NEUROKININ A (NK2) RECEPTOR REVISITED WITH SR-48968, A POTENT NONPEPTIDE ANTAGONIST

被引:175
作者
ADVENIER, C
ROUISSI, N
NGUYEN, QT
EMONDSALT, X
BRELIERE, JC
NELIAT, G
NALINE, E
REGOLI, D
机构
[1] UNIV SHERBROOKE,FAC MED,DEPT PHARMACOL,SHERBROOKE J1H 5N1,QUEBEC,CANADA
[2] SANOFI RECH,F-31184 MONTPELLIER 04,FRANCE
[3] CEREP,F-86600 CELLE EVESCAULT,FRANCE
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0006-291X(05)80041-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SR 48968, a new non-peptide antagonist of NK2 receptors, has been tested in a variety of isolated smooth muscle preparations from rats, guinea pigs, rabbits, hamsters and men, in order to assess its selectivity for NK2 receptors as well as its competitivity and specificity. The compound has been found to be inactive as a stimulant or relaxant in all preparations but to exert a potent, competitive antagonism, particularly in tissues obtained from rabbits (pA2 9.8-10.3), guinea pigs (10.5), rats (9.4-9.6), men (9.36-9.6) and hamsters (7.45-8.6). SR 48968 is therefore more active on the NK2A than on the NK2B receptor subtype and the human receptor is close to the NK2A subtype. SR 48968 exerts an antagonism of the competitive type and is therefore suitable for receptor classification despite its slow reversibility in vitro. The sensititity of NK2A receptors to SR 48968 is at least 1000 times higher than those of NK1 and NK3 receptors. The compound does not affect the effects of bradykinin, angiotensin or bombesin. Because of its activity in human tissues, its potency and long duration of action, SR 48968 is a new promising pharmacologic and possibly therapeutic agent. © 1992 Academic Press, Inc.
引用
收藏
页码:1418 / 1424
页数:7
相关论文
共 18 条
  • [1] ADVENIER C, 1992, UNPUB
  • [2] SOME QUANTITATIVE USES OF DRUG ANTAGONISTS
    ARUNLAKSHANA, O
    SCHILD, HO
    [J]. BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1959, 14 (01): : 48 - 58
  • [3] THE TACHYKININS - A FAMILY OF PEPTIDES WITH A BROOD OF RECEPTORS
    BUCK, SH
    BURCHER, E
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 1986, 7 (02) : 65 - 68
  • [4] RECEPTORS FOR NEUROKININS IN HUMAN BRONCHUS AND URINARY-BLADDER ARE OF THE NK-2-TYPE
    DION, S
    ROUISSI, N
    NANTEL, F
    DRAPEAU, G
    REGOLI, D
    NALINE, E
    ADVENIER, C
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 178 (02) : 215 - 219
  • [5] DORLEANSJUSTE P, 1985, EUR J PHARMACOL, V125, P37
  • [6] EMONDSALT X, 1992, LIFE SCI, V50, P101
  • [7] FURCHGOTT RF, 1974, BIOCH PHARM S1, V23, P220
  • [8] MOLECULAR CHARACTERIZATION OF A FUNCTIONAL CDNA-ENCODING THE RAT SUBSTANCE-P RECEPTOR
    HERSHEY, AD
    KRAUSE, JE
    [J]. SCIENCE, 1990, 247 (4945) : 958 - 962
  • [9] PERIPHERAL EFFECTS OF NEUROKININS - FUNCTIONAL EVIDENCE FOR THE EXISTENCE OF MULTIPLE RECEPTORS
    MAGGI, CA
    GIULIANI, S
    SANTICIOLI, P
    REGOLI, D
    MELI, A
    [J]. JOURNAL OF AUTONOMIC PHARMACOLOGY, 1987, 7 (01): : 11 - 32
  • [10] COMPETITIVE ANTAGONISTS DISCRIMINATE BETWEEN NK2 TACHYKININ RECEPTOR SUBTYPES
    MAGGI, CA
    PATACCHINI, R
    GIULIANI, S
    ROVERO, P
    DION, S
    REGOLI, D
    GIACHETTI, A
    MELI, A
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 1990, 100 (03) : 588 - 592