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Alteration of gut microbiota by vancomycin and bacitracin improves insulin resistance via glucagon-like peptide 1 in diet-induced obesity.

作者信息

Hwang Injae, Park Yoon Jeong, Kim Yeon-Ran, Kim Yo Na, Ka Sojeong, Lee Ho Young, Seong Je Kyung, Seok Yeong-Jae, Kim Jae Bum

机构信息

*Department of Biological Sciences, Institute of Molecular Biology and Genetics, Department of Biophysics and Chemical Biology, College of Veterinary Medicine, and College of Medicine, Seoul National University, Seoul, Korea.

*Department of Biological Sciences, Institute of Molecular Biology and Genetics, Department of Biophysics and Chemical Biology, College of Veterinary Medicine, and College of Medicine, Seoul National University, Seoul, Korea

出版信息

FASEB J. 2015 Jun;29(6):2397-411. doi: 10.1096/fj.14-265983. Epub 2015 Feb 20.


DOI:10.1096/fj.14-265983
PMID:25713030
Abstract

Firmicutes and Bacteroidetes, 2 major phyla of gut microbiota, are involved in lipid and bile acid metabolism to maintain systemic energy homeostasis in host. Recently, accumulating evidence has suggested that dietary changes promptly induce the alteration of abundance of both Firmicutes and Bacteroidetes in obesity and its related metabolic diseases. Nevertheless, the metabolic roles of Firmicutes and Bacteroidetes on such disease states remain unclear. The aim of this study was to determine the effects of antibiotic-induced depletion of Firmicutes and Bacteroidetes on dysregulation of energy homeostasis in obesity. Treatment of C57BL/6J mice with the antibiotics (vancomycin [V] and bacitracin [B]), in the drinking water, before diet-induced obesity (DIO) greatly decreased both Firmicutes and Bacteroidetes in the gut as revealed by pyrosequencing of the microbial 16S rRNA gene. Concomitantly, systemic glucose intolerance, hyperinsulinemia, and insulin resistance in DIO were ameliorated via augmentation of GLP-1 secretion (active form; 2.03-fold, total form; 5.09-fold) independently of obesity as compared with untreated DIO controls. Furthermore, there were increases in metabolically beneficial metabolites derived from the gut. Together, our data suggest that Firmicutes and Bacteroidetes potentially mediate insulin resistance through modulation of GLP-1 secretion in obesity.

摘要

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