Baker G B, Coutts R T, McKenna K F, Sherry-McKenna R L
Department of Psychiatry, University of Alberta, Edmonton, Canada.
J Psychiatry Neurosci. 1992 Nov;17(5):206-14.
Although the non-selective monoamine oxidase inhibitors phenelzine and tranylcypromine have been used for many years, much still remains to be understood about their mechanisms of action. Other factors, in addition to the inhibition of monoamine oxidase and the subsequent elevation of brain levels of the catecholamines and 5-hydroxytryptamine, may contribute to the overall pharmacological profiles of these drugs. This review also considers the effects on brain levels of amino acids and trace amines, uptake and release of neurotransmitter amines at nerve terminals, receptors for amino acids and amines, and enzymes other than monoamine oxidase, including enzymes involved in metabolism of other drugs. The possible contributions of metabolism and stereochemistry to the actions of these monoamine oxidase inhibitors are discussed.
尽管非选择性单胺氧化酶抑制剂苯乙肼和反苯环丙胺已被使用多年,但关于它们的作用机制仍有许多有待了解之处。除了抑制单胺氧化酶以及随后提高大脑中儿茶酚胺和5-羟色胺的水平外,其他因素可能也有助于这些药物的整体药理学特性。本综述还考虑了对大脑中氨基酸和痕量胺水平的影响、神经末梢神经递质胺的摄取和释放、氨基酸和胺的受体以及除单胺氧化酶之外的其他酶,包括参与其他药物代谢的酶。文中讨论了代谢和立体化学对这些单胺氧化酶抑制剂作用的可能贡献。