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首页> 外文期刊>The European Journal of Neuroscience >Developmental divergence of sleep-wake patterns in orexin knockout and wild-type mice.
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Developmental divergence of sleep-wake patterns in orexin knockout and wild-type mice.

机译:在orexin基因敲除小鼠和野生型小鼠中睡眠-觉醒模式的发育差异。

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摘要

Narcolepsy, a disorder characterized by fragmented bouts of sleep and wakefulness during the day and night as well as cataplexy, has been linked in humans and nonhuman animals to the functional integrity of the orexinergic system. Adult orexin knockout mice and dogs with a mutation of the orexin receptor exhibit symptoms that mirror those seen in narcoleptic humans. As with narcolepsy, infant sleep-wake cycles in humans and rats are highly fragmented, with consolidated bouts of sleep and wakefulness developing gradually. Based on these common features of narcoleptics and infants, we hypothesized that the development of sleep-wake fragmentation in orexin knockout mice would be expressed as a developmental divergence between knockouts and wild-types, with the knockouts lagging behind the wild-types. We tested this hypothesis by recording the sleep-wake patterns of infant orexin knockout and wild-type mice across the first three postnatal weeks. Both knockouts and wild-types exhibited age-dependent, and therefore orexin-independent, quantitative and qualitative changes in sleep-wake patterning. At 3 weeks of age, however, by which time the sleep and wake bouts of the wild-types had consolidated further, the knockouts lagged behind the wild-types and exhibited significantly more bout fragmentation. These findings suggest the possibility that the fragmentation of behavioural states that characterizes narcolepsy in adults reflects reversion back toward the more fragmented sleep-wake patterns that characterize infancy.
机译:发作性睡病是一种以昼夜不停的睡眠和清醒以及瘫痪为特征的疾病,已在人类和非人类动物中与食欲能系统的功能完整性相关联。具有orexin受体突变的成年orexin基因敲除小鼠和狗表现出与麻醉性人类相似的症状。与发作性睡病一样,人类和大鼠的婴儿觉醒周期高度分散,逐渐形成巩固的睡眠和清醒周期。基于麻醉药和婴儿的这些共同特征,我们假设在orexin基因敲除小鼠中睡眠觉醒破碎的发展将表现为基因敲除与野生型之间的发育差异,基因敲除落后于野生型。我们通过在出生后前三周记录婴儿orexin基因敲除小鼠和野生型小鼠的睡眠-觉醒模式来检验该假设。基因敲除和野生型都表现出年龄依赖性,因此在睡眠-觉醒模式中与食欲素无关,在数量和质量上都有变化。然而,在3周龄时,野生型的睡眠和唤醒回合进一步巩固,敲除基因落后于野生型,并且表现出明显更多的回合碎裂。这些发现表明,表征成年发作性睡病的行为状态的分裂反映了向着更分裂的,表征婴儿的睡眠-觉醒模式的回归。

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