Andrews J M, Nemeroff C B
Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Georgia 30322-4990.
Am J Med. 1994 Dec 19;97(6A):24S-32S. doi: 10.1016/0002-9343(94)90360-3.
Major depression is a common and disabling disorder with far-reaching social and economic implications. Nonetheless, major depression is treatable by one of the many currently available antidepressants with response rates of approximately 65-70%. Treatment of depression has improved in recent years because of the availability of effective and well-tolerated antidepressants, such as the selective serotonin reuptake inhibitors (SSRIs). The currently available antidepressants are generally equally effective and are distinguished primarily by side-effect profiles. The side effects of tricyclic antidepressants (TCAs) are attributed to their nonspecific interaction with cholinergic, histaminergic, serotonergic, and dopaminergic receptors in the central nervous system. The secondary amine TCAs, nortriptyline and desipramine, are preferred among the TCAs because of a more favorable side-effect profile. The TCAs are cardiotoxic, and overdoses are frequently fatal. Adverse effects, including potentially fatal drug and food interactions, limit the use of the monoamine oxidase inhibitors (MAOIs); however, these agents have a role in the treatment of depression with comorbid anxiety, refractory depression, atypical depression, and bulimia. The SSRIs possess a class side-effect profile of headache, nausea, and sexual dysfunction. Individual differences in side effects may distinguish fluoxetine (nervousness, restlessness), sertraline (diarrhea, loose stools), and paroxetine (dry mouth). The SSRIs all inhibit certain cytochrome P450 isoenzymes involved in the metabolism of drugs, such as the TCAs, and each SSRI has been reported to increase plasma concentrations of concomitantly administered TCAs. Bupropion therapy is associated with a risk of seizure development, which can be minimized by multiple daily doses. Trazodone is sedating and can rarely cause priapism. The related compound, nefazodone, does not cause sexual dysfunction or priapism, but is associated with sedation. Venlafaxine, a recently available antidepressant that appears to have efficacy in treatment-refractory depression, may cause nausea that requires gradual upward dosage titration. Higher doses of venlafaxine may also cause elevations in blood pressure, heart rate, and serum cholesterol. As more is learned about the pathophysiology of depression, even more specific and well-tolerated antidepressants will be developed.
重度抑郁症是一种常见且使人丧失能力的疾病,具有深远的社会和经济影响。尽管如此,重度抑郁症可通过目前众多可用的抗抑郁药物之一进行治疗,有效率约为65%-70%。近年来,由于有了有效且耐受性良好的抗抑郁药物,如选择性5-羟色胺再摄取抑制剂(SSRI),抑郁症的治疗有了改善。目前可用的抗抑郁药物通常同样有效,主要区别在于副作用情况。三环类抗抑郁药(TCA)的副作用归因于它们与中枢神经系统中的胆碱能、组胺能、5-羟色胺能和多巴胺能受体的非特异性相互作用。在三环类抗抑郁药中,二级胺类的去甲替林和地昔帕明因其副作用情况较为有利而更受青睐。三环类抗抑郁药具有心脏毒性,过量服用往往致命。包括潜在致命的药物和食物相互作用在内的不良反应限制了单胺氧化酶抑制剂(MAOI)的使用;然而,这些药物在治疗伴有焦虑、难治性抑郁症、非典型抑郁症和贪食症的抑郁症方面有一定作用。选择性5-羟色胺再摄取抑制剂的类副作用包括头痛、恶心和性功能障碍。副作用的个体差异可能使氟西汀(紧张、坐立不安)、舍曲林(腹泻、大便稀溏)和帕罗西汀(口干)有所不同。所有选择性5-羟色胺再摄取抑制剂都会抑制某些参与药物代谢的细胞色素P450同工酶,如三环类抗抑郁药,并且据报道每种选择性5-羟色胺再摄取抑制剂都会增加同时服用的三环类抗抑郁药的血浆浓度。安非他酮治疗有引发癫痫的风险,通过每日多次给药可将这种风险降至最低。曲唑酮有镇静作用,很少会引起阴茎异常勃起。相关化合物奈法唑酮不会引起性功能障碍或阴茎异常勃起,但有镇静作用。文拉法辛是一种最近可用的抗抑郁药,似乎对难治性抑郁症有效,可能会引起恶心,这需要逐渐增加剂量。较高剂量的文拉法辛也可能导致血压、心率和血清胆固醇升高。随着对抑郁症病理生理学了解的增多,将会研发出更具特异性且耐受性更好的抗抑郁药物。