The role of gut microbiota in the resistance to obesity in mice fed a high fat diet

被引:65
作者
Cao, Wanxiu [1 ]
Chin, Yaoxian [1 ]
Chen, Xin [1 ]
Mi, Ye [1 ]
Xue, Changhu [1 ,2 ]
Wang, Yuming [1 ]
Tang, Qingjuan [1 ]
机构
[1] Ocean Univ China, Coll Food Sci & Engn, Qingdao, Shandong, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, Qingdao, Shandong, Peoples R China
基金
国家重点研发计划;
关键词
Gut microbiota; high fat diet; obesity; resistance; INSULIN-RESISTANCE; INFLAMMATION; METABOLISM; DISORDERS; PROTECTS; MOUSE;
D O I
10.1080/09637486.2019.1686608
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The prevalence of diet induced obesity (DIO) is a huge threat to global health. Differences in gut microbiota may be concerned with DIO. Sixty male C57BL/6J mice were fed with high fat diet (HFD, 45% kcal from fat) for 16 weeks. Among them, body weight, body fat rate and the lipid content in plasma or liver of six mice (Lean (L) group) were obviously lower than average levels (Fatty (F) group). These results supported that some individuals were resistant to HFD induced obesity. Using 16S rRNA analysis to investigate the role of gut microbiota in this resistance, we found several alterations associated with the resistance, such as an increase of Muribaculaceae in L group. Moreover, analysis of predicted microbial function suggested that bacteria in F group could better utilise HFD compared to L group. In conclusion, gut microbiota might play a bigger role than diet in resisting obesity, and it could be a potential target for obesity treatment.
引用
收藏
页码:453 / 463
页数:11
相关论文
共 46 条
[41]   Distinct signatures of host-microbial meta-metabolome and gut microbiome in two C57BL/6 strains under high-fat diet [J].
Walker, Alesia ;
Pfitzner, Barbara ;
Neschen, Susanne ;
Kahle, Melanie ;
Harir, Mourad ;
Lucio, Marianna ;
Moritz, Franco ;
Tziotis, Dimitrios ;
Witting, Michael ;
Rothballer, Michael ;
Engel, Marion ;
Schmid, Michael ;
Endesfelder, David ;
Klingenspor, Martin ;
Rattei, Thomas ;
Castell, Wolfgang zu ;
de Angelis, Martin Hrabe ;
Hartmann, Anton ;
Schmitt-Kopplin, Philippe .
ISME JOURNAL, 2014, 8 (12) :2380-2396
[42]   Meta-analyses of human gut microbes associated with obesity and IBD [J].
Walters, William A. ;
Xu, Zech ;
Knight, Rob .
FEBS LETTERS, 2014, 588 (22) :4223-4233
[43]  
Xin XG, 2000, BRAIN RES BULL, V52, P235, DOI 10.1016/S0361-9230(00)00228-8
[44]   Effect of piceatannol on circadian Per2 expression in vitro and in vivo [J].
Yamamoto, Takayuki ;
Iwami, Shiho ;
Aoyama, Shinya ;
Maruki-Uchida, Hiroko ;
Mori, Sadao ;
Hirooka, Rina ;
Takahashi, Kengo ;
Morita, Minoru ;
Shibata, Shigenobu .
JOURNAL OF FUNCTIONAL FOODS, 2019, 56 :49-56
[45]   Colonic inflammation accompanies an increase of β-catenin signaling and Lachnospiraceae/Streptococcaceae bacteria in the hind gut of high-fat diet-fed mice [J].
Zeng, Huawei ;
Ishaq, Suzanne L. ;
Zhao, Feng-Qi ;
Wright, Andre-Denis G. .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2016, 35 :30-36
[46]   Neoagarotetraose protects mice against intense exercise-induced fatigue damage by modulating gut microbial composition and function [J].
Zhang, Na ;
Mao, Xiangzhao ;
Li, Robert W. ;
Hou, Enling ;
Wang, Yuming ;
Xue, Changhu ;
Tang, Qingjuan .
MOLECULAR NUTRITION & FOOD RESEARCH, 2017, 61 (08)