Foster Daniel J, Conn P Jeffrey
Department of Pharmacology, Vanderbilt University, Nashville, TN 37232, USA; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232, USA.
Department of Pharmacology, Vanderbilt University, Nashville, TN 37232, USA; Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University, Nashville, TN 37232, USA.
Neuron. 2017 May 3;94(3):431-446. doi: 10.1016/j.neuron.2017.03.016.
G-protein-coupled receptors (GPCRs) play critical roles in regulating brain function. Recent advances have greatly expanded our understanding of these receptors as complex signaling machines that can adopt numerous conformations and modulate multiple downstream signaling pathways. While agonists and antagonists have traditionally been pursued to target GPCRs, allosteric modulators provide several mechanistic advantages, including the ability to distinguish between closely related receptor subtypes. Recently, the discovery of allosteric ligands that confer bias and modulate some, but not all, of a given receptor's downstream signaling pathways can provide pharmacological modulation of brain circuitry with remarkable precision. In addition, allosteric modulators with unprecedented specificity have been developed that can differentiate between subpopulations of a given receptor subtype based on the receptor's dimerization state. These advances are not only providing insight into the biological roles of specific receptor populations, but hold great promise for treating numerous CNS disorders.
G蛋白偶联受体(GPCRs)在调节脑功能中发挥着关键作用。最近的进展极大地扩展了我们对这些受体的理解,它们是复杂的信号传导机器,能够呈现多种构象并调节多个下游信号通路。虽然传统上一直致力于寻找激动剂和拮抗剂来靶向GPCRs,但变构调节剂具有多种机制优势,包括能够区分密切相关的受体亚型。最近,发现了赋予偏向性并调节给定受体部分而非全部下游信号通路的变构配体,这可以以显著的精度对脑回路进行药理学调节。此外,已经开发出具有前所未有的特异性的变构调节剂,它们可以根据受体的二聚化状态区分给定受体亚型的亚群。这些进展不仅有助于深入了解特定受体群体的生物学作用,而且在治疗多种中枢神经系统疾病方面具有巨大潜力。