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米安色林:十年科学发展历程

Mianserin: a decade of scientific development.

作者信息

Peet M, Behagel H

出版信息

Br J Clin Pharmacol. 1978;5 Suppl 1(Suppl 1):5S-9S.

Abstract

1 Mianserin is a tetracyclic piperazino-azepine compound synthesized in 1966 for its peripheral anti 5-hydroxytryptamine properties. Animal screening showed that mianserin was centrally active, but the profile did not indicate possible antidepressant activity. Following clinical observations of sedative and possible mood-lifting effects, a quantitative electroencephalogram (EEG) study showed that the EEG effects of mianserin are similar to those of amitriptyline. 2 Subsequent clinical and pharmacological studies have indicated that mianserin is an effective antidepressant which differs from the tricyclic antidepressants not only chemically but also in its pharmacological and clinical profile. Mianserin seems to lack anticholinergic and cardiotoxic properties, and has unusual effects on monoamine metabolism. 3 On the basis of the initial profile a series of clinical and pharmacological studies has been carried out, and the results of many of these studies are presented in these Proceedings.

摘要
  1. 米安色林是一种四环哌嗪并氮杂卓化合物,于1966年合成,因其具有外周抗5-羟色胺特性。动物筛选表明米安色林具有中枢活性,但其特性未显示出可能的抗抑郁活性。在对其镇静和可能的情绪提升作用进行临床观察后,一项定量脑电图(EEG)研究表明,米安色林对脑电图的影响与阿米替林相似。2. 随后的临床和药理学研究表明,米安色林是一种有效的抗抑郁药,它不仅在化学结构上,而且在药理和临床特性上都与三环类抗抑郁药不同。米安色林似乎缺乏抗胆碱能和心脏毒性特性,并且对单胺代谢有不同寻常的影响。3. 根据最初的特性开展了一系列临床和药理学研究,其中许多研究的结果在这些论文集中呈现。

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A pharmacokinetic study of mianserin.米安色林的药代动力学研究。
Eur J Clin Pharmacol. 1982;21(6):517-20. doi: 10.1007/BF00542048.
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The pharmacology of mianserin--an update.米安色林的药理学——最新进展
Br J Clin Pharmacol. 1983;15 Suppl 2(Suppl 2):263S-268S. doi: 10.1111/j.1365-2125.1983.tb05874.x.

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Development of psychotropic drugs.
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