Effects of 8-OHDPAT and 5-HT1A antagonists WAY100135 and WAY100635, on guinea-pig behaviour and dorsal raphe 5-HT neurone firing

被引:83
作者
Mundey, MK
Fletcher, A
Marsden, CA
机构
[1] UNIV NOTTINGHAM,QUEENS MED CTR,SCH MED,DEPT PHYSIOL & PHARMACOL,NOTTINGHAM NG7 2UH,ENGLAND
[2] WYETH RES UK LTD,MAIDENHEAD SL6 0PH,BERKS,ENGLAND
关键词
5-HT1A antagonists; dorsal raphe nucleus; somatodendritic autoreceptor; behavioural syndrome in guinea-pig; 8-OHDPAT; WAY100135; WAY100635;
D O I
10.1111/j.1476-5381.1996.tb15254.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 The effects of 5-HT1A antagonists on guinea-pig behaviour and dorsal raphe neuronal activity were investigated. 2 WAY100135 (10 mg kg(-1) s.c.) and WAY100635 (1mg kg(-1) s.c.) significantly reduced the behaviours induced by 8-hydroxy-2-(di-n-propylamino) tetralin (8-OHDPAT) (1 mg kg(-1), s.c.) indicative of post-synaptic 5-HT1A receptor antagonism. WAY100635 (10 mg kg(-1), s.c.) alone induced ear twitches, which were antagonized by ketanserin (1 mg kg(-1), s.c.), but no other overt behaviours. 3 WAY100635 (0.125 mg kg(-1) i.v.) produced a right-ward shift in the dose-related inhibition of neuronal firing by 8-OHDPAT (5-100 mu g kg(-1), i.v.) but did not affect the maximum inhibition induced by 8-OHDPAT indicating competitive antagonism between 8-OHDPAT and WAY100635 at the 5-HT1A somato-dendritic autoreceptor in the dorsal raphe nucleus of the guinea-pig. WAY100635 also produced a dose-related increase in the basal firing of 5-HT neurones in the dorsal raphe nucleus and restored the firing of dorsal raphe neurones previously inhibited by 8-OHDPAT (10 mu g kg(-1), i.v.). 4 The results indicate that WAY100635 is a competitive 5-HT1A antagonist in the guinea-pig. Furthermore WAY100635 can increase 5-HT neuronal firing, suggesting that it blocks a 5-HT1A receptor-mediated inhibitory tone acting on guinea-pig 5-HT neurones resulting in increased 5-HT release and 5-HT2 receptor-mediated behaviours.
引用
收藏
页码:750 / 756
页数:7
相关论文
共 41 条
[1]  
ARBORELLUS L, 1992, SEROTONIN ANIMAL MOD, V3, P12
[2]   8-HYDROXY-2-(DI-NORMAL-PROPYLAMINO)TETRALIN, A NEW CENTRALLY ACTING 5-HYDROXYTRYPTAMINE RECEPTOR AGONIST [J].
ARVIDSSON, LE ;
HACKSELL, U ;
NILSSON, JLG ;
HJORTH, S ;
CARLSSON, A ;
LINDBERG, P ;
SANCHEZ, D ;
WIKSTROM, H .
JOURNAL OF MEDICINAL CHEMISTRY, 1981, 24 (08) :921-923
[3]   5-HT2 RECEPTOR SUBTYPES - A FAMILY RE-UNITED [J].
BAXTER, G ;
KENNETT, G ;
BLANEY, F ;
BLACKBURN, T .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1995, 16 (03) :105-110
[4]   WET-DOG SHAKE BEHAVIOR IN RAT - POSSIBLE QUANTITATIVE MODEL OF CENTRAL 5-HYDROXYTRYPTAMINE ACTIVITY [J].
BEDARD, P ;
PYCOCK, CJ .
NEUROPHARMACOLOGY, 1977, 16 (10) :663-670
[5]  
BJORK L, 1991, J PHARMACOL EXP THER, V258, P58
[6]   5-HYDROXYTRYPTOPHAN-INDUCED MYOCLONUS IN GUINEA-PIGS - PHYSIOLOGICAL AND PHARMACOLOGICAL INVESTIGATION [J].
CHADWICK, D ;
HALLETT, M ;
JENNER, P ;
MARSDEN, CD .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1978, 35 (01) :157-165
[7]   EFFECTS OF PUTATIVE 5-HYDROXYTRYPTAMINE ANTAGONISTS ON BEHAVIOR PRODUCED BY ADMINISTRATION OF TRANYLCYPROMINE AND L-TRYPTOPHAN OR TRANYLCYPROMINE AND L-DOPA TO RATS [J].
DEAKIN, JFW ;
GREEN, AR .
BRITISH JOURNAL OF PHARMACOLOGY, 1978, 64 (02) :201-209
[8]   CHARACTERISTICS OF FEEDING INDUCED BY THE SEROTONIN AGONIST "8-HYDROXY-2-(DI-NORMAL-PROPYLAMINO) TETRALIN (8-OH-DPAT) [J].
DOURISH, CT ;
HUTSON, PH ;
CURZON, G .
BRAIN RESEARCH BULLETIN, 1985, 15 (04) :377-384
[9]   SILENT 5-HT(1A)-RECEPTOR ANTAGONISTS - UTILITY AS RESEARCH TOOLS AND THERAPEUTIC AGENTS [J].
FLETCHER, A ;
CLIFFE, IA ;
DOURISH, CT .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1993, 14 (12) :441-448
[10]   WAY100135 - A NOVEL, SELECTIVE ANTAGONIST AT PRESYNAPTIC AND POSTSYNAPTIC 5-HT(1A) RECEPTORS [J].
FLETCHER, A ;
BILL, DJ ;
BILL, SJ ;
CLIFFE, IA ;
DOVER, GM ;
FORSTER, EA ;
HASKINS, JT ;
JONES, D ;
MANSELL, HL ;
REILLY, Y .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 237 (2-3) :283-291