Antidepressant-like effect of the selective 5-HT1B receptor agonist CP 94253:: A possible mechanism of action

被引:42
|
作者
Tatarczynska, E [1 ]
Antkiewicz-Michaluk, L [1 ]
Klodzinska, A [1 ]
Stachowicz, K [1 ]
Chojnacka-Wójcik, E [1 ]
机构
[1] Polish Acad Sci, Inst Pharmacol, PL-31343 Krakow, Poland
关键词
5-HT1B receptor ligand; p-Chlorophenylalanine; idazoxan; sulpiride; forced swimming test in mice;
D O I
10.1016/j.ejphar.2005.04.025
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The mechanism of the antidepressant-like activity of the selective 5-hydroxytryptamine(1B) (5-HT1B) receptor agonist 5-propoxy-3(1,2,3,6-tetrahydro-4-pyridinyl)-1H-pyrrolo[3,2-b]pyridine (CP 94253) was studied in the forced swimming test in mice. CP 94253 administered intraperitoneally at a single dose of 5 mg/kg potently shortened the immobility time of mice. The anti-immobility effect of CP 94253 was wholly blocked by the selective 5-HT1B receptor antagonist N-[3-(2-dimethylamino)ethoxy-4-methoxyphenyl]-2'-methyl-4'-(5methyl-1,2,4-oxadiazol-3-yl)-(1, 1'-biphenyl)-4-carboxamide (SB 216641, 5 mg/kg), the dopamine D2-like receptor antagonist sulpiride (50 mg/kg) and the alpha(2)-adrenoceptor antagonist idazoxan (2 mg/kg), but was not modified in animals with a lesion of the 5-HT system produced by p-chlorophenylalanine (p-CPA, 3 x 300 mg/kg). The obtained results suggest that the anti-immobility effect of CP 94253 is mediated by activation of 5-HT1B receptors-most probably located postsynaptically and/or as heteroreceptors, and that the dopamine and the noradrenaline systems are involved in this action. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:46 / 50
页数:5
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