Stahl S M
Clinical Neuroscience Research Center and the Department of Psychiatry, University of California, San Diego 92122, USA.
J Clin Psychiatry. 1998;59 Suppl 4:5-14.
Distinct pharmacologic mechanisms allow the antidepressants to be separated into seven different classes. These basic pharmacologic concepts can explain not only the therapeutic actions, but also the side effects of the wide range of antidepressants currently available. The two classical mechanisms are those of tricyclic antidepressants (TCAs) and monoamine oxidase inhibitors (MAOIs). The most widely prescribed agents are the serotonin selective reuptake inhibitors (SSRIs). Three other classes of antidepressants, like the SSRIs, increase serotonergic neurotransmission, but they also have additional actions, namely dual serotonin and norepinephrine reuptake inhibition (venlafaxine); serotonin-2 antagonism/reuptake inhibition (nefazodone); and alpha2 antagonism plus serotonin-2 and -3 antagonism (mirtazapine). The selective norepinephrine and dopamine reuptake inhibitor bupropion defines a novel class of antidepressant that has no direct actions on the serotonin system.
不同的药理机制使抗抑郁药可分为七类。这些基本的药理概念不仅可以解释当前可用的各种抗抑郁药的治疗作用,还能解释其副作用。两种经典机制是三环类抗抑郁药(TCA)和单胺氧化酶抑制剂(MAOI)的机制。目前处方最广泛的药物是5-羟色胺选择性再摄取抑制剂(SSRI)。其他三类抗抑郁药与SSRI一样,可增强5-羟色胺能神经传递,但它们还有其他作用,即5-羟色胺和去甲肾上腺素双重再摄取抑制(文拉法辛);5-羟色胺-2拮抗/再摄取抑制(奈法唑酮);以及α2拮抗加5-羟色胺-2和-3拮抗(米氮平)。选择性去甲肾上腺素和多巴胺再摄取抑制剂安非他酮定义了一类新型抗抑郁药,它对5-羟色胺系统没有直接作用。