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A Neuronal Hub Binding Sleep Initiation and Body Cooling in Response to a Warm External Stimulus

机译:响应于温暖的外部刺激,神经元轮毂结合睡眠起始和体冷却

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Mammals, including humans, prepare for sleep by nesting and/or curling up, creating microclimates of skin warmth. To address whether external warmth induces sleep through defined circuitry, we used c-Fos-dependent activity tagging, which captures populations of activated cells and allows them to be reactivated to test their physiological role. External warming tagged two principal groups of neurons in the median preoptic (MnPO)/medial preoptic (MPO) hypothalamic area. GABA neurons located mainly in MPO produced non-rapid eye movement (NREM) sleep but no body temperature decrease. Nitrergic-glutamatergic neurons in MnPO-MPO induced both body cooling and NREM sleep. This circuitry explains how skin warming induces sleep and why the maximal rate of core body cooling positively correlates with sleep onset. Thus, the pathways that promote NREM sleep, reduced energy expenditure, and body cooling are inextricably linked, commanded by the same neurons. This implies that one function of NREM sleep is to lower brain temperature and/or conserve energy.
机译:包括人类在内的哺乳动物,通过嵌套和/或卷曲准备睡眠,从而创造皮肤温暖的微观亚麻。为了解决外部温暖诱导睡眠通过定义电路,我们使用了C-FOS依赖性活动标记,其捕获活性细胞的群体,并允许它们重新激活以测试其生理作用。外部变暖标记在中位数(MNPO)/内侧次丘脑区域中的两个主要神经元组。 GABA神经元主要位于MPO生产的非快速眼球运动(NREM)睡眠,但没有体温降低。 MNPO-MPO中的Nitrergic-谷氨酸神经元诱导身体冷却和NREM睡眠。该电路介绍了皮肤变暖如何诱导睡眠以及为什么核心体冷却的最大速率与睡眠发作呈正相关。因此,促进NREM睡眠,降低能量消耗和体冷却的途径是密不可分的,由同一神经元命令。这意味着NREM睡眠的一个功能是降低脑温度和/或节能。

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