Guangdong Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510006, China.
Health Science Centre, School of Pharmaceutical Sciences, Shenzhen University, Shenzhen 518060, China.
Int J Mol Sci. 2022 Jan 20;23(3):1102. doi: 10.3390/ijms23031102.
Non-alcoholic fatty liver disease (NAFLD) is the fastest-growing liver disease in the world. Despite targeted agents which are needed to provide permanent benefits for patients with NAFLD, no drugs have been approved to treat NASH. Thyroid hormone is an important signaling molecule to maintain normal metabolism, and in vivo and vitro studies have shown that regulation of the 3,5,3'-triiodothyronine (T3)/ thyroid hormone receptor (TR) axis is beneficial not only for metabolic symptoms but also for the improvement of NAFLD and even for the repair of liver injury. However, the non-selective regulation of T3 to TR subtypes (TRα/TRβ) could cause unacceptable side effects represented by cardiotoxicity. To avoid deleterious effects, TRβ-selective thyromimetics were developed for NASH studies in recent decades. Herein, we will review the development of thyroid hormones and synthetic thyromimetics based on TR selectivity for NAFLD, and analyze the role of TR-targeted drugs for the treatment of NAFLD in the future.
非酒精性脂肪性肝病(NAFLD)是世界上增长最快的肝病。尽管需要有针对性的药物为 NAFLD 患者提供永久的益处,但尚无药物被批准用于治疗 NASH。甲状腺激素是维持正常代谢的重要信号分子,体内和体外研究表明,调节 3,5,3'-三碘甲状腺原氨酸(T3)/甲状腺激素受体(TR)轴不仅对代谢症状有益,而且对改善 NAFLD 甚至对肝损伤的修复也有益。然而,T3 对 TR 亚型(TRα/TRβ)的非选择性调节可能会导致以心脏毒性为代表的不可接受的副作用。为了避免有害影响,近年来已开发出 TR 选择性甲状腺素类似物用于 NASH 研究。在此,我们将回顾基于 TR 选择性的甲状腺激素和合成甲状腺素类似物在 NAFLD 方面的发展,并分析 TR 靶向药物在未来治疗 NAFLD 的作用。