Żełabowski Kacper, Petrov Wiktor, Wojtysiak Kacper, Ratka Zuzanna, Biedka Kamil, Wesołowski Michał, Fus Katarzyna, Ślebioda Dawid, Rusinek Malwina, Sterkowicz Maria, Radzka Izabela, Chłopaś-Konowałek Agnieszka
Scientific Society for Psychopharmacology, Department of Forensic Medicine, Wroclaw Medical University, 4 J. Mikulicza-Radeckiego Street, 50345 Wroclaw, Poland.
Department of Physiology and Pathophysiology, Division of Pathophysiology, Wroclaw Medical University, Chalubinskiego 10, 50368 Wroclaw, Poland.
Int J Mol Sci. 2025 Sep 6;26(17):8700. doi: 10.3390/ijms26178700.
The orexin (hypocretin) system plays a central role in regulating the sleep-wake cycle through two neuropeptides, orexin-A and orexin-B, which act on OX1R and OX2R receptors. Emerging evidence links heightened orexin signaling with the pathophysiology of chronic insomnia. This review outlines the neurobiology of the orexinergic system, compares the pharmacological profile of dual orexin receptor antagonists (DORAs) to traditional GABAergic hypnotics, and evaluates the clinical efficacy and safety of Suvorexant, Lemborexant, and Daridorexant. DORAs function by selectively dampening orexin-driven arousal, thereby facilitating sleep onset and maintenance without disrupting natural sleep architecture. Clinical trials have shown that these agents significantly reduce sleep latency and enhance sleep continuity, with a favorable side effect profile. Overall, DORAs represent a distinct and clinically advantageous option for insomnia treatment, with growing interest in their potential utility across mood, anxiety, and neurodegenerative disorders.
食欲素(下丘脑泌素)系统通过两种神经肽——食欲素-A和食欲素-B发挥核心作用,调节睡眠-觉醒周期,这两种神经肽作用于OX1R和OX2R受体。新出现的证据表明,食欲素信号增强与慢性失眠的病理生理学有关。本综述概述了食欲素能系统的神经生物学,比较了双重食欲素受体拮抗剂(DORAs)与传统GABA能催眠药的药理学特征,并评估了苏沃雷生、伦博雷生和达立雷生的临床疗效和安全性。DORAs通过选择性抑制食欲素驱动的觉醒发挥作用,从而促进睡眠开始和维持,而不会破坏自然睡眠结构。临床试验表明,这些药物能显著缩短睡眠潜伏期并增强睡眠连续性,且副作用较小。总体而言,DORAs是一种独特且具有临床优势的失眠治疗选择,人们对其在情绪、焦虑和神经退行性疾病中的潜在用途越来越感兴趣。