8-OH-DPAT-INDUCED CORTICOSTERONE SECRETION AS AN INVIVO MODEL OF 5-HT1A RECEPTOR FUNCTION

被引:6
作者
RIVET, JM [1 ]
MILLAN, MJ [1 ]
COLPAERT, FC [1 ]
机构
[1] FONDAX GRP RECH SERV,DIV NEUROBIOL,F-92800 PUTEAUX,FRANCE
关键词
D O I
10.1016/0014-2999(90)92473-V
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
引用
收藏
页码:684 / 685
页数:2
相关论文
共 50 条
[21]   Investigation of mechanisms mediating 8-OH-DPAT-induced impairment of spatial memory:: Involvement of 5-HT1A receptors in the dorsal hippocampus in rats [J].
Egashira, N ;
Yano, A ;
Ishigami, N ;
Mishima, K ;
Iwasaki, K ;
Fujioka, M ;
Matsushita, M ;
Nishimura, R ;
Fujiwara, M .
BRAIN RESEARCH, 2006, 1069 (01) :54-62
[22]   Effects of WAY 100635 and (-)-5-Me-8-OH-DPAT, a novel 5-HT1A receptor antagonist, on 8-OH-DPAT responses [J].
Trillat, AC ;
Malagié, I ;
Mathé-Allainmat, M ;
Anmela, MC ;
Jacquot, C ;
Langlois, M ;
Gardier, AM .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 347 (01) :41-49
[23]   8-OH-DPAT-induced release of hippocampal noradrenaline in vivo: Evidence for a role of both 5-HT1A and dopamine D-1 receptors [J].
HajosKorcsok, E ;
Sharp, T .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 314 (03) :285-291
[24]   ESTRADIOL MODULATION OF THE HYPERPHAGIA INDUCED BY THE 5-HT1A AGONIST, 8-OH-DPAT [J].
SALAMANCA, S ;
UPHOUSE, L .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1992, 43 (03) :953-955
[25]   STIMULATION OF CORTICOSTERONE SECRETION BY THE SELECTIVE 5-HT1A RECEPTOR AGONIST 8-HYDROXY-2-(DI-N-PROPYLAMINO)TETRALIN (8-OH-DPAT) IN THE RAT [J].
PRZEGALINSKI, E ;
BUDZISZEWSKA, B ;
WARCHOLKANIA, A ;
BLASZCZYNSKA, E .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1989, 33 (02) :329-334
[26]   THE NOVEL 5-HT1A RECEPTOR ANTAGONIST (S)-UH-301 PREVENTS (R)-8-OH-DPAT-INDUCED DECREASE IN INTERSTITIAL CONCENTRATIONS OF SEROTONIN IN THE RAT HIPPOCAMPUS [J].
NOMIKOS, GG ;
ARBORELIUS, L ;
SVENSSON, TH .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 216 (03) :373-378
[27]   (-)-5-Me-8-OH-DPAT, a new silent and full 5-HT1A receptor antagonist [J].
Trillat, AC ;
Mathé-Allainmat, M ;
Malagié, I ;
Jacquot, C ;
Langlois, M ;
Gardier, AM .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1998, 358 (01) :R106-R106
[28]   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 [J].
ARBORELIUS, L ;
HOOK, BB ;
HACKSELL, U ;
SVENSSON, TH .
JOURNAL OF NEURAL TRANSMISSION-GENERAL SECTION, 1994, 96 (03) :179-186
[29]   THE 5-HT1A RECEPTOR AGONIST, 8-OH-DPAT, PREFERENTIALLY ACTIVATES CELL BODY 5-HT AUTORECEPTORS IN RAT-BRAIN INVIVO [J].
HJORTH, S ;
MAGNUSSON, T .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1988, 338 (05) :463-471
[30]   COUNTERACTION OF THE RAPID TOLERANCE TO 8-OH-DPAT-INDUCED CORTICOSTERONE SECRETION IN RATS BY ACTIVATION OF THE GABA-A RECEPTOR-CHLORIDE CHANNEL COMPLEX [J].
KELDER, D ;
ROSS, SB .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 109 (01) :207-212