Affective Disorders Program, Department of Psychology, University of Bologna, Bologna, Italy.
Prog Neuropsychopharmacol Biol Psychiatry. 2011 Aug 15;35(7):1593-602. doi: 10.1016/j.pnpbp.2010.07.026. Epub 2010 Aug 20.
There is increasing awareness that, in some cases, long-term use of antidepressant drugs (AD) may enhance the biochemical vulnerability to depression and worsen its long-term outcome and symptomatic expression, decreasing both the likelihood of subsequent response to pharmacological treatment and the duration of symptom-free periods. A review of literature suggesting potential side effects during long treatment with antidepressant drugs was performed. Studies were identified electronically using the following databases: Medline, Cinahl, PsychInfo, Web of Science and the Cochrane Library. Each database was searched from its inception date to April 2010 using "tolerance", "withdrawal", "sensitization", "antidepressants" and "switching" as key words. Further, a manual search of the psychiatric literature has been performed looking for articles pointing to paradoxical effects of antidepressant medications. Clinical evidence has been found indicating that even though antidepressant drugs are effective in treating depressive episodes, they are less efficacious in recurrent depression and in preventing relapse. In some cases, antidepressants have been described inducing adverse events such as withdrawal symptoms at discontinuation, onset of tolerance and resistance phenomena and switch and cycle acceleration in bipolar patients. Unfavorable long-term outcomes and paradoxical effects (depression inducing and symptomatic worsening) have also been reported. All these phenomena may be explained on the basis of the oppositional model of tolerance. Continued drug treatment may recruit processes that oppose the initial acute effect of a drug. When drug treatment ends, these processes may operate unopposed, at least for some time and increase vulnerability to relapse. Antidepressant drugs are crucial in the treatment of major depressive episodes. However, appraisal and testing of the oppositional model of tolerance may yield important insights as to long-term treatment and achievement of enduring effects.
人们越来越意识到,在某些情况下,长期使用抗抑郁药物(AD)可能会增强对抑郁的生化易感性,并恶化其长期预后和症状表现,降低随后对药物治疗的反应可能性和无症状期的持续时间。对长期使用抗抑郁药物可能产生的潜在副作用进行了文献回顾。使用以下关键词在以下数据库中电子检索文献:Medline、Cinahl、PsychInfo、Web of Science 和 Cochrane Library。每个数据库都从其创建日期到 2010 年 4 月进行了搜索,使用“耐受性”、“戒断”、“敏化”、“抗抑郁药”和“转换”作为关键词。此外,还对手头的精神科文献进行了手动搜索,以寻找指出抗抑郁药物的矛盾作用的文章。临床证据表明,尽管抗抑郁药在治疗抑郁发作方面有效,但在复发性抑郁和预防复发方面效果较差。在某些情况下,抗抑郁药被描述为在停药时会引起戒断症状、出现耐受性和抵抗现象以及双相患者的转换和周期加速等不良事件。还报告了不利的长期结局和矛盾作用(诱导抑郁和症状恶化)。所有这些现象都可以用对立模型的耐受性来解释。持续的药物治疗可能会招募与药物的初始急性作用相反的过程。当药物治疗结束时,这些过程可能会不受抑制地运作,至少在一段时间内会增加复发的脆弱性。抗抑郁药在治疗重性抑郁发作中至关重要。然而,对立模型的耐受性评估和测试可能会为长期治疗和获得持久效果提供重要的见解。