High-Fat Diet-Induced Decreased Circulating Bile Acids Contribute to Obesity Associated with Gut Microbiota in Mice

被引:26
作者
Cai, Haiying [1 ,2 ,3 ]
Zhang, Junhui [2 ]
Liu, Chang [1 ]
Le, Thanh Ninh [3 ]
Lu, Yuyun [3 ]
Feng, Fengqin [2 ]
Zhao, Minjie [2 ]
机构
[1] Zhejiang Univ Sci & Technol, Sch Biol & Chem Engn, Hangzhou 310023, Peoples R China
[2] Zhejiang Univ, Coll Biosyst Engn & Food Sci, Hangzhou 310058, Peoples R China
[3] Natl Univ Singapore, Dept Food Sci & Technol, Singapore 117542, Singapore
基金
中国国家自然科学基金;
关键词
obesity; bile acids; lipid homeostasis; gut microbiota; high-fat diet; FARNESOID-X-RECEPTOR; HOMEOSTASIS; TRANSPORTER; ACTIVATION; BETA;
D O I
10.3390/foods13050699
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The altered circulating bile acids (BAs) modulate gut microbiota, energy metabolism and various physiological functions. BA profiles in liver, serum, ileum and feces of HFD-fed mice were analyzed with normal chow diet (NCD)-fed mice after 16-week feeding. Furthermore, gut microbiota was analyzed and its correlation analysis with BA was performed. The result showed that long-term HFD feeding significantly decreased hepatic and serum BA levels, mainly attributed to the inhibition of hepatic BA synthesis and the reduced reabsorption efficiency of BAs in enterohepatic circulation. It also significantly impaired glucose and lipid homeostasis and gut microbiota in mice. We found significantly higher bile salt hydrolase activity in ileal microbes and a higher ratio of free BAs to conjugated BA content in ileal contents in HFD groups compared with NCD group mice, which might account for the activated intestinal farnesoid X receptor signaling on liver BA synthesis inhibition and reduced ileal reabsorption. The decreased circulating BAs were associated with the dysregulation of the lipid metabolism according to the decreased TGR5 signaling in the ileum and BAT. In addition, it is astonishing to find extremely high percentages of taurocholate and 12-OH BAs in liver and serum BA profiles of both groups, which was mainly attributed to the high substrate selectivity for 12-OH BAs of the intestinal BAs transporter during the ileal reabsorption of enterohepatic circulation. This study revealed a significant effect of long-term HFD feeding on the decreased circulating BA pool in mice, which impaired lipid homeostasis and gut microbiota, and collectively resulted in metabolic disorders and obesity.
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页数:19
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共 44 条
[1]   OST alpha-OST beta: a key membrane transporter of bile acids and conjugated steroids [J].
Ballatori, Nazzareno ;
Li, Na ;
Fang, Fang ;
Boyer, James L. ;
Christian, Whitney V. ;
Hammond, Christine L. .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2009, 14 :2829-2844
[2]   Regulation of hepatic metabolic pathways by the orphan nuclear receptor SHP [J].
Boulias, K ;
Katrakili, N ;
Bamberg, K ;
Underhill, P ;
Greenfield, A ;
Talianidis, I .
EMBO JOURNAL, 2005, 24 (14) :2624-2633
[3]   Intestinal Farnesoid X Receptor and Takeda G Protein Couple Receptor 5 Signaling in Metabolic Regulation [J].
Chiang, John Y. L. ;
Pathak, Preeti ;
Liu, Hailiang ;
Donepudi, Ajay ;
Ferrell, Jessica ;
Boehme, Shannon .
DIGESTIVE DISEASES, 2017, 35 (03) :241-245
[4]   FXR activation protects against NAFLD via bile-acid-dependent reductions in lipid absorption [J].
Clifford, Bethan L. ;
Sedgeman, Leslie R. ;
Williams, Kevin J. ;
Morand, Pauline ;
Cheng, Angela ;
Jarrett, Kelsey E. ;
Chan, Alvin P. ;
Brearley-Sholto, Madelaine C. ;
Wahlstrom, Annika ;
Ashby, Julianne W. ;
Barshop, William ;
Wohlschlegel, James ;
Calkin, Anna C. ;
Liu, Yingying ;
Thorell, Anders ;
Meikle, Peter J. ;
Drew, Brian G. ;
Mack, Julia J. ;
Marschall, Hanns-Ulrich ;
Tarling, Elizabeth J. ;
Edwards, Peter A. ;
Vallim, Thomas Q. de Aguiar .
CELL METABOLISM, 2021, 33 (08) :1671-+
[5]   Expression and transport properties of the human ileal and renal sodium-dependent bile acid transporter [J].
Craddock, AL ;
Love, MW ;
Daniel, RW ;
Kirby, LC ;
Walters, HC ;
Wong, MH ;
Dawson, PA .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1998, 274 (01) :G157-G169
[6]   Beneficial Effect of Caffeic Acid Phenethyl Ester (CAPE) on Hepatocyte Damage Induced by Bile Duct Ligation: An Electron Microscopic Examination [J].
Esrefoglu, Mukaddes ;
Ara, Cengiz .
ULTRASTRUCTURAL PATHOLOGY, 2010, 34 (05) :273-278
[7]   Gut microbiota in human metabolic health and disease [J].
Fan, Yong ;
Pedersen, Oluf .
NATURE REVIEWS MICROBIOLOGY, 2021, 19 (01) :55-71
[8]   Intestinal Farnesoid X Receptor Signaling Modulates Metabolic Disease [J].
Gonzalez, Frank J. ;
Jiang, Changtao ;
Xie, Cen ;
Patterson, Andrew D. .
DIGESTIVE DISEASES, 2017, 35 (03) :178-184
[9]   An Intestinal Microbiota-Farnesoid X Receptor Axis Modulates Metabolic Disease [J].
Gonzalez, Frank J. ;
Jiang, Changtao ;
Patterson, Andrew D. .
GASTROENTEROLOGY, 2016, 151 (05) :845-859
[10]   Human Insulin Resistance Is Associated With Increased Plasma Levels of 12a-Hydroxylated Bile Acids [J].
Haeusler, Rebecca A. ;
Astiarraga, Brenno ;
Camastra, Stefania ;
Accili, Domenico ;
Ferrannini, Ele .
DIABETES, 2013, 62 (12) :4184-4191