Stewart Lee S, Persinger Michael A, Cortez Miguel A, Snead O Carter
Brain and Behavior Research Program, The Hospital for Sick Children, 555 University Avenue, Toronto, ON, Canada.
Behav Genet. 2007 Mar;37(2):388-98. doi: 10.1007/s10519-006-9119-y. Epub 2006 Dec 5.
Disruption of the sleep-wake cycle has been reported among individuals with Down syndrome (DS). Here we studied behavioral rhythms in adult male and female Ts65Dn mice, a model of DS. The overall behavioral activity of Ts65Dn and diploid (2N) littermates as defined by total movements (TM), movement time (MT), ambulatory movement time (AMT), time spent in center of arena (CT), jumps (JFP), rotational behavior (TURNS), and wheel-running activity (WRA) was recorded under a 12 h:12 h light-dark photocycle. During the light phase, Ts65Dn mice exhibited higher TM, MT, CT, JFP, and WRA compared to 2N littermates. During the dark phase, Ts65Dn and 2N mice differed only in CT and WRA, with the Ts65Dn group engaging in higher levels of both. There were no gender differences for any of the behavioral variables studied. Non-linear least-squares (Cosinor) analysis of the distribution of total behavioral activity (TM) indicated that Ts65Dn mice exhibited a slightly higher mean oscillation (i.e., mesor), but significantly lower amplitude in comparison to 2N mice, suggesting that levels of TM were elevated in trisomic mice but were relatively constant throughout the photocycle. The peak of the Ts65Dn TM rhythm was significantly phase-advanced, occurring approximately 4 h earlier than 2N mice. Overall, Ts65Dn mice were hyperactive and differed significantly in daily patterns of specific behaviors from those of 2N littermates. To control for the potential confound of retinal degeneration in Ts65Dn and 2N mice, we compared and found no difference between the TM rhythm parameters of 2N and non-retinally degenerate C57/129Sv mice, suggesting that abnormal behavioral rhythmicity in Ts65Dn mice may not due to the absence of rod and cone photoreceptors. These results serve as a starting point for further investigations into the physiological basis of sleep-wake disturbances in DS patients.
据报道,唐氏综合征(DS)患者存在睡眠-觉醒周期紊乱的情况。在此,我们研究了成年雄性和雌性Ts65Dn小鼠(一种DS模型)的行为节律。在12小时光照:12小时黑暗的光周期下,记录了Ts65Dn小鼠和二倍体(2N)同窝小鼠的总体行为活动,这些活动通过总运动量(TM)、运动时间(MT)、自主运动时间(AMT)、在竞技场中心停留的时间(CT)、跳跃次数(JFP)、旋转行为(TURNS)和轮转活动(WRA)来定义。在光照阶段,与2N同窝小鼠相比,Ts65Dn小鼠表现出更高的TM、MT、CT、JFP和WRA。在黑暗阶段,Ts65Dn小鼠和2N小鼠仅在CT和WRA方面存在差异,Ts65Dn组在这两方面的水平更高。所研究的任何行为变量均无性别差异。对总行为活动(TM)分布的非线性最小二乘法(Cosinor)分析表明,与2N小鼠相比,Ts65Dn小鼠表现出略高的平均振荡(即中值),但振幅显著较低,这表明三体小鼠的TM水平升高,但在整个光周期内相对恒定。Ts65Dn小鼠TM节律的峰值明显提前,比2N小鼠早约4小时出现。总体而言,Ts65Dn小鼠活动亢进,其特定行为的日常模式与2N同窝小鼠有显著差异。为了控制Ts65Dn小鼠和2N小鼠视网膜退化的潜在混杂因素,我们进行了比较,发现2N小鼠和非视网膜退化的C57/129Sv小鼠的TM节律参数没有差异,这表明Ts65Dn小鼠异常的行为节律性可能不是由于视杆和视锥光感受器的缺失。这些结果为进一步研究DS患者睡眠-觉醒障碍的生理基础提供了一个起点。