TY - JOUR
T1 - Oral treatment with improves insulin sensitivity in mice
AU - Udayappan, Shanthadevi
AU - Manneras-Holm, Louise
AU - Chaplin-Scott, Alice
AU - Belzer, Clara
AU - Herrema, Hilde
AU - Dallinga-Thie, Geesje M
AU - Duncan, Silvia H
AU - Stroes, Erik S G
AU - Groen, Albert K
AU - Flint, Harry J
AU - Backhed, Fredrik
AU - de Vos, Willem M
AU - Nieuwdorp, Max
PY - 2016
Y1 - 2016
N2 - An altered intestinal microbiota composition is associated with insulin resistance and type 2 diabetes mellitus. We previously identified increased intestinal levels of Eubacterium hallii, an anaerobic bacterium belonging to the butyrate-producing Lachnospiraceae family, in metabolic syndrome subjects who received a faecal transplant from a lean donor. To further assess the effects of E. hallii on insulin sensitivity, we orally treated obese and diabetic db/db mice with alive E. hallii and glycerol or heat-inactive E. hallii as control. Insulin tolerance tests and hyperinsulinemic-euglycemic clamp experiments revealed that alive E. hallii treatment improved insulin sensitivity compared control treatment. In addition, E. hallii treatment increased energy expenditure in db/db mice. Active E. hallii treatment was found to increase faecal butyrate concentrations and to modify bile acid metabolism compared with heat-inactivated controls. Our data suggest that E. hallii administration potentially alters the function of the intestinal microbiome and that microbial metabolites may contribute to the improved metabolic phenotype.
AB - An altered intestinal microbiota composition is associated with insulin resistance and type 2 diabetes mellitus. We previously identified increased intestinal levels of Eubacterium hallii, an anaerobic bacterium belonging to the butyrate-producing Lachnospiraceae family, in metabolic syndrome subjects who received a faecal transplant from a lean donor. To further assess the effects of E. hallii on insulin sensitivity, we orally treated obese and diabetic db/db mice with alive E. hallii and glycerol or heat-inactive E. hallii as control. Insulin tolerance tests and hyperinsulinemic-euglycemic clamp experiments revealed that alive E. hallii treatment improved insulin sensitivity compared control treatment. In addition, E. hallii treatment increased energy expenditure in db/db mice. Active E. hallii treatment was found to increase faecal butyrate concentrations and to modify bile acid metabolism compared with heat-inactivated controls. Our data suggest that E. hallii administration potentially alters the function of the intestinal microbiome and that microbial metabolites may contribute to the improved metabolic phenotype.
U2 - 10.1038/npjbiofilms.2016.9
DO - 10.1038/npjbiofilms.2016.9
M3 - Journal article
C2 - 28721246
SN - 2055-5008
VL - 2
JO - npj Biofilms and Microbiomes
JF - npj Biofilms and Microbiomes
M1 - 16009
ER -