FXR-deficiency confers increased susceptibility to torpor.

Abstract : The role of the nuclear receptor FXR in adaptive thermogenesis was investigated using FXR-deficient mice. Despite elevated serum bile acid concentrations and increased mRNA expression profiles of thermogenic genes in brown adipose tissue, FXR-deficiency did not alter energy expenditure under basal conditions. However, FXR-deficiency accelerated the fasting-induced entry into torpor in a leptin-dependent manner. FXR-deficient mice were also extremely cold-intolerant. These altered responses may be linked to a more rapid decrease in plasma concentrations of metabolic fuels (glucose, triglycerides) thus impairing uncoupling protein 1-driven thermogenesis. These results identify FXR as a modulator of energy homeostasis.
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FEBS Letters, Wiley, 2007, 581 (27), pp.5191-8. 〈10.1016/j.febslet.2007.09.064〉
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Soumis le : lundi 10 août 2009 - 15:01:18
Dernière modification le : mercredi 25 juillet 2018 - 10:52:02

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Bertrand Cariou, Emmanuel Bouchaert, Mouaadh Abdelkarim, Julie Dumont, Sandrine Caron, et al.. FXR-deficiency confers increased susceptibility to torpor.. FEBS Letters, Wiley, 2007, 581 (27), pp.5191-8. 〈10.1016/j.febslet.2007.09.064〉. 〈inserm-00409558〉

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