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TG68,一种新型甲状腺激素受体-β激动剂,用于治疗非酒精性脂肪性肝病。

TG68, a Novel Thyroid Hormone Receptor-β Agonist for the Treatment of NAFLD.

机构信息

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.

出版信息

Int J Mol Sci. 2021 Dec 3;22(23):13105. doi: 10.3390/ijms222313105.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/254c/8657920/dd4643875b4d/ijms-22-13105-g001.jpg

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