Ginsenoside Rh4 inhibits colorectal cancer via the modulation of gut microbiota-mediated bile acid metabolism

被引:6
作者
Bai, Xue [1 ,2 ]
Duan, Zhiguang [1 ,2 ]
Deng, Jianjun [1 ,2 ]
Zhang, Zhuo [3 ]
Fu, Rongzhan [1 ,2 ]
Zhu, Chenhui [1 ,2 ]
Fan, Daidi [1 ,2 ]
机构
[1] Northwest Univ, Engn Res Ctr Western Resource Innovat Med Green Mf, Sch Chem Engn, Minist Educ, Xian 710069, Peoples R China
[2] Northwest Univ, Biotech & Biomed Res Inst, Xian 710069, Peoples R China
[3] Xi An Jiao Tong Univ, Affiliated Hosp 1, Plast & Cosmet Maxillofacial Surg, Xian 710061, Peoples R China
基金
中国国家自然科学基金;
关键词
Gut microbiota; Bile acid; Ursodeoxycholic acid; Akkermansia muciniphila; Colorectal cancer; Ginsenoside; URSODEOXYCHOLIC ACID; NUCLEAR RECEPTOR; PANAX-GINSENG; PROTECTS; CELLS; FXR;
D O I
10.1016/j.jare.2024.06.028
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: Dysbiosis of the gut microbiota is emerging as a pivotal factor in the pathogenesis of colorectal cancer (CRC). Ginsenoside Rh4 (Rh4) is an active compound isolated from ginseng with beneficial effects in modulating intestinal inflammation and gut microbiota dysbiosis, but how Rh4 regulates the gut microbiota to alleviate CRC remains underexplored. Objectives: We investigated the impact of Rh4 on CRC and the mechanism of its action in inhibiting CRC via modulation of gut microbiota. Methods: We used the AOM/DSS model and employed transcriptomics, genomics and metabolomics techniques to explore the inhibitory impact of Rh4 on CRC. Furthermore, we employed experiments involving antibiotic treatment and fecal microbiota transplantation (FMT) to investigate the role of the gut microbiota. Finally, we elucidated the pivotal role of key functional bacteria and metabolites regulated by Rh4 in CRC. Results: Our research findings indicated that Rh4 repaired intestinal barrier damage caused by CRC, alleviated intestinal inflammation, and inhibited the development of CRC. Additionally, Rh4 inhibited CRC in a gut microbiota-dependent manner. Rh4 increased the diversity of gut microbiota, enriched the probiotic Akkermansia muciniphila (A. muciniphila), and alleviated gut microbiota dysbiosis caused by CRC. Subsequently, Rh4 regulated A. muciniphila-mediated bile acid metabolism. A. muciniphila promoted the production of UDCA by enhancing the activity of 7a-hydroxysteroid dehydrogenase (7a-HSDH).UDCA further activated FXR, modulated the TLR4-NF-jB signaling pathway, thus inhibiting the develop-ment of CRC. Conclusion: Our results confirm that Rh4 inhibits CRC in a gut microbiota-dependent manner by modu-lating gut microbiota-mediated bile acid metabolism and promoting the production of UDCA, which fur-ther activates the FXR receptor and regulates the TLR4-NF-jB signaling pathway. Our results confirm that Rh4 has the potential to be used as a modulator of gut microbiota for preventing and treatment of CRC. (c) 2024 The Authors. Published by Elsevier B.V. on behalf of Cairo University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:37 / 52
页数:16
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