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安非他酮治疗价值的药理学基础。

The pharmacologic basis for therapeutic interest in bupropion.

作者信息

Soroko F E, Maxwell R A

出版信息

J Clin Psychiatry. 1983 May;44(5 Pt 2):67-73.

PMID:6406467
Abstract

Bupropion, a compound chemically dissimilar to tricyclic antidepressants and monoamine oxidase inhibitors, was found to be active in animal models that are predictive of antidepressant activity in man. Bupropion was also found to be pharmacologically and biochemically distinct from tricyclics and monoamine oxidase inhibitors. Furthermore, it lacked anticholinergic activity, was not sympathomimetic, and was at least 10-fold weaker as a cardiac depressant than the tricyclic antidepressants. It was concluded that bupropion would be better tolerated and safer in man than standard therapies and that its pharmacologic and biochemical profile held out the possibility of novel antidepressant actions.

摘要

安非他酮是一种化学结构与三环类抗抑郁药和单胺氧化酶抑制剂不同的化合物,发现在可预测对人类抗抑郁活性的动物模型中具有活性。还发现安非他酮在药理和生化方面与三环类药物和单胺氧化酶抑制剂不同。此外,它没有抗胆碱能活性,没有拟交感神经活性,作为心脏抑制剂的作用比三环类抗抑郁药至少弱10倍。得出的结论是,与标准疗法相比,安非他酮在人体中耐受性更好、更安全,并且其药理和生化特性表明它有可能具有新型抗抑郁作用。

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