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米安色林在抗抑郁药中的地位(作者译)

[The place of mianserin among the antidepressants (author's transl)].

作者信息

De Buck R

出版信息

Acta Psychiatr Belg. 1978 Sep-Oct;78(5):841-54.

PMID:375688
Abstract

The originality of mianserin lies mainly in its chemical formula ; it is a tetracyclic piperazino-azepine compound. Moreover its pharmacological profile differs from that of other antidepressant drugs because it is devoid of central anticholinergic effects, it inhibits 5-hydroxytryptophane (the precursor of serotonine) and contrary to the tricyclics it does not affect the re-uptake of the amine-transmitters but increases the turnover of noradrenaline. It has been shown in a clinical trial that mianserin induces a hypomania in some manic-depressed patients. Regarding the antidepressive effect, mianserin is superior to placebo and as effective as imipramine and amitriptyline. It simultaneously works on anxiety, psychomotoric retardation and suicidal tendency; sleep improves under mianserin's influence. The value of mianserin is proved by its safety in use. It has no cardiotoxic effect and does not interact with coumarin-type anticoagulants. Since there are no anticholinergic effects, mianserin can be given to patients suffering from glaucoma or prostatic hypertrophy. Finally it appears that mianserin lowers the suicidal risk through its sedative properties.

摘要

米安色林的独特之处主要在于其化学分子式;它是一种四环哌嗪并氮杂卓化合物。此外,其药理特性与其他抗抑郁药物不同,因为它没有中枢抗胆碱能作用,能抑制5-羟色氨酸(血清素的前体),并且与三环类药物相反,它不影响胺类递质的再摄取,而是增加去甲肾上腺素的更新率。一项临床试验表明,米安色林会在一些躁郁症患者中诱发轻躁狂。关于抗抑郁作用,米安色林优于安慰剂,与丙咪嗪和阿米替林效果相当。它同时对焦虑、精神运动性迟缓及自杀倾向有效;在米安色林的作用下睡眠会得到改善。米安色林的安全性证明了其价值。它没有心脏毒性作用,也不与香豆素类抗凝剂相互作用。由于没有抗胆碱能作用,米安色林可用于青光眼或前列腺肥大患者。最后,米安色林似乎因其镇静特性降低了自杀风险。

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