非典型抗抑郁药物-精神药理学特征和作用机制。

J Maj
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引用次数: 9

摘要

研究了十种非典型新型和潜在抗抑郁药物(AD)的精神药理学特征和作用机制。研究表明,它们在药理学上是异质的。其中一些可能被认为是中枢5-羟色胺(5-HT)拮抗剂。两种典型的阿尔茨海默病,阿米替林和多西普林,也被证明是有效的5-羟色胺拮抗剂。这些观察结果证实了这些药物阻断而不是促进5-HT神经传递的结论。一些数据表明,5-羟色胺拮抗剂可以改变去甲肾上腺素能系统和血清素能系统之间的平衡,有利于前者。非典型和典型AD在长期给药时,诱导单剂量治疗后未观察到的效应。观察到的效果表明,慢性给药AD会导致去甲肾上腺素能系统的反应性增加(或激活)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Atypical antidepressant drugs - psychopharmacological profile and mechanism of action.

The psychopharmacological profile and mechanism of action of ten atypical novel and potential antidepressive drugs (AD) have been investigated. It has been shown that they form a pharmacologically heterogeneous group. Some of them may be considered as central 5-hydroxytryptamine (5-HT) antagonists. Two typical AD, amitriptyline and doxeprine, turned out to be potent 5-HT antagonists also. These observations justify the conclusion that these drugs rather block than facilitate 5-HT neurotransmission. Some data indicate that 5-HT antagonists can shift the balance between the noradrenergic and serotoninergic systems in favour of the former. Both atypical and typical AD when administered chronically, induce effects not observed after single-dose treatment. The effects observed indicate that the chronic administration of AD leads to the development of the increased responsiveness (or activation) of the noradrenergic system.

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