Wang Yutong, Fu Su, Mao Jian, Cui Kun, Jiang Hong
Beijing Life Science Academy, Beijing, China.
Department of Neurobiology, School of Basic Medical Sciences, Neuroscience Research Institute, Peking University, Beijing, China.
Front Neurosci. 2025 Aug 25;19:1638270. doi: 10.3389/fnins.2025.1638270. eCollection 2025.
Hypocretin, also known as orexin, is a hypothalamic neuropeptide that regulates essential physiological processes including arousal, energy metabolism, feeding behavior, and emotional states. Through widespread projections and two G-protein-coupled receptors-HCRT-1R and HCRT-2R-the hypocretin system exerts diverse modulatory effects across the central nervous system. The role of hypocretin in maintaining wakefulness is well established, particularly in narcolepsy type 1 (NT1), where loss of hypocretin neurons leads to excessive daytime sleepiness and cataplexy. However, the mechanisms by which hypocretin stabilizes transitions between sleep stages remain incompletely understood. Additionally, while hypocretin integrates metabolic signals such as glucose, leptin, and ghrelin to promote feeding and energy expenditure, NT1 patients paradoxically experience weight gain despite reduced caloric intake-highlighting unresolved questions about hypocretin's role in energy homeostasis. In the affective domain, preclinical studies suggest hypocretin enhances stress resilience and modulates anxiety- and depression-related behaviors. Yet, human data remain inconsistent, in part due to methodological variability and the limited availability of cerebrospinal fluid sampling to accurately assess central hypocretin function. Therapeutically, the hypocretin system is a promising target across several domains. Dual hypocretin receptor antagonists (DORAs), such as suvorexant and daridorexant, are clinically approved for insomnia. Selective HCRT-2R agonists-including TAK-861 and ALKS-2680-are in clinical trials for NT1 and show encouraging results. Additionally, HCRT-2R antagonists like seltorexant are being explored for major depressive disorder. This review will highlight the anatomical distribution, receptor mechanisms, and physiological functions of the hypocretin system. It will also focus to discuss its role in narcolepsy, metabolic regulation, and mood disorders, while addressing key challenges and open questions that must be resolved to fully harness hypocretin's therapeutic potential.
下丘脑分泌素,也被称为食欲素,是一种下丘脑神经肽,可调节包括觉醒、能量代谢、进食行为和情绪状态在内的基本生理过程。通过广泛的投射以及两种G蛋白偶联受体——HCRT - 1R和HCRT - 2R,下丘脑分泌素系统在中枢神经系统中发挥多种调节作用。下丘脑分泌素在维持清醒状态中的作用已得到充分证实,尤其是在1型发作性睡病(NT1)中,下丘脑分泌素神经元的缺失会导致日间过度嗜睡和猝倒。然而,下丘脑分泌素稳定睡眠阶段转换的机制仍未完全明确。此外,虽然下丘脑分泌素整合葡萄糖、瘦素和胃饥饿素等代谢信号以促进进食和能量消耗,但NT1患者尽管热量摄入减少却反而体重增加——这凸显了关于下丘脑分泌素在能量稳态中作用的尚未解决的问题。在情感领域,临床前研究表明下丘脑分泌素可增强应激恢复力并调节与焦虑和抑郁相关的行为。然而,人类数据仍然不一致,部分原因是方法的变异性以及用于准确评估中枢下丘脑分泌素功能的脑脊液采样的有限可用性。在治疗方面,下丘脑分泌素系统在多个领域都是一个有前景的靶点。双重下丘脑分泌素受体拮抗剂(DORAs),如苏沃雷生和达利雷生,已被临床批准用于治疗失眠。选择性HCRT - 2R激动剂——包括TAK - 861和ALKS - 2680——正在进行NT1的临床试验,并显示出令人鼓舞的结果。此外,像塞托雷生这样的HCRT - 2R拮抗剂正在被探索用于治疗重度抑郁症。本综述将重点介绍下丘脑分泌素系统的解剖分布、受体机制和生理功能。它还将着重讨论其在发作性睡病、代谢调节和情绪障碍中的作用,同时解决充分发挥下丘脑分泌素治疗潜力必须解决的关键挑战和悬而未决的问题。