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抗抑郁药地昔帕明、氟西汀、氟伏沙明和去甲替林可抑制人及大鼠大脑皮质组织切片对[3H]去甲肾上腺素和[3H]5-羟色胺的摄取。

The antidepressant agents desipramine, fluoxetine, fluvoxamine and norzimelidine inhibit uptake of [3H]noradrenaline and [3H]5-hydroxytryptamine in slices of human and rat cortical brain tissue.

作者信息

Harms H H

出版信息

Brain Res. 1983 Sep 19;275(1):99-104. doi: 10.1016/0006-8993(83)90421-3.

Abstract

The stability of uptake of [3H]noradrenaline and [3H]5-hydroxytryptamine in rat neocortical brain slices, prepared up to 4-5 h after decapitation, was established. Subsequently, monoamine uptake inhibition by 4 antidepressant agents: desipramine, fluoxetine, fluvoxamine and norzimelidine was compared in human post-mortem neocortical brain slices vs rat neocortical brain slices. In both species, desipramine exhibited considerable selectivity for noradrenaline uptake, while fluoxetine, fluvoxamine and norzimelidine showed varying degrees of selectivity for 5-hydroxytryptamine uptake. These results support the use of rat brain as a model for the study of neurochemical correlates of depression and antidepressant drug action.

摘要

研究确定了断头后长达4 - 5小时制备的大鼠新皮质脑片对[3H]去甲肾上腺素和[3H]5 - 羟色胺摄取的稳定性。随后,比较了4种抗抑郁药:地昔帕明、氟西汀、氟伏沙明和诺米替林在人死后新皮质脑片与大鼠新皮质脑片上对单胺摄取的抑制作用。在这两个物种中,地昔帕明对去甲肾上腺素摄取表现出相当大的选择性,而氟西汀、氟伏沙明和诺米替林对5 - 羟色胺摄取表现出不同程度的选择性。这些结果支持将大鼠脑作为研究抑郁症神经化学相关性及抗抑郁药物作用的模型。

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