α1-Adrenoceptor antagonist properties of CGP 12177A and other β-adrenoceptor ligands:: evidence against β3- or atypical β-adrenoceptors in rat aorta

被引:41
作者
Brahmadevara, N [1 ]
Shaw, AM [1 ]
Macdonald, A [1 ]
机构
[1] Glasgow Caledonian Univ, Sch Life Sci, Dept Biol & Biomed Sci, Glasgow G4 0BA, Lanark, Scotland
关键词
beta-adrenoceptors; beta(3)-adrenoceptors; low affinity state of beta(1)-adrenoceptors; atypical beta-adrenoceptors; rat aorta; CGP; 12177A; nonconventional partial agonists; alpha; 1-adrenoceptors;
D O I
10.1038/sj.bjp.0705840
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 The alpha(1)-adrenoceptor antagonist properties of the beta-adrenoceptor nonconventional partial agonist, CGP 12177A, was investigated in functional assays in rat aorta and in radioligand binding assays in rat cerebral cortical membranes. In addition, binding affinities of other beta-adrenoceptor ligands were measured to investigate any correlation between alpha(1)-adrenoceptor affinity and relaxant potency in phenylephrine-constricted rings. 2 In functional studies, CGP 12177A produced parallel rightward shifts of the phenylephrine CRC with no reduction in the maximum responses. Schild regression analysis gave a straight line with a slope of 0.95 (95% CL: 0.87-1.04), suggesting reversible competitive antagonism, and gave a pK(B) value of 5.26. In contrast, CGP 12177A (less than or equal to300 muM) had no effect on contraction induced by the thromboxane-mimetic, U46619. 3 In binding studies, CGP 12177A competed monophasically with [H-3]prazosin binding ( Hill slope, 0.95, 95% CL: 0.76-1.13), giving a pK(i) value of 5.48, in good agreement with the pK(B) from functional studies. 4 Competition experiments with various other beta-adrenoceptor ligands showed that they all displaced [H-3] prazosin in a manner consistent with one-site competition. pK(i) values were as follows: SR 59230A, 6.25; cyanopindolol, 6.33; bupranolol, 6.35; alprenolol, 5.90; propranolol, 5.80; BRL 37344, 5.50; ICI 118551, 5.55; CGP 20712A, 5.26. The pK(i) values correlated well with the pEC(50) values for relaxation of phenylephrine-constricted rat aorta obtained previously (r(2) = 0.984, P < 0.0001). 5 In conclusion, relaxant effects of CGP 12177A and other beta-adrenoceptor ligands in phenylephrine-constricted rat aorta can be attributed to alpha(1)-adrenoceptor blockade and are unrelated to effects at beta(3)-adrenoceptors or atypical beta-adrenoceptors. British Journal of Pharmacology (2004).
引用
收藏
页码:781 / 787
页数:7
相关论文
共 38 条
[1]   ATYPICAL BETA-ADRENOCEPTOR ON BROWN ADIPOCYTES AS TARGET FOR ANTI-OBESITY DRUGS [J].
ARCH, JRS ;
AINSWORTH, AT ;
CAWTHORNE, MA ;
PIERCY, V ;
SENNITT, MV ;
THODY, VE ;
WILSON, C ;
WILSON, S .
NATURE, 1984, 309 (5964) :163-165
[2]   SOME QUANTITATIVE USES OF DRUG ANTAGONISTS [J].
ARUNLAKSHANA, O ;
SCHILD, HO .
BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1959, 14 (01) :48-58
[3]   DISODIUM (R,R)-5-[2-[[2-(3-CHLOROPHENYL)-2-HYDROXYETHYL]AMINO]PROPYL]-1,3-BENZODIOXOLE-2,2-DICARBOXYLATE (CL 316,243) - A POTENT BETA-ADRENERGIC AGONIST VIRTUALLY SPECIFIC FOR BETA-3 RECEPTORS - A PROMISING ANTIDIABETIC AND ANTIOBESITY AGENT [J].
BLOOM, JD ;
DUTIA, MD ;
JOHNSON, BD ;
WISSNER, A ;
BURNS, MG ;
LARGIS, EE ;
DOLAN, JA ;
CLAUS, TH .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (16) :3081-3084
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   Evidence against β3-adrenoceptors or low affinity state of β1-adrenoceptors mediating relaxation in rat isolated aorta [J].
Brahmadevara, N ;
Shaw, AM ;
MacDonald, A .
BRITISH JOURNAL OF PHARMACOLOGY, 2003, 138 (01) :99-106
[6]  
BRAHMADEVARA N, 2003, P PHARM SOC
[7]   β1-, β2- and atypical β-adrenoceptor-mediated relaxation in rat isolated aorta [J].
Brawley, L ;
Shaw, AM ;
MacDonald, A .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 129 (04) :637-644
[8]  
CHENG Y, 1973, BIOCHEM PHARMACOL, V22, P3099
[9]   Involvement of the β3 adrenoceptor in nebivolol-induced vasorelaxation in the rat aorta [J].
de Groot, AA ;
Mathy, MJ ;
van Zwieten, PA ;
Peters, SLM .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2003, 42 (02) :232-236
[10]   MOLECULAR CHARACTERIZATION OF THE HUMAN BETA-3-ADRENERGIC RECEPTOR [J].
EMORINE, LJ ;
MARULLO, S ;
BRIENDSUTREN, MM ;
PATEY, G ;
TATE, K ;
DELAVIERKLUTCHKO, C ;
STROSBERG, AD .
SCIENCE, 1989, 245 (4922) :1118-1121