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首页> 外文期刊>PLoS Biology >Melanopsin as a Sleep Modulator: Circadian Gating of the Direct Effects of Light on Sleep and Altered Sleep Homeostasis in Opn4?/? Mice
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Melanopsin as a Sleep Modulator: Circadian Gating of the Direct Effects of Light on Sleep and Altered Sleep Homeostasis in Opn4?/? Mice

机译:黑素作为睡眠调节剂:昼夜控制光对睡眠的直接影响以及Opn4?/?中睡眠稳态的改变。老鼠

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摘要

Light influences sleep and alertness either indirectly through a well-characterized circadian pathway or directly through yet poorly understood mechanisms. Melanopsin (Opn4) is a retinal photopigment crucial for conveying nonvisual light information to the brain. Through extensive characterization of sleep and the electrocorticogram (ECoG) in melanopsin-deficient (Opn4?/?) mice under various light–dark (LD) schedules, we assessed the role of melanopsin in mediating the effects of light on sleep and ECoG activity. In control mice, a light pulse given during the habitual dark period readily induced sleep, whereas a dark pulse given during the habitual light period induced waking with pronounced theta (7–10 Hz) and gamma (40–70 Hz) activity, the ECoG correlates of alertness. In contrast, light failed to induce sleep in Opn4?/? mice, and the dark-pulse-induced increase in theta and gamma activity was delayed. A 24-h recording under a LD 1-h∶1-h schedule revealed that the failure to respond to light in Opn4?/? mice was restricted to the subjective dark period. Light induced c-Fos immunoreactivity in the suprachiasmatic nuclei (SCN) and in sleep-active ventrolateral preoptic (VLPO) neurons was importantly reduced in Opn4?/? mice, implicating both sleep-regulatory structures in the melanopsin-mediated effects of light. In addition to these acute light effects, Opn4?/? mice slept 1 h less during the 12-h light period of a LD 12∶12 schedule owing to a lengthening of waking bouts. Despite this reduction in sleep time, ECoG delta power, a marker of sleep need, was decreased in Opn4?/? mice for most of the (subjective) dark period. Delta power reached after a 6-h sleep deprivation was similarly reduced in Opn4?/? mice. In mice, melanopsin's contribution to the direct effects of light on sleep is limited to the dark or active period, suggesting that at this circadian phase, melanopsin compensates for circadian variations in the photo sensitivity of other light-encoding pathways such as rod and cones. Our study, furthermore, demonstrates that lack of melanopsin alters sleep homeostasis. These findings call for a reevaluation of the role of light on mammalian physiology and behavior.
机译:光线会通过良好的昼夜节律途径间接影响睡眠和机敏性,或者直接通过尚未充分了解的机制直接影响睡眠和机敏性。黑素(Opn4)是视网膜色素沉着,对于将非视觉光信息传递到大脑至关重要。通过在各种明暗(LD)计划下对缺乏黑素视蛋白(Opn4?/?)的小鼠的睡眠和脑电图(ECoG)进行广泛的表征,我们评估了黑素在介导光对睡眠和ECoG活性的影响中的作用。在对照小鼠中,在习惯性黑暗时期发出的光脉冲容易诱发睡眠,而在惯性黑暗时期发出的暗脉冲则以明显的θ(7–10 Hz)和γ(40–70 Hz)活动,即ECoG唤醒。警觉性相关。相反,光不能诱导Opn4?/?中的睡眠。小鼠,并且暗脉冲诱导的theta和γ活性增加被延迟。根据LD 1-h1:1-h时间表进行的24小时记录显示,Opn4?/?中对光的响应失败。小鼠仅限于主观黑暗期。 Opn4α/β重要地降低了光诱导的视交叉上核(SCN)和睡眠活动性腹侧前视神经(VLPO)神经元中的c-Fos免疫反应性。小鼠,这牵涉到黑色素介导的光的两种睡眠调节结构。除了这些急性光效应外,Opn4?/?还可以。在LD 121:12的12小时光照期间,小鼠的睡眠时间减少了1小时,这是因为醒来的发作时间延长了。尽管减少了睡眠时间,但Opn4α/β降低了ECoGδ功率(睡眠需求的标志)。小鼠在大部分(主观)黑暗时期都处于活动状态。在Opn4?/?中,剥夺6小时睡眠后达到的Delta功率也降低了。老鼠。在小鼠中,黑色素对光对睡眠的直接影响的作用仅限于黑暗或活跃时期,这表明在这个昼夜节律阶段,黑色素可以补偿其他光编码途径(如杆和视锥细胞)的光敏性昼夜节律变化。此外,我们的研究表明,缺乏黑素能改变睡眠稳态。这些发现要求重新评估光对哺乳动物生理和行为的作用。

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