The Relationship between the Gut Microbiome and Metformin as a Key for Treating Type 2 Diabetes Mellitus

被引:83
|
作者
Lee, Chae Bin [1 ,2 ]
Chae, Soon Uk [1 ,2 ]
Jo, Seong Jun [1 ,2 ]
Jerng, Ui Min [3 ]
Bae, Soo Kyung [1 ,2 ]
机构
[1] Catholic Univ Korea, Coll Pharm, Bucheon 14662, South Korea
[2] Catholic Univ Korea, Integrated Res Inst Pharmaceut Sci, Bucheon 14662, South Korea
[3] Sangji Univ, Coll Korean Med, Dept Internal Med, Wonju 26339, South Korea
基金
新加坡国家研究基金会;
关键词
gut microbiome; type 2 diabetes mellitus; metformin; dysbiosis;
D O I
10.3390/ijms22073566
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metformin is the first-line pharmacotherapy for treating type 2 diabetes mellitus (T2DM); however, its mechanism of modulating glucose metabolism is elusive. Recent advances have identified the gut as a potential target of metformin. As patients with metabolic disorders exhibit dysbiosis, the gut microbiome has garnered interest as a potential target for metabolic disease. Henceforth, studies have focused on unraveling the relationship of metabolic disorders with the human gut microbiome. According to various metagenome studies, gut dysbiosis is evident in T2DM patients. Besides this, alterations in the gut microbiome were also observed in the metformin-treated T2DM patients compared to the non-treated T2DM patients. Thus, several studies on rodents have suggested potential mechanisms interacting with the gut microbiome, including regulation of glucose metabolism, an increase in short-chain fatty acids, strengthening intestinal permeability against lipopolysaccharides, modulating the immune response, and interaction with bile acids. Furthermore, human studies have demonstrated evidence substantiating the hypotheses based on rodent studies. This review discusses the current knowledge of how metformin modulates T2DM with respect to the gut microbiome and discusses the prospect of harnessing this mechanism in treating T2DM.
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页数:26
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