Unit of Oncology and Molecular Pathology, Department of Biomedical Sciences, University of Cagliari, 09042 Monserrato, Italy.
Department of Pharmacy, University of Pisa, 56126 Pisa, Italy.
Int J Mol Sci. 2021 Dec 3;22(23):13105. doi: 10.3390/ijms222313105.
Activation of thyroid hormone receptor β (THRβ) has shown beneficial effects on metabolic alterations, including non-alcoholic fatty liver disease (NAFLD). Here, we investigated the effect of TG68, a novel THRβ agonist, on fatty liver accumulation and liver injury in mice fed a high-fat diet (HFD). C57BL/6 mice fed HFD for 17 or 18 weeks, a time when all mice developed massive steatohepatitis, were then given TG68 at a dose of 9.35 or 2.8 mg/kg for 2 or 3 weeks, respectively. As a reference compound, the same treatment was adopted using equimolar doses of MGL-3196, a selective THRβ agonist currently in clinical phase III. The results showed that treatment with TG68 led to a reduction in liver weight, hepatic steatosis, serum transaminases, and circulating triglycerides. qRT-PCR analyses demonstrated activation of THRβ, as confirmed by increased levels of and , and changes in lipid metabolism, as revealed by increased expression of and . The present results showed that this novel THRβ agonist exerts an anti-steatogenic effect coupled with amelioration of liver injury in the absence of extra-hepatic side effects, suggesting that TG68 may represent a useful tool for the treatment of NAFLD.
甲状腺激素受体 β(THRβ)的激活已显示出对代谢改变的有益影响,包括非酒精性脂肪性肝病(NAFLD)。在这里,我们研究了新型 THRβ激动剂 TG68 对高脂肪饮食(HFD)喂养的小鼠脂肪肝蓄积和肝损伤的影响。C57BL/6 小鼠用 HFD 喂养 17 或 18 周,此时所有小鼠均发生大量脂肪性肝炎,然后分别给予 TG68 剂量为 9.35 或 2.8 mg/kg,持续 2 或 3 周。作为参考化合物,采用相同的治疗方法,用目前处于临床三期的选择性 THRβ激动剂 MGL-3196 的等摩尔剂量进行治疗。结果表明,TG68 治疗可降低肝重、肝脂肪变性、血清转氨酶和循环甘油三酯。qRT-PCR 分析表明 THRβ被激活,这通过 水平的增加得到证实,并且脂质代谢发生变化,表现为 和 的表达增加。本研究结果表明,这种新型 THRβ激动剂在没有肝外副作用的情况下具有抗脂肪生成作用,并改善肝损伤,提示 TG68 可能是治疗 NAFLD 的有用工具。