Anxiolytic action of a neurokinin(1) receptor antagonist in the social interaction test

被引:98
作者
File, SE
机构
[1] Psychopharmacology Research Unit, UMDS, Guy's Hospital, SE1 9RT, London
关键词
substance P; NK1; receptors; CGP; 49823; anxiety; social interaction; tolerance; withdrawal;
D O I
10.1016/S0091-3057(97)90002-2
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
CGP 49823, a substance P antagonist acting at NK, receptors, had significant anxiolytic effects at 3, 10 and 30 mg/kg orally in the high-light unfamiliar and low-light unfamiliar conditions of the social interaction test but was without effect in the low-light familiar condition. The effects were less marked after 3 and 6 weeks of treatment (10 mg/kg/day), indicating that some tolerance had developed, but a significant anxiolytic effect still remained. After 3 weeks of diazepam treatment (2 mg/kg/day, intraperitoneally), tolerance developed to the anxiolytic effects, and there was an anxiogenic response 24 h after withdrawal. In contrast, there were no anxiogenic withdrawal effects 24 h after 3 weeks or 24, 48 or 72 h after 6 weeks treatment with CGP 49323 (10 mg/kg/day). These results suggest that the compound may prove to be a useful anxiolytic and that substance P may play a role in mediating states of anxiety. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:747 / 752
页数:6
相关论文
共 31 条
[11]   THE HISTORY OF BENZODIAZEPINE DEPENDENCE - A REVIEW OF ANIMAL STUDIES [J].
FILE, SE .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1990, 14 (02) :135-146
[12]  
FILE SE, 1990, EUR J PHARMACOL, V190, P229
[13]  
File SE, 1996, J NEUROSCI, V16, P4810
[14]   CHRONIC EXPOSURE TO NOISE MODIFIES THE ANXIOGENIC RESPONSE, BUT NOT THE HYPOACTIVITY, DETECTED ON WITHDRAWAL FROM CHRONIC ETHANOL TREATMENT [J].
FILE, SE .
PSYCHOPHARMACOLOGY, 1994, 116 (03) :369-372
[15]  
FILE SE, 1993, SOCIAL INTERACTION T
[16]  
GARRET C, 1991, P NATL ACAD SCI USA, V88, P1020
[17]   5-HT1A and benzodiazepine receptors in the basolateral amygdala modulate anxiety in the social interaction test, but not in the elevated plus-maze [J].
Gonzalez, LE ;
Andrews, N ;
File, SE .
BRAIN RESEARCH, 1996, 732 (1-2) :145-153
[18]  
Hasenoehrl R. U., 1996, Society for Neuroscience Abstracts, V22, P1152
[19]  
Hauser K., 1994, Neuropeptides, V26, P37, DOI 10.1016/0143-4179(94)90228-3
[20]   DIVERSITY IN MAMMALIAN TACHYKININ PEPTIDERGIC NEURONS - MULTIPLE PEPTIDES, RECEPTORS, AND REGULATORY MECHANISMS [J].
HELKE, CJ ;
KRAUSE, JE ;
MANTYH, PW ;
COUTURE, R ;
BANNON, MJ .
FASEB JOURNAL, 1990, 4 (06) :1606-1615