Cytokines in sleep regulation

James M. Krueger, Satoshi Takahashi, Levente Kapás, Sebastian Bredow, Rachida Roky, Jidong Fang, Rachael Floyd, Kathryn B. Renegar, Nandita Guha-Thakurta, Sergei Novitsky, Ferenc Obál Jr
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引用次数: 102

Abstract

The central thesis of this essay is that the cytokine network in brain is a key element in the humoral regulation of sleep responses to infection and in the physiological regulation of sleep. We hypothesize that many cytokines, their cellular receptors, soluble receptors, and endogenous antagonists are involved in physiological sleep regulation. The expressions of some cytokines are greatly amplified by microbial challenge. This excess cytokine production during infection induces sleep responses. The excessive sleep and wakefulness that occur at different times during the course of the infectious process result from dynamic changes in various cytokines that occur during the host's response to infectious challenge. Removal of any one somnogenic cytokine inhibits normal sleep, alters the cytokine network by changing the cytokine mix, but does not completely disrupt sleep due to the redundant nature of the cytokine network. The cytokine network operates in a paracrine/autocrine fashion and is responsive to neuronal use. Finally, cytokines elicit their somnogenic actions via endocrine and neurotransmitter systems as well as having direct effects on neurons and glia. Evidence in support of these postulates is reviewed in this essay.

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睡眠调节中的细胞因子
本文的中心论点是,大脑细胞因子网络在感染对睡眠反应的体液调节和睡眠的生理调节中起着关键作用。我们假设许多细胞因子、它们的细胞受体、可溶性受体和内源性拮抗剂都参与了生理睡眠调节。一些细胞因子的表达在微生物挑战下被大大放大。感染期间过量的细胞因子产生会引起睡眠反应。在感染过程中不同时间发生的过度睡眠和清醒是由于宿主在应对感染挑战过程中发生的各种细胞因子的动态变化。去除任何一种促睡眠细胞因子会抑制正常睡眠,通过改变细胞因子的组合来改变细胞因子网络,但由于细胞因子网络的冗余性,不会完全破坏睡眠。细胞因子网络以旁分泌/自分泌方式运作,并对神经元的使用作出反应。最后,细胞因子通过内分泌和神经递质系统引发促睡作用,并直接作用于神经元和神经胶质细胞。本文回顾了支持这些假设的证据。
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