Volz H P, Gleiter C H, Waldmeier P C, Struck M, Möller H J
Psychiatrische Klinik and Poliklinik Friedrich-Schiller-Universität Jena, Federal Republic of Germany.
J Neural Transm (Vienna). 1996;103(1-2):217-45. doi: 10.1007/BF01292628.
The antidepressant activity of monoamine oxidase inhibitors has been well established for 30 years. Nevertheless, this group of compounds was handled with great care, mainly because of the interaction potential with tyramine-containing foodstuff. With the discovery of reversible and selective inhibitors of monoamine oxidase type A a renaissance of these compounds has begun. In this paper one of these new substances--brofaromine--will be described in detail. Biochemical and pharmacological aspects will be reviewed, showing that brofaromine is a selective and reversible inhibitor of monoamine oxidase type A with additional serotonin reuptake inhibiting properties. Both mechanisms of action may synergize in the antidepressant effect of the compound. The main results of clinical trials in depression and other indication areas will also be covered. Special attention will be put on the side effect profile.
单胺氧化酶抑制剂的抗抑郁活性已得到充分证实达30年之久。然而,这类化合物的使用一直受到严格管控,主要是因为它们与含酪胺的食物存在相互作用的潜在风险。随着可逆性和选择性A型单胺氧化酶抑制剂的发现,这类化合物迎来了复兴。本文将详细介绍其中一种新物质——溴法罗明。我们将综述其生化和药理学方面的特性,结果表明溴法罗明是一种选择性且可逆的A型单胺氧化酶抑制剂,还具有抑制5-羟色胺再摄取的特性。这两种作用机制可能在该化合物的抗抑郁效果中协同发挥作用。本文还将涵盖抑郁症及其他适应症领域的临床试验主要结果。我们将特别关注其副作用情况。