Department of Anesthesiology, Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110, United States.
Center for Clinical Pharmacology, St. Louis College of Pharmacology and Washington University in St. Louis, St. Louis, Missouri 63110, United States.
Biochemistry. 2021 May 11;60(18):1401-1412. doi: 10.1021/acs.biochem.0c00644. Epub 2020 Nov 13.
Pain is an essential protective mechanism that the body uses to alert or prevent further damage. Pain sensation is a complex event involving perception, transmission, processing, and response. Neurons at different levels (peripheral, spinal cord, and brain) are responsible for these pro- or antinociceptive activities to ensure an appropriate response to external stimuli. The terminals of these neurons, both in the peripheral endings and in the synapses, are equipped with G protein-coupled receptors (GPCRs), voltage- and ligand-gated ion channels that sense structurally diverse stimuli and inhibitors of neuronal activity. This review will focus on the largest class of sensory proteins, the GPCRs, as they are distributed throughout ascending and descending neurons and regulate activity at each step during pain transmission. GPCR activation also directly or indirectly controls the function of co-localized ion channels. The levels and types of some GPCRs are significantly altered in different pain models, especially chronic pain states, emphasizing that these molecules could be new targets for therapeutic intervention in chronic pain.
疼痛是身体用来发出警告或防止进一步损伤的一种重要保护机制。疼痛感觉是一个涉及感知、传递、处理和反应的复杂事件。不同水平的神经元(外周、脊髓和大脑)负责这些促进或抗伤害活动,以确保对外界刺激做出适当的反应。这些神经元的末梢,无论是在外周末梢还是在突触中,都配备有 G 蛋白偶联受体(GPCR)、电压门控和配体门控离子通道,它们可以感知结构多样的刺激和神经元活性的抑制剂。这篇综述将集中讨论最大的一类感觉蛋白,即 GPCR,因为它们分布在上升和下降神经元中,并调节疼痛传递过程中的每一个步骤的活动。GPCR 的激活也直接或间接控制着共定位离子通道的功能。在不同的疼痛模型中,特别是慢性疼痛状态下,一些 GPCR 的水平和类型会发生显著改变,这强调了这些分子可能是慢性疼痛治疗干预的新靶点。