Gender Differences in Bile Acids and Microbiota in Relationship with Gender Dissimilarity in Steatosis Induced by Diet and FXR Inactivation

被引:100
作者
Sheng, Lili [1 ]
Jena, Prasant Kumar [1 ]
Liu, Hui-Xin [1 ]
Kalanetra, Karen M. [2 ]
Gonzalez, Frank J. [3 ]
French, Samuel W. [4 ]
Krishnan, Viswanathan V. [1 ,5 ]
Mills, David A. [2 ]
Wan, Yu-Jui Yvonne [1 ]
机构
[1] Univ Calif Davis, Dept Med Pathol & Lab Med, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Viticulture & Enol, Dept Food Sci & Technol, Davis, CA 95616 USA
[3] NCI, Lab Metab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[4] Harbor UCLA Med Ctr, Dept Pathol, Torrance, CA 90509 USA
[5] Fresno State Univ, Coll Sci & Math, Dept Chem, Fresno, CA USA
基金
美国国家卫生研究院;
关键词
FATTY LIVER-DISEASE; RETINOIC ACID; GUT MICROBIOME; INSULIN-RESISTANCE; DOWN-REGULATION; RECEPTOR; OBESITY; MICE; EXPRESSION; ACTIVATION;
D O I
10.1038/s41598-017-01576-9
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
This study aims to uncover how specific bacteria and bile acids (BAs) contribute to steatosis induced by diet and farnesoid X receptor (FXR) deficiency in both genders. A control diet (CD) and Western diet (WD), which contains high fat and carbohydrate, were used to feed wild type (WT) and FXR knockout (KO) mice followed by phenotyping characterization as well as BA and microbiota profiling. Our data revealed that male WD-fed FXR KO mice had the most severe steatosis and highest hepatic and serum lipids as well as insulin resistance among the eight studied groups. Gender differences in WDinduced steatosis, insulin sensitivity, and predicted microbiota functions were all FXR-dependent. FXR deficiency enriched Desulfovibrionaceae, Deferribacteraceae, and Helicobacteraceae, which were accompanied by increased hepatic taurine-conjugated cholic acid and beta-muricholic acid as well as hepatic and serum lipids. Additionally, distinct microbiota profiles were found in WD-fed WT mice harboring simple steatosis and CD-fed FXR KO mice, in which the steatosis had a potential to develop into liver cancer. Together, the presented data revealed FXR-dependent concomitant relationships between gut microbiota, BAs, and metabolic diseases in both genders. Gender differences in BAs and microbiota may account for gender dissimilarity in metabolism and metabolic diseases.
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页数:12
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