Literature DB >> 30708100

Linifanib exerts dual anti-obesity effect by regulating adipocyte browning and formation.

Shiting Zhao1, Yi Chu2, Yuwei Zhang3, Yulai Zhou4, Zhiwu Jiang2, Zhengqi Wang5, Liufeng Mao2, Kuai Li2, Wei Sun2, Peng Li2, Shiqi Jia5, Cunchuan Wang5, Aimin Xu6, Kerry Loomes7, Shibing Tang2, Donghai Wu2, Xiaoyan Hui8, Tao Nie9.   

Abstract

Obesity is caused by energy imbalance and accompanied by adipocyte hypertrophy and hyperplasia. Therefore, both enhancement of adipocyte energy expenditure and inhibition of adipogenesis are viable ways to combat obesity. Using the Ucp1-2A-luciferase reporter animal model previously reported by us as a screening platform, a chemical compound Linifanib was identified as a potent inducer of UCP1 expression in primary inguinal adipocytes in vitro and in vivo. Signal pathway analyses showed that Linifanib promoted adipocyte browning by attenuating STAT3 phosphorylation. The effects of Linifanib on adipocyte browning were blocked by the compound, SD19, which activates the STAT3 signaling cascade. Linifanib also inhibited adipocyte differentiation, by blocking mitotic clonal expansion, which could be rescued by STAT3 activator. Taken together, our results indicate that Linifanib might serve as a potential drug for the treatment of obesity.
Copyright © 2019. Published by Elsevier Inc.

Entities:  

Keywords:  Adipogenesis; Browning; Linifanib; Obesity; STAT3

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Year:  2019        PMID: 30708100     DOI: 10.1016/j.lfs.2019.01.047

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  1 in total

1.  Pharmacological modulation of RORα controls fat browning, adaptive thermogenesis, and body weight in mice.

Authors:  Martine Auclair; Natacha Roblot; Emilie Capel; Bruno Fève; Bénédicte Antoine
Journal:  Am J Physiol Endocrinol Metab       Date:  2020-11-30       Impact factor: 4.310

  1 in total

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