循环时钟基因 Per1/Per2 缺陷诱导小鼠早期与年龄相关的运动功能下降
Yimei Fan1, Hui Luo1, Nana Zheng1
1Center for Sleep and Circadian Medicine, The Affiliated Brain Hospital, Guangzhou Medical University, Guangdong, China; Guangdong Engineering Technology Research Center for Translational Medicine of Mental Disorders, Guangdong, China; Key Laboratory of Sleep and Biological Rhythms of Guangdong Province, The Affiliated Brain Hospital, Guangzhou Medical University, Guangdong, China.
缺少昼夜钟基因Per1和Per2的小鼠随着年龄的增长显示出节律的破坏和运动技能的恶化. 循环节障碍在运动缺陷之前出现,突出显示了时钟基因对衰老运动功能的重要性.
科学领域:
- 时间生物学 时间生物学
- 神经科学是一个神经科学.
- 衰老研究研究 衰老研究
背景情况:
- 循环时钟基因Per1和Per2调节生物节奏.
- 对Per1/Per2缺乏对运动功能和衰老的影响尚不清楚.
研究的目的:
- 调查Per1/Per2双淘汰赛 (DKO) 对小鼠运动功能的年龄相关影响.
- 分析基因型 (Per1/Per2 DKO与野生类型) 和年龄之间的交互作用,对昼夜和运动行为.
主要方法:
- 轮子运行测试用于昼夜活动.
- 极点测试和旋转杆测试用于评估运动功能.
- 开放场地测试用于探索性行为评估.
- 基因型和年龄对昼夜和运动参数的影响的分析.
主要成果:
- 不管年龄,Per1/Per2 DKO小鼠表现出受光驱动的节律中断.
- 在DKO小鼠中,从2个月到9个月的年龄,运动功能显著下降.
- 缺少Per1/Per2主要影响平衡和协调,随着年龄的增长而恶化;仅仅年龄的影响是最小的.
- 在运动缺陷表现出来之前,年轻的DKO小鼠中显而易见的循环节障碍.
结论:
- 缺乏Per1/Per2会加剧与年龄相关的运动衰退.
- 循环时钟基因对于在衰老过程中维持运动功能和行为组织至关重要.
- 循环节障碍在运动缺陷之前发生,这表明存在因果关系.
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