Effect of different bile acids on the intestine through enterohepatic circulation based on FXR

被引:84
作者
Xiang, Junwei [1 ,2 ]
Zhang, Zhengyan [1 ,2 ]
Xie, Hongyi [1 ,2 ]
Zhang, Chengcheng [1 ,2 ]
Bai, Yan [3 ]
Cao, Hua [4 ]
Che, Qishi [5 ]
Guo, Jiao [2 ]
Su, Zhengquan [1 ]
机构
[1] Guangdong Pharmaceut Univ, Guangdong Prov Univ Engn Technol, Res Ctr Nat Prod & Drugs, Guangdong Engn Res Ctr Nat Prod & New Drugs, Guangzhou, Peoples R China
[2] Guangdong Pharmaceut Univ, Guangdong Metab Dis Res Ctr Integrated Chinese &, Guangzhou, Peoples R China
[3] Guangdong Pharmaceut Univ, Sch Publ Hlth, Guangzhou, Peoples R China
[4] Guangdong Pharmaceut Univ, Sch Chem & Chem Engn, Guangdong Cosmet Engn & Technol Res Ctr, Zhongshan, Peoples R China
[5] Guangzhou Rainhome Pharm & Tech Co, Guangzhou, Peoples R China
关键词
Bile acids; enterohepatic circulation; intestine; FXR; FARNESOID-X-RECEPTOR; NEGATIVE FEEDBACK-REGULATION; NONALCOHOLIC STEATOHEPATITIS; ACTIVATED RECEPTORS; COLORECTAL-CANCER; OBETICHOLIC ACID; LIVER; GUT; MICROBIOTA; METABOLISM;
D O I
10.1080/19490976.2021.1949095
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Farnesoid X receptor (FXR) is a nuclear receptor for bile acids (BAs) that is widely expressed in the intestine, liver and kidney. FXR has important regulatory impacts on a wide variety of metabolic pathways (such as glucose, lipid, and sterol metabolism) and has been recognized to ameliorate obesity, liver damage, cholestasis and chronic inflammatory diseases. The types of BAs are complex and diverse. BAs link the intestine with the liver through the enterohepatic circulation. BAs derivatives have entered clinical trials for liver disease. In addition to the liver, the intestine is also targeted by BAs. This article reviews the effects of different BAs on the intestinal tract through the enterohepatic circulation from the perspective of FXR, aiming to elucidate the effects of different BAs on the intestinal tract and lay a foundation for new treatment methods.
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页数:17
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共 132 条
[1]   Farnesoid X receptor as marker of osteotropism of breast cancers through its role in the osteomimetism of tumor cells [J].
Absil, L. ;
Journe, F. ;
Larsimont, D. ;
Body, J. J. ;
Tafforeau, L. ;
Nonclercq, D. .
BMC CANCER, 2020, 20 (01)
[2]   Bile acids in glucose metabolism and insulin signalling - mechanisms and research needs [J].
Ahmad, Tiara R. ;
Haeusler, Rebecca A. .
NATURE REVIEWS ENDOCRINOLOGY, 2019, 15 (12) :701-712
[3]   Secondary bile acids: an underrecognized cause of colon cancer [J].
Ajouz, Hana ;
Mukherji, Deborah ;
Shamseddine, Ali .
WORLD JOURNAL OF SURGICAL ONCOLOGY, 2014, 12
[4]   The Receptor TGR5 Mediates the Prokinetic Actions of Intestinal Bile Acids and Is Required for Normal Defecation in Mice [J].
Alemi, Farzad ;
Poole, Daniel P. ;
Chiu, Jonathan ;
Schoonjans, Kristina ;
Cattaruzza, Fiore ;
Grider, John R. ;
Bunnett, Nigel W. ;
Corvera, Carlos U. .
GASTROENTEROLOGY, 2013, 144 (01) :145-154
[5]   Bile acids: regulation of apoptosis by ursodeoxycholic acid [J].
Amaral, Joana D. ;
Viana, Ricardo J. S. ;
Ramalho, Rita M. ;
Steer, Clifford J. ;
Rodrigues, Cecilia M. P. .
JOURNAL OF LIPID RESEARCH, 2009, 50 (09) :1721-1734
[6]   Gut microbiota in non-alcoholic fatty liver disease and alcohol-related liver disease: Current concepts and perspectives [J].
Arab, Juan P. ;
Arrese, Marco ;
Shah, Vijay H. .
HEPATOLOGY RESEARCH, 2020, 50 (04) :407-418
[7]   Bile Acids and Nonalcoholic Fatty Liver Disease: Molecular Insights and Therapeutic Perspectives [J].
Arab, Juan P. ;
Karpen, Saul J. ;
Dawson, Paul A. ;
Arrese, Marco ;
Trauner, Michael .
HEPATOLOGY, 2017, 65 (01) :350-362
[8]   Gut microbiota and human NAFLD: disentangling microbial signatures from metabolic disorders [J].
Aron-Wisnewsky, Judith ;
Vigliotti, Chloe ;
Witjes, Julia ;
Le, Phuong ;
Holleboom, Adriaan G. ;
Verheij, Joanne ;
Nieuwdorp, Max ;
Clement, Karine .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2020, 17 (05) :279-297
[9]   Carcinogenicity of deoxycholate, a secondary bile acid [J].
Bernstein, Carol ;
Holubec, Hana ;
Bhattacharyya, Achyut K. ;
Huy Nguyen ;
Payne, Claire M. ;
Zaitlin, Beryl ;
Bernstein, Harris .
ARCHIVES OF TOXICOLOGY, 2011, 85 (08) :863-871
[10]   Bile acids as endogenous etiologic agents in gastrointestinal cancer [J].
Bernstein, Harris ;
Bernstein, Carol ;
Payne, Claire M. ;
Dvorak, Katerina .
WORLD JOURNAL OF GASTROENTEROLOGY, 2009, 15 (27) :3329-3340