Novel approaches in IBD therapy: targeting the gut microbiota-bile acid axis

被引:10
|
作者
Pan, Yinping [1 ]
Zhang, Haojie [1 ]
Li, Minghui [1 ]
He, Tingjing [1 ]
Guo, Sihao [1 ]
Zhu, Liancai [1 ,3 ]
Tan, Jun [2 ]
Wang, Bochu [1 ,3 ]
机构
[1] Chongqing Univ, Coll Bioengn, Key Lab Biorheol Sci & Technol, Minist Educ, Chongqing, Peoples R China
[2] Chongqing Univ Educ, Sch Biol & Chem Engn, Chongqing Key Lab Med Resources Three Gorges Reser, Chongqing, Peoples R China
[3] Chongqing Univ, Bioengn Coll, 174 Shapingba Main St, Chongqing 400030, Peoples R China
关键词
Inflammatory bowel disease; gut microbiota; bile acid biotransformation; bile acid-activated receptor; engineered bacteria; INFLAMMATORY-BOWEL-DISEASE; 3-ALPHA-HYDROXYSTEROID DEHYDROGENASE TYPE-3; STEROID 5-BETA-REDUCTASE AKR1D1; STRAIN VPI 12708; NF-KAPPA-B; SALT HYDROLASE; ULCERATIVE-COLITIS; LITHOCHOLIC ACID; DEOXYCHOLIC-ACID; 7-ALPHA-HYDROXYSTEROID DEHYDROGENASE;
D O I
10.1080/19490976.2024.2356284
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Inflammatory bowel disease (IBD) is a chronic and recurrent condition affecting the gastrointestinal tract. Disturbed gut microbiota and abnormal bile acid (BA) metabolism are notable in IBD, suggesting a bidirectional relationship. Specifically, the diversity of the gut microbiota influences BA composition, whereas altered BA profiles can disrupt the microbiota. IBD patients often exhibit increased primary bile acid and reduced secondary bile acid concentrations due to a diminished bacteria population essential for BA metabolism. This imbalance activates BA receptors, undermining intestinal integrity and immune function. Consequently, targeting the microbiota-BA axis may rectify these disturbances, offering symptomatic relief in IBD. Here, the interplay between gut microbiota and bile acids (BAs) is reviewed, with a particular focus on the role of gut microbiota in mediating bile acid biotransformation, and contributions of the gut microbiota-BA axis to IBD pathology to unveil potential novel therapeutic avenues for IBD.
引用
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页数:33
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