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Elucidation of the roles of brown and brite fat genes: GPR120 is a modulator of brown adipose tissue function.

Mark Christian
Published in: Experimental physiology (2020)
The identification of druggable targets to stimulate brown adipose tissue (BAT) is a strategy to combat obesity due to this highly metabolically active tissue utilising thermogenesis to burn fat. Upon cold exposure BAT is activated by the sympathetic nervous system via β3 -adrenergic receptors. Determination of additional receptors expressed by brown, white and brite (brown-in-white) fat can lead to new pharmacological treatments to activate BAT. GPR120 is a G protein-coupled fatty acid receptor that is highly expressed in BAT and further increases in response to cold. Activation of this receptor with the selective agonist TUG-891 acutely increases fat oxidation and reduces fat mass in mice. The effects are coincident with increased BAT activity and enhanced nutrient uptake. TUG-891 stimulation of brown adipocytes induces intracellular Ca2+ release which results in elevated O2 consumption as well as mitochondrial depolarisation and fission. Thus, activation of GPR120 in BAT with ligands such as TUG-891 is a promising strategy to increase fat consumption.
Keyphrases
  • adipose tissue
  • fatty acid
  • insulin resistance
  • high fat diet
  • high fat diet induced
  • type diabetes
  • oxidative stress
  • genome wide
  • reactive oxygen species
  • mass spectrometry
  • wound healing
  • genome wide analysis