Targeting the gastrointestinal tract to treat type 2 diabetes

被引:18
作者
Bauer, Paige V. [1 ,2 ,3 ]
Duca, Frank A. [1 ,2 ]
机构
[1] Toronto Gen Hosp, Res Inst, Toronto, ON, Canada
[2] UHN, Dept Med, Toronto, ON, Canada
[3] Univ Toronto, Dept Physiol, Toronto, ON, Canada
关键词
gut; metformin; gut sensing; gut microbiota; bile acids; GLUCAGON-LIKE PEPTIDE-1; Y GASTRIC BYPASS; DUODENAL-JEJUNAL BYPASS; FARNESOID-X-RECEPTOR; VERTICAL SLEEVE GASTRECTOMY; PROTEIN-COUPLED RECEPTOR; GROWTH-FACTOR; 19; OLIGOFRUCTOSE PROMOTES SATIETY; LOWERS GLUCOSE-PRODUCTION; HUMAN GUT MICROBIOTA;
D O I
10.1530/JOE-16-0056
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The rising global rates of type 2 diabetes and obesity present a significant economic and social burden, underscoring the importance for effective and safe therapeutic options. The success of glucagon-like-peptide-1 receptor agonists in the treatment of type 2 diabetes, along with the potent glucose-lowering effects of bariatric surgery, highlight the gastrointestinal tract as a potential target for diabetes treatment. Furthermore, recent evidence suggests that the gut plays a prominent role in the ability of metformin to lower glucose levels. As such, the current review highlights some of the current and potential pathways in the gut that could be targeted to improve glucose homeostasis, such as changes in nutrient sensing, gut peptides, gut microbiota and bile acids. A better understanding of these pathways will lay the groundwork for novel gut-targeted antidiabetic therapies, some of which have already shown initial promise.
引用
收藏
页码:R95 / R113
页数:19
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