Saré Rachel Michelle, Lemons Abigail, Smith Carolyn Beebe
Section on Neuroadaptation and Protein Metabolism, Department of Health and Human Services, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, United States.
Front Neurosci. 2022 Jun 2;16:811528. doi: 10.3389/fnins.2022.811528. eCollection 2022.
Many patients with fragile X syndrome (FXS) have sleep disturbances, and knockout (KO) mice (a model of FXS) have reduced sleep duration compared to wild type (WT). Sleep is important for brain development, and chronic sleep restriction during development has long-lasting behavioral effects in WT mice. We hypothesized that the sleep abnormalities in FXS may contribute to behavioral impairments and that increasing sleep duration might improve behavior. We treated adult male KO and WT mice subacutely with three different classes of hypnotics (DORA-22, ramelteon, and zolpidem) and caffeine, a methylxanthine stimulant, and we tested the effects of treatments on sleep duration and behavior. Behavior tests included activity response to a novel environment, anxiety-like behavior, and social behavior. As expected, all hypnotics increased, and caffeine decreased sleep duration in the circadian phase in which drugs were administered. Caffeine and DORA-22 treatment significantly reduced activity in the open field regardless of genotype. Other effects were not as apparent.
许多脆性X综合征(FXS)患者存在睡眠障碍,与野生型(WT)小鼠相比,基因敲除(KO)小鼠(FXS模型)的睡眠时间缩短。睡眠对大脑发育很重要,发育过程中的慢性睡眠限制对WT小鼠具有长期的行为影响。我们假设,FXS中的睡眠异常可能导致行为障碍,延长睡眠时间可能会改善行为。我们用三类不同的催眠药(DORA-22、雷美替胺和唑吡坦)和甲基黄嘌呤兴奋剂咖啡因对成年雄性KO和WT小鼠进行亚急性治疗,并测试了这些治疗对睡眠时间和行为的影响。行为测试包括对新环境的活动反应、焦虑样行为和社交行为。正如预期的那样,在给药的昼夜节律阶段,所有催眠药都增加了睡眠时间,而咖啡因则减少了睡眠时间。无论基因型如何,咖啡因和DORA-22治疗均显著降低了旷场试验中的活动。其他影响并不明显。