The therapeutic potential of manipulating gut microbiota in obesity and type 2 diabetes mellitus

被引:271
|
作者
Kootte, R. S. [1 ]
Vrieze, A. [2 ]
Holleman, F. [2 ]
Dallinga-Thie, G. M. [1 ]
Zoetendal, E. G. [3 ]
de Vos, W. M. [3 ,4 ]
Groen, A. K. [5 ]
Hoekstra, J. B. L. [2 ]
Stroes, E. S. [1 ]
Nieuwdorp, M. [1 ,2 ]
机构
[1] Univ Amsterdam, Dept Vasc Med, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Dept Internal Med, NL-1105 AZ Amsterdam, Netherlands
[3] Wageningen Univ, Microbiol Lab, Wageningen, Netherlands
[4] Univ Helsinki, Dept Basic Vet Med, Helsinki, Finland
[5] Univ Groningen, Univ Med Ctr Groningen, Ctr Liver Digest & Metab Dis, Groningen, Netherlands
来源
DIABETES OBESITY & METABOLISM | 2012年 / 14卷 / 02期
关键词
antibiotics; bile acids; gut microbiota; microbial transplantation; obesity; prebiotics; probiotics; SCFA; type 2 diabetes mellitus; DIET-INDUCED OBESITY; GLUCAGON-LIKE PEPTIDE-1; LACTOBACILLUS-CASEI; IN-VIVO; METAGENOMIC ANALYSIS; BILE-ACIDS; INTESTINAL MICROBIOTA; BACTERIAL COMMUNITY; INSULIN-RESISTANCE; GLUCOSE-TOLERANCE;
D O I
10.1111/j.1463-1326.2011.01483.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Obesity and type 2 diabetes mellitus (T2DM) are attributed to a combination of genetic susceptibility and lifestyle factors. Their increasing prevalence necessitates further studies on modifiable causative factors and novel treatment options. The gut microbiota has emerged as an important contributor to the obesity-and T2DM-epidemic proposed to act by increasing energy harvest from the diet. Although obesity is associated with substantial changes in the composition and metabolic function of the gut microbiota, the pathophysiological processes remain only partly understood. In this review we will describe the development of the adult human microbiome and discuss how the composition of the gut microbiota changes in response to modulating factors. The influence of short-chain fatty acids, bile acids, prebiotics, probiotics, antibiotics and microbial transplantation is discussed from studies using animal and human models. Ultimately, we aim to translate these findings into therapeutic pathways for obesity and T2DM in humans.
引用
收藏
页码:112 / 120
页数:9
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