An Additive Effect of Promoting Thermogenic Gene Expression in Mice Adipose-Derived Stromal Vascular Cells by Combination of Rosiglitazone and CL316,243

It is well-documented that CL316,243 (a β3 agonist) or rosiglitazone (a PPARγ agonist) can induce white adipocyte populations to brown-like adipocytes, thus increasing energy consumption and combating obesity. However, whether there is a combined effect remains unknown. In the present study, stromal...

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Veröffentlicht in:International journal of molecular sciences 2017-05, Vol.18 (5), p.1002
Hauptverfasser: Li, You-Lei, Li, Xiao, Jiang, Tian-Tuan, Fan, Jia-Min, Zheng, Xue-Li, Shi, Xin-E, Yu, Tai-Yong, Chu, Gui-Yan, Yang, Gong-She
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Sprache:eng
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Zusammenfassung:It is well-documented that CL316,243 (a β3 agonist) or rosiglitazone (a PPARγ agonist) can induce white adipocyte populations to brown-like adipocytes, thus increasing energy consumption and combating obesity. However, whether there is a combined effect remains unknown. In the present study, stromal vascular cells of inguinal white adipose tissue (iWAT-SVCs for short) from mice were cultured and induced into browning by CL316,243, rosiglitazone, or both. Results showed that a combination of CL316,243 and rosiglitazone significantly upregulated the expression of the core thermogenic gene as well as genes related with mitochondrial function ( , , , , and ), compared with the treatment of CL316,243 or rosiglitazone alone. Moreover, co-treatment with rosiglitazone could reverse the downregulation of resulting from CL316,243 stimuli alone. Taken together, a combination of rosiglitazone and CL316,243 can produce an additive effect of promoting thermogenic gene expression and an improvement of insulin sensitivity in mouse iWAT-SVCs.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms18051002