Department of Pharmaceutical and Pharmacological Sciences, University of Padua, Padua, Italy.
Department of Biomedical Sciences, University of Padua, Padua, Italy.
J Pineal Res. 2024 Oct;76(7):e13011. doi: 10.1111/jpi.13011.
Sleep, constituting approximately one-third of the human lifespan, is a crucial physiological process essential for physical and mental well-being. Normal sleep consists of an orderly progression through wakefulness, non-rapid eye movement (NREM) sleep, and rapid eye movement (REM) sleep, all of which are tightly regulated. Melatonin, often referred to as the "hormone of sleep," plays a pivotal role as a regulator of the sleep/wake cycle and exerts its effects through high-affinity G-protein coupled receptors known as MT1 and MT2. Selective modulation of these receptors presents a promising therapeutic avenue for sleep disorders. This review examines research on the multifaceted role of melatonin in sleep regulation, focusing on selective ligands targeting MT1 and MT2 receptors, as well as studies involving MT1 and MT2 knockout mice. Contrary to common beliefs, growing evidence suggests that melatonin, through MT1 and MT2 receptors, might not only influence circadian aspects of sleep but likely, also modulate the homeostatic process of sleep and sleep architecture, or could be the molecule linking the homeostatic and circadian regulation of sleep. Furthermore, the distinct brain localization of MT1 and MT2 receptors, with MT1 receptors primarily regulating REM sleep and MT2 receptors regulating NREM sleep, is discussed. Collectively, sleep regulation extends beyond the circulating levels and circadian peak of melatonin; it also critically involves the expression, molecular activation, and regulatory functions of MT1 and MT2 receptors across various brain regions and nuclei involved in the regulation of sleep. This research underscores the importance of ongoing investigation into the selective roles of MT1 and MT2 receptors in sleep. Such research efforts are expected to pave the way for the development of targeted MT1 or MT2 receptors ligands, thereby optimizing therapeutic interventions for sleep disorders.
睡眠占据人类生命的三分之一,是身心健康所必需的重要生理过程。正常睡眠由清醒、非快速眼动 (NREM) 睡眠和快速眼动 (REM) 睡眠有序地进行,所有这些都受到严格的调节。褪黑素常被称为“睡眠激素”,作为睡眠/觉醒周期的调节剂发挥着关键作用,通过高亲和力 G 蛋白偶联受体 MT1 和 MT2 发挥作用。这些受体的选择性调节为睡眠障碍的治疗提供了有前途的途径。本综述研究了褪黑素在睡眠调节中的多方面作用,重点关注靶向 MT1 和 MT2 受体的选择性配体,以及涉及 MT1 和 MT2 敲除小鼠的研究。与普遍看法相反,越来越多的证据表明,褪黑素通过 MT1 和 MT2 受体不仅可能影响睡眠的昼夜节律方面,而且可能调节睡眠的稳态过程和睡眠结构,或者可能是将睡眠的稳态和昼夜节律调节联系起来的分子。此外,还讨论了 MT1 和 MT2 受体在大脑中的不同定位,MT1 受体主要调节 REM 睡眠,MT2 受体调节 NREM 睡眠。总的来说,睡眠调节不仅超越了褪黑素的循环水平和昼夜节律高峰,还涉及 MT1 和 MT2 受体在参与睡眠调节的各种大脑区域和核团中的表达、分子激活和调节功能。这项研究强调了对 MT1 和 MT2 受体在睡眠中的选择性作用进行持续研究的重要性。这些研究工作有望为开发靶向 MT1 或 MT2 受体的配体铺平道路,从而优化睡眠障碍的治疗干预措施。