Key Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Laboratory of Ethnomedicine of Ministry of Education, Zunyi Medical University, Zunyi 563000, China.
Department of Pharmacology, Key Laboratory of Basic Pharmacology of Guizhou Province and School of Pharmacy, Zunyi Medical University, Zunyi 563000, China.
J Agric Food Chem. 2024 Oct 30;72(43):23819-23831. doi: 10.1021/acs.jafc.4c04131. Epub 2024 Aug 21.
Trilobatin, a novel natural food additive, exerts a protective effect on acute liver injury. However, whether Trilobatin can protect against alcoholic liver disease (ALD) has not been elucidated. This research is intended to ascertain the impact of Trilobatin on ALD in mice and decipher the potential underlying mechanisms. Lieber-DeCarli liquid alcohol diet was used to induce ALD in mice, followed by administration of Trilobatin (10, 20, 40 mg·kg·d) for 15 days. The results suggested that Trilobatin significantly alleviated ethanol-induced hepatic injury in mice. Furthermore, RNA-Seq analysis revealed that yes-associated protein (YAP) downregulation occurred in the liver after Trilobatin treatment. Mechanistically, Trilobatin directly bound to YAP and hindered its nuclear translocation, which activated the Nrf2 pathway to reduce pro-inflammatory cytokines and oxidative stress. Intriguingly, 16S rDNA analysis results revealed that Trilobatin reshaped the gut microbiota, reducing harmful bacteria and increasing beneficial bacteria. It also enhanced tight junction proteins, defending against damage to the intestinal barrier. These findings not only highlight the microbiota-gut-liver axis and YAP/Nrf2 pathway as crucial potential targets to treat ALD but also reveal that Trilobatin effectively protects against ALD, at least partly, through modulating the microbiota-gut-liver axis and YAP/Nrf2 pathway.
三叶香茶菜甲素是一种新型天然食品添加剂,对急性肝损伤具有保护作用。然而,三叶香茶菜甲素是否对酒精性肝病(ALD)具有保护作用尚未阐明。本研究旨在确定三叶香茶菜甲素对小鼠 ALD 的影响,并探讨其潜在的作用机制。采用 Lieber-DeCarli 液体酒精饮食诱导小鼠 ALD,然后给予三叶香茶菜甲素(10、20、40mg·kg·d)治疗 15 天。结果表明,三叶香茶菜甲素可显著减轻乙醇诱导的小鼠肝损伤。此外,RNA-Seq 分析显示,三叶香茶菜甲素处理后肝脏中 YAP(yes-associated protein)下调。机制上,三叶香茶菜甲素直接与 YAP 结合,阻止其核转位,激活 Nrf2 通路,减少促炎细胞因子和氧化应激。有趣的是,16S rDNA 分析结果显示,三叶香茶菜甲素重塑了肠道微生物群,减少了有害细菌,增加了有益细菌。它还增强了紧密连接蛋白,防止肠道屏障受损。这些发现不仅强调了微生物群-肠道-肝脏轴和 YAP/Nrf2 通路是治疗 ALD 的重要潜在靶点,还揭示了三叶香茶菜甲素通过调节微生物群-肠道-肝脏轴和 YAP/Nrf2 通路有效防治 ALD,至少部分是通过调节微生物群-肠道-肝脏轴和 YAP/Nrf2 通路。