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在小鼠强迫游泳试验中,选择性5-HT7受体拮抗剂增强抗抑郁药的抗不动作用。

Enhancement of the anti-immobility action of antidepressants by a selective 5-HT7 receptor antagonist in the forced swimming test in mice.

作者信息

Wesołowska Anna, Tatarczyńska Ewa, Nikiforuk Agnieszka, Chojnacka-Wójcik Ewa

机构信息

Institute of Pharmacology, Polish Academy of Sciences, 12 Smetna Street, Kraków PL 31-343, Poland.

出版信息

Eur J Pharmacol. 2007 Jan 19;555(1):43-7. doi: 10.1016/j.ejphar.2006.10.001. Epub 2006 Oct 17.

Abstract

Using the forced swimming test in mice, we examined the effect of the following antidepressants: citalopram, imipramine, desipramine and moclobemide (which are characterized by different mechanisms of action), administered in combination with the selective 5-HT7 receptor antagonist (2R)-1-[(3-hydroxyphenyl)sulfonyl]-2-[2-(4-methyl-1-piperidinyl)ethyl]-pyrrolidine (SB 269970). All those drugs were given in doses which did not shorten the immobility time of mice. Citalopram (1.25 mg/kg), imipramine (10 mg/kg), desipramine (5 mg/kg) or moclobemide (10 mg/kg) administered jointly with SB 269970 (5 mg/kg), produced a significant antidepressant-like effect. None of the compounds studied, given alone or in combination, increased the spontaneous locomotor activity of mice. The obtained results indicate that blockade of 5-HT7 receptors may facilitate the anti-immobility effect of antidepressants in mice.

摘要

利用小鼠强迫游泳试验,我们研究了以下抗抑郁药的效果:西酞普兰、丙咪嗪、地昔帕明和吗氯贝胺(它们具有不同的作用机制),并将其与选择性5-HT7受体拮抗剂(2R)-1-[(3-羟基苯基)磺酰基]-2-[2-(4-甲基-1-哌啶基)乙基]-吡咯烷(SB 269970)联合使用。所有这些药物的给药剂量均不会缩短小鼠的不动时间。西酞普兰(1.25毫克/千克)、丙咪嗪(10毫克/千克)、地昔帕明(5毫克/千克)或吗氯贝胺(10毫克/千克)与SB 269970(5毫克/千克)联合给药时,产生了显著的抗抑郁样效果。单独或联合给予所研究的化合物,均未增加小鼠的自发运动活性。所得结果表明,阻断5-HT7受体可能会促进抗抑郁药对小鼠的抗不动效果。

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