Affiliation:
1. Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, USA
Abstract
The gut microbial community has a profound influence on host physiology in both health and disease. In diabetic individuals, the gut microbiota can affect the course of disease, and some medications for diabetes, including metformin, seem to elicit some of their benefits via an interaction with the microbiota. Here, we report that acarbose, a glucoamylase inhibitor for type 2 diabetes, changes the murine gut bacterial community structure in a reversible and diet-dependent manner. In both high-starch and high-fiber diet backgrounds, acarbose treatment results in increased short-chain fatty acids, particularly butyrate, as measured in stool samples. As we learn more about how human disease is affected by the intestinal bacterial community, the interplay between medications such as acarbose and the diet will become increasingly important to evaluate.
Funder
Human Microbiome Initiative, University of Michigan
HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
78 articles.
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