Microbial modulation of energy availability in the colon regulates intestinal transit

Wichmann, Anita;Allahyar, Ava;Greiner, Thomas U;Plovier, Hubert;Bäckhed, Fredrik;et.al.
(2013) Cell Host & Microbe — Vol. 14, n° 5, p. 582-590 (2013)

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Authors
  • Wichmann, Anita
    Author
  • Allahyar, Ava
    Author
  • Greiner, Thomas U
    Author
  • Plovier, Hubert
    Author
  • Author
  • Cani, Patriceorcid-logoUCLouvain
    Author
  • Bäckhed, Fredrik
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Abstract
Gut microbiota contribute to host metabolic efficiency by increasing energy availability through the fermentation of dietary fiber and production of short-chain fatty acids (SCFAs) in the colon. SCFAs are proposed to stimulate secretion of the proglucagon (Gcg)-derived incretin hormone GLP-1, which stimulates insulin secretion (incretin response) and inhibits gastric emptying. We find that germ-free (GF) and antibiotic-treated mice, which have severely reduced SCFA levels, have increased basal GLP-1 levels in the plasma and increased Gcg expression in the colon. Increasing energy supply, either through colonization with polysaccharide-fermenting bacteria or through diet, suppressed colonic Gcg expression in GF mice. Increased GLP-1 levels in GF mice did not improve the incretin response but instead slowed intestinal transit. Thus, microbiota regulate the basal levels of GLP-1, and increasing these levels may be an adaptive response to insufficient energy availability in the colon that slows intestinal transit and allows for greater nutrient absorption.
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Citations

Wichmann, A., Allahyar, A., Greiner, T. U., Plovier, H., Lundén, G. Ö., Larsson, T., Drucker, D. J., Delzenne, N., Cani, P., & Bäckhed, F. (2013). Microbial modulation of energy availability in the colon regulates intestinal transit. Cell Host & Microbe, 14(5), 582-590. https://doi.org/10.1016/j.chom.2013.09.012 (Original work published 2013)