THE 5-HT1A RECEPTOR ANTAGONIST (S)-UH-301 BLOCKS THE (R)-8-OH-DPAT-INDUCED INHIBITION OF SEROTONERGIC DORSAL RAPHE CELL FIRING IN THE RAT

被引:29
作者
ARBORELIUS, L
HOOK, BB
HACKSELL, U
SVENSSON, TH
机构
[1] KAROLINSKA INST, DEPT PHYSIOL & PHARMACOL, DIV PHARMACOL, S-17177 STOCKHOLM, SWEDEN
[2] UPPSALA UNIV, DEPT ORGAN PHARMACEUT CHEM, UPPSALA, SWEDEN
关键词
5-HT1A; 8-OH-DPAT; (S)-UH-301; 5-HT1A RECEPTOR ANTAGONIST; ELECTROPHYSIOLOGY; DORSAL RAPHE NUCLEUS;
D O I
10.1007/BF01294785
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
(S)-UH-301 [(S)-5-fluoro-8-hydroxy-2-(dipropylamino) 0.5-4.0 mg/kg i.v.] did not significantly alter the firing rate of 5-hydroxytryptamine (5-HT) containing neurons in the dorsal raphe nucleus (DRN) as a group, although some individual cells were activated whereas others were depressed. However, (S)-UH-301 (2.0 mg/kg i.v.) consistently reversed the inhibition of DRN-5-HT cells produced by the selective 5-HT1A receptor agonist (R)-8-OH-DPAT (0.5 mu g/kg i.v.) and the dose-response curve for this effect of (R)-8-OH-DPAT was markedly shifted to the right by pretreatment with (S)-UH-301 (1.0 mg/kg i.v.). These results support the notion that (S)-UH-301 acts as an antagonist at central 5-HT1A receptors.
引用
收藏
页码:179 / 186
页数:8
相关论文
共 26 条
  • [1] SEROTONERGIC AND NON-SEROTONERGIC NEURONS OF DORSAL RAPHE - RECIPROCAL CHANGES IN FIRING INDUCED BY PERIPHERAL-NERVE STIMULATION
    AGHAJANIAN, GK
    WANG, RY
    BARABAN, J
    [J]. BRAIN RESEARCH, 1978, 153 (01) : 169 - 175
  • [2] THE 5-HT(1A) RECEPTOR SELECTIVE LIGANDS, (R)-8-OH-DPAT AND (S)-UH-301, DIFFERENTIALLY AFFECT THE ACTIVITY OF MIDBRAIN DOPAMINE NEURONS
    ARBORELIUS, L
    CHERGUI, K
    MURASE, S
    NOMIKOS, GG
    HOOK, BB
    CHOUVET, G
    HACKSELL, U
    SVENSSON, TH
    [J]. NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1993, 347 (04) : 353 - 362
  • [3] ARBORELIUS L, 1992, BEHAV PHARMACOL, V3, P40
  • [4] BJORK L, 1991, J PHARMACOL EXP THER, V258, P58
  • [5] ELECTROPHYSIOLOGICAL ASSESSMENT OF PUTATIVE ANTAGONISTS OF 5-HYDROXYTRYPTAMINE RECEPTORS - A SINGLE-CELL STUDY IN THE RAT DORSAL RAPHE NUCLEUS
    BLIER, P
    STEINBERG, S
    CHAPUT, Y
    DEMONTIGNY, C
    [J]. CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1989, 67 (02) : 98 - 105
  • [6] CHAPUT Y, 1988, J PHARMACOL EXP THER, V246, P359
  • [7] CORNFIELD LJ, 1991, MOL PHARMACOL, V39, P780
  • [8] FERRE S, 1993, J NEUROCHEM, V61, P772
  • [9] WAY100135 - A NOVEL, SELECTIVE ANTAGONIST AT PRESYNAPTIC AND POSTSYNAPTIC 5-HT(1A) RECEPTORS
    FLETCHER, A
    BILL, DJ
    BILL, SJ
    CLIFFE, IA
    DOVER, GM
    FORSTER, EA
    HASKINS, JT
    JONES, D
    MANSELL, HL
    REILLY, Y
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 237 (2-3) : 283 - 291
  • [10] THE PUTATIVE 5-HT1A RECEPTOR ANTAGONISTS NAN-190 AND BMY-7378 ARE PARTIAL AGONISTS IN THE RAT DORSAL RAPHE NUCLEUS INVITRO
    GREUEL, JM
    GLASER, T
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 211 (02) : 211 - 219