Pupo André S, Duarte Diego A, Lima Vanessa, Teixeira Larissa B, Parreiras-E-Silva Lucas T, Costa-Neto Claudio M
Department of Pharmacology, Instituto de Biociências, UNESP, Botucatu, SP, Brazil.
Department of Biochemistry and Immunology, Faculty of Medicine at Ribeirão Preto, University of São Paulo, 14049-900 Ribeirão Preto, SP, Brazil.
Pharmacol Res. 2016 Oct;112:49-57. doi: 10.1016/j.phrs.2016.01.031. Epub 2016 Feb 2.
G protein-coupled receptors (GPCRs) are the most important targets for drug discovery and not surprisingly ∼40% of all drugs currently in the market act on these receptors. Currently, one of the most active areas in GPCRs signaling is biased agonism, a phenomenon that occurs when a given ligand is able to preferentially activate one (or some) of the possible signaling pathways. In this review, we highlight the most recent findings about biased agonism, including an extension of this concept to intracellular signaling, allosterism, strategies for assessment and interpretation, and perspectives of therapeutic applications for biased agonists.
G蛋白偶联受体(GPCRs)是药物研发最重要的靶点,目前市场上约40%的药物作用于这些受体也就不足为奇了。目前,GPCRs信号传导中最活跃的领域之一是偏向性激动作用,即当给定配体能够优先激活一种(或某些)可能的信号传导途径时发生的现象。在本综述中,我们重点介绍了关于偏向性激动作用的最新发现,包括这一概念在细胞内信号传导、别构作用方面的扩展,评估和解释策略,以及偏向性激动剂的治疗应用前景。