Chen Yu-Jun, Song Hai-Yan, Zhang Zi-Wei, Chen Qian, Tang Zhi-Peng, Gu Ming
Institute of Digestive Disease, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Front Pharmacol. 2021 Jul 30;12:711763. doi: 10.3389/fphar.2021.711763. eCollection 2021.
Chinese vine tea can improve glucose and lipid metabolic disorders. However, its protective effects in non-alcoholic steatohepatitis (NASH) and its underlying molecular mechanisms remain unclear. Liver X receptor α (LXRα) inhibition and adenosine monophosphate-(AMP)-activated protein kinase (AMPK) activation can enhance control of NASH. AMPK activators have also been shown to inactivate LXRα. Here, the anti-NASH effects of vine tea extract (VTE) dosed at 1 g.100 g diet were investigated using NASH mice challenged with a methionine and choline-deficient l-amino acid diet (MCDD) and a high-fat diet (HFD). Pharmacological mechanisms of VTE were explored using TUNEL staining, AMPK inhibition, Western blot, reporter assays, qRT-PCR analyses, and immunofluorescence. VTE treatment improved fatty liver in HFD-induced mice, while it alleviated the progression of NASH including protecting against liver lipid accumulation, steatosis, endoplasmic reticulum stress, apoptosis, inflammation, and functional injury in MCDD-fed mice. VTE reduced the action of hepatic lipogenic genes, F4/80, pro-inflammatory cytokines, CHOP, and cleaved Caspase-3 expression, while promoting expression of fatty acid oxidation genes CPT1α, . VTE also enhanced AMPK and blocked LXRα signaling in mouse livers. results indicated that VTE increased AMPK phosphorylation and reduced LXRα activity in HepG2 cells. Conversely, the antagonistic effect of VTE on LXRα was decreased through AMPK inhibition. Our data suggests that VTE may improve diet-induced NASH, which involves the pharmacological modulation of the AMPK-LXRα signaling pathway.
藤茶能改善糖脂代谢紊乱。然而,其在非酒精性脂肪性肝炎(NASH)中的保护作用及其潜在分子机制仍不清楚。抑制肝脏X受体α(LXRα)和激活腺苷单磷酸(AMP)激活的蛋白激酶(AMPK)可增强对NASH的控制。AMPK激活剂也已被证明可使LXRα失活。在此,使用蛋氨酸和胆碱缺乏的L-氨基酸饮食(MCDD)和高脂饮食(HFD)诱导的NASH小鼠,研究了剂量为1 g/100 g饮食的藤茶提取物(VTE)的抗NASH作用。使用TUNEL染色、AMPK抑制、蛋白质印迹、报告基因检测、qRT-PCR分析和免疫荧光探索了VTE的药理机制。VTE治疗改善了HFD诱导小鼠的脂肪肝,同时减轻了NASH的进展,包括预防MCDD喂养小鼠的肝脏脂质积累、脂肪变性、内质网应激、细胞凋亡、炎症和功能损伤。VTE降低了肝脏脂肪生成基因、F4/80、促炎细胞因子、CHOP和裂解的Caspase-3表达的作用,同时促进了脂肪酸氧化基因CPT1α的表达。VTE还增强了小鼠肝脏中的AMPK并阻断了LXRα信号传导。结果表明,VTE增加了HepG2细胞中AMPK的磷酸化并降低了LXRα的活性。相反,通过抑制AMPK,VTE对LXRα的拮抗作用降低。我们的数据表明,VTE可能改善饮食诱导的NASH,这涉及AMPK-LXRα信号通路的药理调节。