5-HT3受体激动剂SR 57227A在啮齿动物中的抗抑郁样作用。

M Poncelet, A Perio, J Simiand, G Gout, P Soubrie, G Le Fur
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引用次数: 29

摘要

我们研究了SR 57227A(一种选择性5-HT3受体激动剂,可穿过血脑屏障)对三种抗抑郁药有效的啮齿动物模型的影响。在强迫游泳试验中,sr57227a剂量依赖性地减少了小鼠和大鼠在i.p.后的不动时间。(ED50为小鼠14.2 mg/kg,大鼠7.6 mg/kg。)该化合物在口服后对两种动物均有活性。在一项小鼠时间过程研究中,sr57227a (20 mg/kg p.o)产生了持续6小时的显著效果。sr57227a(1和3 mg/kg i.p)在回避任务的最后两天使习得性无助模型大鼠逃避失败的发生率降低了50-60%,使小鼠孤立诱导的攻击率降低了50- 85%,这一效应被zacopride (1 mg/kg i.p)拮抗。这些结果表明,在啮齿动物的行为测试中,刺激5-HT3受体可以产生类似抗抑郁的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antidepressant-like effects of SR 57227A, a 5-HT3 receptor agonist, in rodents.

We have investigated the effect of SR 57227A, a selective 5-HT3 receptor agonist which crosses the blood brain barrier, on three rodent models in which antidepressants are active. In the forced swimming test, SR 57227A dose-dependently reduced the duration of immobility in mice and rats after i.p. administration. (ED50 = 14.2 mg/kg i.p. in mice, and 7.6 mg/kg i.p. in rats.) The compound was also active in both species after oral administration. In a time-course study in mice, SR 57227A (20 mg/kg p.o.) produced a significant effect lasting 6 h. SR 57227A (1 and 3 mg/kg i.p.) reduced the elevation of the escape failures in the learned helplessness model in rats by 50-60% on the last two days of the avoidance task, and reduced isolation-induced aggressivity in mice by 50 to 85%, an effect which was antagonised by zacopride (1 mg/kg i.p.). These results suggest that the stimulation of 5-HT3 receptors can produce antidepressant-like effects in behavioral tests in rodents.

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