Brown adipose tissue is the key depot for glucose clearance in microbiota depleted mice

Author:

Li Min,Li LiORCID,Li Baoguo,Hambly Catherine,Wang Guanlin,Wu Yingga,Jin Zengguang,Wang Anyongqi,Niu Chaoqun,Wolfrum ChristianORCID,Speakman John R.ORCID

Abstract

AbstractGut microbiota deficient mice demonstrate accelerated glucose clearance. However, which tissues are responsible for the upregulated glucose uptake remains unresolved, with different studies suggesting that browning of white adipose tissue, or modulated hepatic gluconeogenesis, may be related to enhanced glucose clearance when the gut microbiota is absent. Here, we investigate glucose uptake in 22 different tissues in 3 different mouse models. We find that gut microbiota depletion via treatment with antibiotic cocktails (ABX) promotes glucose uptake in brown adipose tissue (BAT) and cecum. Nevertheless, the adaptive thermogenesis and the expression of uncoupling protein 1 (UCP1) are dispensable for the increased glucose uptake and clearance. Deletion of Ucp1 expressing cells blunts the improvement of glucose clearance in ABX-treated mice. Our results indicate that BAT and cecum, but not white adipose tissue (WAT) or liver, contribute to the glucose uptake in the gut microbiota depleted mouse model and this response is dissociated from adaptive thermogenesis.

Funder

National Science Foundation of China | National Natural Science Foundation of China-Yunnan Joint Fund

KC Wong Education Foundation ‘1000 talents’ recruitment program PIFI professorial fellowship from CAS Wolfson merit professorship from the UK Royal Society

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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