENALINE AND NORADRENALINE ON HUMAN-HEART - THE ROLE OF BETA-1-ADRENOCEPTOR AND BETA-2-ADRENOCEPTOR IN THE STIMULATION OF ADENYLATE-CYCLASE AND CONTRACTILE-FORCE [J].
KAUMANN, AJ ;
HALL, JA ;
MURRAY, KJ ;
WELLS, FC ;
BROWN, MJ .
EUROPEAN HEART JOURNAL, 1989, 10 :29-37
[20]   IS THERE A 3RD HEART BETA-ADRENOCEPTOR [J].
KAUMANN, AJ .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1989, 10 (08) :316-320