Suppr超能文献

2-十二烷基-6-甲氧基环己-2,5-二烯-1,4-二酮可减轻肝纤维化并改善肠道菌群和胆汁酸代谢。

2-Dodecyl-6-methoxycyclohexa-2,5-dien-1,4-dione alleviates liver fibrosis and improves intestinal flora and bile acid metabolism.

作者信息

He Yongfei, Hoa Pham Thi Thai, Xu Junming, Hong Shengjie, Wang Jicai, Zhai Hang, Tao Qiang, Li Ruixi, Zhang Guangquan, Shi Xianjie

机构信息

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.

出版信息

Front Pharmacol. 2025 May 16;16:1581138. doi: 10.3389/fphar.2025.1581138. eCollection 2025.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

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。

方法

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

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3073/12122303/ee454cc5cf6f/fphar-16-1581138-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验