Fifel Karim, Vezoli Julien, Dzahini Kwamivi, Claustrat Bruno, Leviel Vincent, Kennedy Henry, Procyk Emmanuel, Dkhissi-Benyahya Ouria, Gronfier Claude, Cooper Howard M
Inserm, U846, Stem Cell and Brain Research Institute, Bron, France ; Université de Lyon, Lyon 1, UMR-S 846, Lyon, France.
PLoS One. 2014 Jan 23;9(1):e86240. doi: 10.1371/journal.pone.0086240. eCollection 2014.
Disturbances of the daily sleep/wake cycle are common non-motor symptoms of Parkinson's disease (PD). However, the impact of dopamine (DA) depletion on circadian rhythms in PD patients or non-human primate (NHP) models of the disorder have not been investigated. We evaluated alterations of circadian rhythms in NHP following MPTP lesion of the dopaminergic nigro-striatal system. DA degeneration was assessed by in vivo PET ([(11)C]-PE2I) and post-mortem TH and DAT quantification. In a light∶dark cycle, control and MPTP-treated NHP both exhibit rest-wake locomotor rhythms, although DA-depleted NHP show reduced amplitude, decreased stability and increased fragmentation. In all animals, 6-sulphatoxymelatonin peaks at night and cortisol in early morning. When the circadian system is challenged by exposure to constant light, controls retain locomotor rest-wake and hormonal rhythms that free-run with stable phase relationships whereas in the DA-depleted NHP, locomotor rhythms are severely disturbed or completely abolished. The amplitude and phase relations of hormonal rhythms nevertheless remain unaltered. Use of a light-dark masking paradigm shows that expression of daily rest-wake activity in MPTP monkeys requires the stimulatory and inhibitory effects of light and darkness. These results suggest that following DA lesion, the central clock in the SCN remains intact but, in the absence of environmental timing cues, is unable to drive downstream rhythmic processes of striatal clock gene and dopaminergic functions that control locomotor output. These findings suggest that the circadian component of the sleep-wake disturbances in PD is more profoundly affected than previously assumed.
日常睡眠/觉醒周期紊乱是帕金森病(PD)常见的非运动症状。然而,多巴胺(DA)耗竭对PD患者或该疾病的非人类灵长类动物(NHP)模型昼夜节律的影响尚未得到研究。我们评估了多巴胺能黑质纹状体系统经MPTP损伤后NHP昼夜节律的改变。通过体内PET([(11)C]-PE2I)以及死后TH和DAT定量评估DA变性。在明暗周期中,对照和MPTP处理的NHP均表现出休息-觉醒运动节律,尽管DA耗竭的NHP表现出振幅降低、稳定性下降和碎片化增加。在所有动物中,6-硫酸氧褪黑素在夜间达到峰值,皮质醇在清晨达到峰值。当昼夜节律系统受到持续光照的挑战时,对照组保持运动休息-觉醒和激素节律,这些节律以稳定的相位关系自由运行,而在DA耗竭的NHP中,运动节律受到严重干扰或完全消失。然而,激素节律的振幅和相位关系保持不变。使用明暗掩蔽范式表明,MPTP猴子日常休息-觉醒活动的表达需要光和暗的刺激和抑制作用。这些结果表明,DA损伤后,SCN中的中央时钟保持完整,但在没有环境时间线索的情况下,无法驱动控制运动输出的纹状体时钟基因和多巴胺能功能的下游节律性过程。这些发现表明,PD中睡眠-觉醒障碍的昼夜节律成分比以前认为的受到更深刻的影响。