Mylonas Dimitrios, Baran Bengi, Demanuele Charmaine, Cox Roy, Vuper Tessa C, Seicol Benjamin J, Fowler Rachel A, Correll David, Parr Elaine, Callahan Cameron E, Morgan Alexandra, Henderson David, Vangel Mark, Stickgold Robert, Manoach Dara S
Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Athinoula A. Martinos Center for Biomedical Imaging, Charlestown, MA, USA.
Neuropsychopharmacology. 2020 Dec;45(13):2189-2197. doi: 10.1038/s41386-020-00833-2. Epub 2020 Sep 12.
Sleep spindles, defining oscillations of stage 2 non-rapid eye movement sleep (N2), mediate memory consolidation. Schizophrenia is characterized by reduced spindle activity that correlates with impaired sleep-dependent memory consolidation. In a small, randomized, placebo-controlled pilot study of schizophrenia, eszopiclone (Lunesta®), a nonbenzodiazepine sedative hypnotic, increased N2 spindle density (number/minute) but did not significantly improve memory. This larger double-blind crossover study that included healthy controls investigated whether eszopiclone could both increase N2 spindle density and improve memory. Twenty-six medicated schizophrenia outpatients and 29 healthy controls were randomly assigned to have a placebo or eszopiclone (3 mg) sleep visit first. Each visit involved two consecutive nights of high density polysomnography with training on the Motor Sequence Task (MST) on the second night and testing the following morning. Patients showed a widespread reduction of spindle density and, in both groups, eszopiclone increased spindle density but failed to enhance sleep-dependent procedural memory consolidation. Follow-up analyses revealed that eszopiclone also affected cortical slow oscillations: it decreased their amplitude, increased their duration, and rendered their phase locking with spindles more variable. Regardless of group or visit, the density of coupled spindle-slow oscillation events predicted memory consolidation significantly better than spindle density alone, suggesting that they are a better biomarker of memory consolidation. In conclusion, sleep oscillations are promising targets for improving memory consolidation in schizophrenia, but enhancing spindles is not enough. Effective therapies also need to preserve or enhance cortical slow oscillations and their coordination with thalamic spindles, an interregional dialog that is necessary for sleep-dependent memory consolidation.
睡眠纺锤波是2期非快速眼动睡眠(N2)的特征性脑电振荡,介导记忆巩固。精神分裂症的特点是纺锤波活动减少,这与睡眠依赖性记忆巩固受损相关。在一项针对精神分裂症患者的小型随机、安慰剂对照试验研究中,非苯二氮䓬类镇静催眠药艾司佐匹克隆(Lunesta®)增加了N2纺锤波密度(数量/分钟),但并未显著改善记忆。这项纳入了健康对照的更大规模双盲交叉研究,调查了艾司佐匹克隆是否既能增加N2纺锤波密度又能改善记忆。26名正在接受药物治疗的精神分裂症门诊患者和29名健康对照被随机分配,先进行一次安慰剂或艾司佐匹克隆(3毫克)睡眠监测。每次监测包括连续两晚的高密度多导睡眠图监测,第二晚进行运动序列任务(MST)训练,次日上午进行测试。患者显示纺锤波密度普遍降低,并且在两组中,艾司佐匹克隆均增加了纺锤波密度,但未能增强睡眠依赖性程序性记忆巩固。后续分析显示,艾司佐匹克隆还影响皮层慢振荡:它降低了慢振荡的幅度,增加了其持续时间,并使慢振荡与纺锤波的锁相变得更具变化性。无论组别或监测顺序如何,耦合的纺锤波 - 慢振荡事件密度比单独的纺锤波密度更能显著预测记忆巩固,这表明它们是更好的记忆巩固生物标志物。总之,睡眠振荡是改善精神分裂症记忆巩固的有前景的靶点,但仅增强纺锤波是不够的。有效的治疗还需要保留或增强皮层慢振荡及其与丘脑纺锤波的协调,这种区域间对话对于睡眠依赖性记忆巩固是必要的。