He Yongfei, Hoa Pham Thi Thai, Xu Junming, Hong Shengjie, Wang Jicai, Zhai Hang, Tao Qiang, Li Ruixi, Zhang Guangquan, Shi Xianjie
Department of Hepatobiliary and Pancreatic Surgery, The Eighth Affiliated Hospital of Sun Yat-sen University, Shenzhen, Guangdong, China.
Zhuang & Yao Medicine Research and Development Center, Guangxi International Zhuang Medicine Hospital is Affiliated to Guangxi University of Chinese Medicine, Nanning, Guangxi Zhuang, China.
Front Pharmacol. 2025 May 16;16:1581138. doi: 10.3389/fphar.2025.1581138. eCollection 2025.
The bioactive compound 2-Dodecyl-6-methoxycyclohexa-2,5-diene-1,4-dione (DMDD), derived from the horn root of star fruit, exhibits therapeutic promise through its modulation of the TGF-β1 pathway and regulation of bile acids.
In this study, a liver fibrosis model was established in Kunming mice (KM) induced by carbon tetrachloride (CCL4), and DMDD (50 mg/kg) was administered intragastrically. HE staining, Masson staining, and Sirius staining were used to evaluate the effect of DMDD on liver fibrosis. The Illumina sequencing platform was used to detect intestinal flora and liver transcriptome information in mouse feces, and high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) technology was used to detect bile acid content changes in mouse feces.
The results show that DMDD can mitigate liver fibrosis-induced damage in mice, potentially through the suppression of the TGF-β/Smad signaling pathway. Furthermore, DMDD increased the abundance of , , , , and , thereby addressing intestinal flora disturbances and regulating bile acid metabolism.
Our study suggests that DMDD alleviates liver fibrosis by inhibiting the TGF-β/Smad signaling pathway, restoring gut microbiota homeostasis, and balancing bile acid metabolism.
从杨桃果柄中提取的生物活性化合物2-十二烷基-6-甲氧基环己-2,5-二烯-1,4-二酮(DMDD),通过调节TGF-β1信号通路和胆汁酸代谢展现出治疗潜力。
本研究通过四氯化碳(CCl4)诱导建立昆明小鼠(KM)肝纤维化模型,并对其进行DMDD(50mg/kg)灌胃处理。采用苏木精-伊红(HE)染色、Masson染色和天狼星染色评估DMDD对肝纤维化的影响。利用Illumina测序平台检测小鼠粪便中的肠道菌群和肝脏转录组信息,采用高效液相色谱-串联质谱(HPLC-MS/MS)技术检测小鼠粪便中胆汁酸含量变化。
结果表明,DMDD可能通过抑制TGF-β/Smad信号通路减轻小鼠肝纤维化损伤。此外,DMDD增加了[此处原文缺失具体菌属名称]、[此处原文缺失具体菌属名称]、[此处原文缺失具体菌属名称]、[此处原文缺失具体菌属名称]和[此处原文缺失具体菌属名称]的丰度,从而改善肠道菌群紊乱并调节胆汁酸代谢。
我们的研究表明,DMDD通过抑制TGF-β/Smad信号通路、恢复肠道微生物群稳态和平衡胆汁酸代谢来减轻肝纤维化。