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UA-mediated thermogenesis and body weight control in mice is preserved at thermoneutrality.

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posted on 2020-03-27, 17:34 authored by Bo Xia, Xiao Chen Shi, Bao Cai Xie, Meng Qing Zhu, Yan Chen, Xin Yi Chu, Guo He Cai, Min Liu, Shi Zhen Yang, Grant A. Mitchell, Wei Jun Pang, Jiang Wei Wu

(A) Schematic diagram of mice treatment. (B) Body weight of HFD-fed mice treated with UA or vehicle at 30°C (n = 6). (C) Daily food intake of mice at 30°C (n = 6). (D) Body composition measured by DEXA scan after 6 weeks of treatment. (E) Oxygen consumption of mice tested for 24 h (n = 6). (F) The body temperature of mice at 30°C (n = 6). (G) Representative infrared images of the vehicle and UA-treated mice. mRNA levels of thermogenic genes in (H) iWAT and (I) BAT from UA-treated or vehicle control mice at 30°C (n = 6). (J) NE-stimulated whole-body oxygen consumption in UA-treated mice and controls mice at 30°C. (K) mRNA levels of thermogenic genes in denervated BAT of UA-treated or vehicle mice at room temperature. The underlying data for this figure can be found in S1 Data. BAT, brown adipose tissue; Cox7a, Cytochrome c oxidase subunit 7a1; DEXA, dual-energy X-ray absorptiometry; Dio2, Deiodinase 2; HFD, high-fat diet; iWAT, inguinal white adipose tissue; NE, norepinephrine; Pgc1-α, Peroxisome proliferator-activated receptor gamma coactivator 1α; UA, urolithin A; Ucp1, Uncoupling protein 1.

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