Department of Molecular Therapeutics, The Scripps Research Institute, Scripps Florida, Jupiter, FL 33458, USA.
Department of Molecular Therapeutics, The Scripps Research Institute, Scripps Florida, Jupiter, FL 33458, USA.
Cell Metab. 2014 Feb 4;19(2):193-208. doi: 10.1016/j.cmet.2013.12.009. Epub 2014 Jan 16.
Nuclear receptors (NRs) play central roles in metabolic syndrome, making them attractive drug targets despite the challenge of achieving functional selectivity. For instance, members of the thiazolidinedione class of insulin sensitizers offer robust efficacy but have been limited due to adverse effects linked to activation of genes not involved in insulin sensitization. Studies reviewed here provide strategies for targeting subsets of PPARγ target genes, enabling development of next-generation modulators with improved therapeutic index. Additionally, emerging evidence suggests that targeting the NRs ROR and Rev-erb holds promise for treating metabolic syndrome based on their involvement in circadian rhythm and metabolism.
核受体 (NRs) 在代谢综合征中发挥着核心作用,使它们成为有吸引力的药物靶点,尽管实现功能选择性具有挑战性。例如,噻唑烷二酮类胰岛素增敏剂具有强大的疗效,但由于与胰岛素增敏无关的基因激活相关的不良反应而受到限制。本文综述了针对 PPARγ 靶基因亚群的策略,为开发具有改善治疗指数的新一代调节剂提供了可能。此外,新出现的证据表明,基于其在昼夜节律和代谢中的参与,靶向核受体 ROR 和 Rev-erb 有望治疗代谢综合征。