Early life antibiotic exposure affects pancreatic islet development and metabolic regulation

被引:28
作者
Li, Jiaying [1 ]
Yang, Kaiyuan [1 ]
Ju, Tingting [1 ]
Ho, Tracy [1 ]
McKay, Catharine A. [1 ]
Gao, Yanhua [1 ]
Forget, Shay K. [1 ]
Gartner, Stephanie R. [1 ]
Field, Catherine J. [1 ]
Chan, Catherine B. [1 ,2 ]
Willing, Benjamin P. [1 ]
机构
[1] Univ Alberta, Dept Agr Food & Nutr Sci, Edmonton, AB T6G 2P5, Canada
[2] Univ Alberta, Dept Physiol, Edmonton, AB T6G 2H7, Canada
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
INTESTINAL ALKALINE-PHOSPHATASE; CHAIN FATTY-ACIDS; PROTEIN-COUPLED RECEPTOR; BETA-CELL PROLIFERATION; HUMAN GUT MICROBIOTA; CHILDHOOD OVERWEIGHT; POSTNATAL-GROWTH; OBESITY; PERTURBATION; APOPTOSIS;
D O I
10.1038/srep41778
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Childhood antibiotic exposure has been recently linked with increased risk of metabolic disease later in life. A better understanding of this association would potentially provide strategies to reduce the childhood chronic disease epidemic. Therefore, we explored the underlying mechanisms using a swine model that better mimics human infants than rodents, and demonstrated that early life antibiotic exposure affects glucose metabolism 5 weeks after antibiotic withdrawal, which was associated with changes in pancreatic development. Antibiotics exerted a transient impact on postnatal gut microbiota colonization and microbial metabolite production, yet changes in the expression of key genes involved in short-chain fatty acid signaling and pancreatic development were detected in later life. These findings suggest a programming effect of early life antibiotic exposure that merits further investigation.
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页数:12
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