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在大鼠中对临床抗焦虑性抗抑郁药的抗焦虑作用进行的两项试验。

Two tests in rats for antianxiety effect of clinically anxiety attenuating antidepressants.

作者信息

Mason P, Skinner J, Luttinger D

出版信息

Psychopharmacology (Berl). 1987;92(1):30-4. doi: 10.1007/BF00215475.

Abstract

The effects of mianserin, trazodone, amoxapine, maprotiline, and doxepin were assessed in punishment and pentylenetetrazol drug discrimination paradigms. These two procedures are used to identify antianxiety activity in rats. In the punishment procedure, misanserin produced an inverse dose-related increase in punished responding. The magnitude of the increase in punished responding with mianserin was comparable to that observed with the anxiolytic, buspirone. This effect was not observed with any of the other antidepressants tested. None of the antidepressants were found to be active in antagonizing the discriminative stimulus effects of pentylenetetrazol. In fact, at high doses there was a suggestion that the antidepressants may generalize to the pentylenetetrazol discriminative stimulus. Therefore, several antidepressants with purported clinical antianxiety activity, were not active in two procedures that detect antianxiety activity in rats.

摘要

在惩罚和戊四氮药物辨别范式中评估了米安色林、曲唑酮、阿莫沙平、马普替林和多塞平的效果。这两种程序用于识别大鼠的抗焦虑活性。在惩罚程序中,米安色林使受惩罚反应呈剂量相关的反向增加。米安色林引起的受惩罚反应增加幅度与抗焦虑药丁螺环酮观察到的幅度相当。在所测试的其他任何一种抗抑郁药中均未观察到这种效果。未发现任何一种抗抑郁药对拮抗戊四氮的辨别刺激作用有活性。事实上,在高剂量时,有迹象表明抗抑郁药可能会泛化到戊四氮辨别刺激。因此,几种据称具有临床抗焦虑活性的抗抑郁药,在检测大鼠抗焦虑活性的两种程序中均无活性。

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