Winokur A, Gary K A, Rodner S, Rae-Red C, Fernando A T, Szuba M P
Department of Psychiatry, School of Medicine, University of Connecticut Health Center, Farmington, Connecticut, USA.
Depress Anxiety. 2001;14(1):19-28. doi: 10.1002/da.1043.
This review summarizes current findings regarding effects of antidepressant compounds on sleep architecture and interprets their clinical relevance. Effects of the major classes of antidepressant drugs on sleep properties are presented, with the antidepressant compounds organized into categories based primarily on their putative mechanism of action. The majority of antidepressant compounds, across several different categories, exhibit robust suppression of REM sleep. Others, such as bupropion and nefazodone, lack REM suppressant effects. Such findings support the idea that critical neurochemical mechanisms involved in the regulation of discrete sleep stages can be elucidated by means of polysomnographic investigations utilizing pharmacologically targeted agents. Clinicians have appreciated the importance of antidepressant drug effects on sleep when considering therapeutic options for patients. While such decisions in the past were based on empirical observations, an increasing amount of information regarding specific effects of different antidepressant drugs on sleep continuity and sleep architecture is available. Thus, clinicians may choose to consider profiles of sleep effects for different antidepressant drugs in the initial selection of an antidepressant compound.
本综述总结了有关抗抑郁化合物对睡眠结构影响的当前研究结果,并阐释了其临床相关性。文中介绍了主要类别抗抑郁药物对睡眠特性的影响,这些抗抑郁化合物主要根据其假定的作用机制进行分类。在几个不同类别中,大多数抗抑郁化合物都能显著抑制快速眼动(REM)睡眠。其他药物,如安非他酮和奈法唑酮,则缺乏抑制REM睡眠的作用。这些发现支持了这样一种观点,即通过使用药理靶向药物的多导睡眠图研究,可以阐明参与调节离散睡眠阶段的关键神经化学机制。临床医生在为患者考虑治疗方案时,已经认识到抗抑郁药物对睡眠的影响的重要性。虽然过去此类决策基于经验观察,但现在有越来越多关于不同抗抑郁药物对睡眠连续性和睡眠结构的具体影响的信息。因此,临床医生在最初选择抗抑郁化合物时,可能会选择考虑不同抗抑郁药物的睡眠影响特征。