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食欲素神经元回路:在睡眠和觉醒调节中的作用。

Orexin neuronal circuitry: role in the regulation of sleep and wakefulness.

作者信息

Ohno Kousaku, Sakurai Takeshi

机构信息

Department of Pharmacology, Institute of Basic Medical Science, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.

出版信息

Front Neuroendocrinol. 2008 Jan;29(1):70-87. doi: 10.1016/j.yfrne.2007.08.001. Epub 2007 Aug 29.

Abstract

Orexin A and orexin B were initially identified as endogenous ligands for two orphan G protein-coupled receptors [104]. They were initially recognized as regulators of feeding behavior in view of their exclusive production in the lateral hypothalamic area (LHA), a region known as the feeding center, and their pharmacological activity [104,30,49,107]. Subsequently, the finding that orexin deficiency causes narcolepsy in humans and animals suggested that these hypothalamic neuropeptides play a critical role in regulating sleep/wake cycle [22,46,71,95,117]. These peptides activate waking-active monoaminergic and cholinergic neurons in the hypothalamus/brain stem regions to maintain a long, consolidated awake period. Recent studies on efferent and afferent systems of orexin neurons, and phenotypic characterization of genetically modified mice in the orexin system further suggested roles of orexin in the coordination of emotion, energy homeostasis, reward system, and arousal [3,80,106,137]. A link between the limbic system and orexin neurons might be important for increasing vigilance during emotional stimuli. Orexin neurons are also regulated by peripheral metabolic cues, including ghrelin, leptin, and glucose, suggesting that they might have important roles as a link between energy homeostasis and vigilance states [137]. Recent research has also implicated orexins in reward systems and the mechanisms of drug addiction [13,48,91]. These observations suggest that orexin neurons sense the outer and inner environment of the body, and maintain proper wakefulness of animals for survival. This review discusses the mechanism by which orexins maintain sleep/wakefulness states, and how this mechanism relates to other systems that regulate emotion, reward, and energy homeostasis.

摘要

食欲素A和食欲素B最初被鉴定为两种孤儿G蛋白偶联受体的内源性配体[104]。鉴于它们仅在下丘脑外侧区(LHA)产生,该区域被称为进食中枢,以及它们的药理活性,它们最初被认为是进食行为的调节因子[104,30,49,107]。随后,食欲素缺乏会导致人类和动物发作性睡病这一发现表明,这些下丘脑神经肽在调节睡眠/觉醒周期中起关键作用[22,46,71,95,117]。这些肽激活下丘脑/脑干区域中促进觉醒的单胺能和胆碱能神经元,以维持长时间的、巩固的清醒期。最近对食欲素神经元的传出和传入系统的研究,以及对食欲素系统中基因改造小鼠的表型特征分析,进一步表明食欲素在情绪协调、能量稳态、奖赏系统和觉醒中发挥作用[3,80,106,137]。边缘系统与食欲素神经元之间的联系对于在情绪刺激期间提高警觉性可能很重要。食欲素神经元也受到外周代谢信号的调节,包括胃饥饿素、瘦素和葡萄糖,这表明它们可能作为能量稳态和警觉状态之间的联系发挥重要作用[137]。最近的研究还表明食欲素与奖赏系统和药物成瘾机制有关[13,48,91]。这些观察结果表明,食欲素神经元感知身体的外部和内部环境,并维持动物适当的清醒以利于生存。本综述讨论了食欲素维持睡眠/觉醒状态的机制,以及该机制如何与调节情绪、奖赏和能量稳态的其他系统相关。

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