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单胺氧化酶及其抑制剂的现状

The current status of monoamine oxidase and its inhibitors.

作者信息

Jarrott B, Vajda F J

出版信息

Med J Aust. 1987 Jun 15;146(12):634-8. doi: 10.5694/j.1326-5377.1987.tb120442.x.

DOI:10.5694/j.1326-5377.1987.tb120442.x
PMID:3114597
Abstract

The enzyme monoamine oxidase (MAO) plays an important role in the inactivation of both dietary amines and also of neurotransmitter amines. A study of the properties of irreversible inhibitors of this enzyme suggests that the enzyme exists in two broad types--MAO-A and MAO-B. Although irreversible inhibitors of MAO were once widely used as antidepressant agents, they fell from favour because of adverse reactions after the ingestion of amine-containing foodstuffs ("the cheese reaction"). However, these inhibitors (phenelzine and tranylcypromine) are probably best for the treatment of atypical depression providing the patient is aware of dietary reactions. A new series of reversible, MAO-A selective inhibitors are being developed which do not exhibit serious dietary interactions. These reversible inhibitors show promise as rapidly acting antidepressant agents. An atypical irreversible MAO-B selective inhibitor, selegiline (deprenyl) does not exhibit an adverse reaction on the ingestion of amine-containing foods. This drug has been used as an adjuvant in the treatment of Parkinson's disease since it allows the dose of L-dopa to be reduced by approximately 25%. More important, selegiline may slow the degeneration of dopaminergic neurons that is characteristic of Parkinson's disease.

摘要

单胺氧化酶(MAO)在膳食胺和神经递质胺的失活过程中都起着重要作用。一项关于该酶不可逆抑制剂性质的研究表明,该酶存在两种主要类型——MAO - A和MAO - B。尽管MAO的不可逆抑制剂曾被广泛用作抗抑郁药,但由于摄入含胺食物后会出现不良反应(“奶酪反应”),它们逐渐失宠。然而,如果患者了解饮食反应,这些抑制剂(苯乙肼和反苯环丙胺)可能最适合治疗非典型抑郁症。一系列新型的、可逆的、MAO - A选择性抑制剂正在研发中,它们不会表现出严重的饮食相互作用。这些可逆抑制剂有望成为快速起效的抗抑郁药。一种非典型的不可逆MAO - B选择性抑制剂,司来吉兰(丙炔苯丙胺)在摄入含胺食物时不会出现不良反应。这种药物自允许将左旋多巴的剂量减少约25%以来,一直被用作帕金森病治疗的辅助药物。更重要的是,司来吉兰可能会减缓帕金森病特有的多巴胺能神经元的退化。

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The current status of monoamine oxidase and its inhibitors.单胺氧化酶及其抑制剂的现状
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2
SR 95191, a selective inhibitor of type A monoamine oxidase with dopaminergic properties. II. Biochemical characterization of monoamine oxidase inhibition.SR 95191,一种具有多巴胺能特性的A型单胺氧化酶选择性抑制剂。II. 单胺氧化酶抑制作用的生化特性
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Comparison of the effects of moclobemide and selegiline on tyramine-evoked mydriasis in man.吗氯贝胺与司来吉兰对人体中酪胺诱发瞳孔散大影响的比较。
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(-)-Deprenyl, a selective MAO-B inhibitor, with apoptotic and anti-apoptotic properties.(-)-司来吉兰,一种选择性单胺氧化酶-B抑制剂,具有促凋亡和抗凋亡特性。
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[Comparison of the new MAO-A inhibitors moclobemide, brofaromine and toloxatone with tranylcypromine in an animal experiment: significance for clinical practice].[新型单胺氧化酶-A抑制剂吗氯贝胺、溴法罗明和托洛沙酮与反苯环丙胺在动物实验中的比较:对临床实践的意义]
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Inhibition of monoamine oxidase type A, but not type B, is an effective means of inducing anticonvulsant activity in the kindling model of epilepsy.抑制A型单胺氧化酶而非B型单胺氧化酶,是在癫痫点燃模型中诱导抗惊厥活性的有效手段。
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The therapeutic potential of moclobemide, a reversible selective monoamine oxidase A inhibitor in Parkinson's disease.莫洛贝胺(一种可逆性选择性单胺氧化酶A抑制剂)在帕金森病中的治疗潜力。
J Clin Psychopharmacol. 1995 Aug;15(4 Suppl 2):51S-59S. doi: 10.1097/00004714-199508001-00010.

引用本文的文献

1
Inhibition of monoamine oxidase by moclobemide: effects on monoamine metabolism and secretion of anterior pituitary hormones and cortisol in healthy volunteers.吗氯贝胺对单胺氧化酶的抑制作用:对健康志愿者单胺代谢、垂体前叶激素分泌及皮质醇的影响
Br J Clin Pharmacol. 1989 Feb;27(2):243-55. doi: 10.1111/j.1365-2125.1989.tb05357.x.