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Regulation of systemic energy homeostasis by serotonin in adipose tissues.
- Source :
-
Nature communications [Nat Commun] 2015 Apr 13; Vol. 6, pp. 6794. Date of Electronic Publication: 2015 Apr 13. - Publication Year :
- 2015
-
Abstract
- Central serotonin (5-HT) is an anorexigenic neurotransmitter in the brain. However, accumulating evidence suggests peripheral 5-HT may affect organismal energy homeostasis. Here we show 5-HT regulates white and brown adipose tissue function. Pharmacological inhibition of 5-HT synthesis leads to inhibition of lipogenesis in epididymal white adipose tissue (WAT), induction of browning in inguinal WAT and activation of adaptive thermogenesis in brown adipose tissue (BAT). Mice with inducible Tph1 KO in adipose tissues exhibit a similar phenotype as mice in which 5-HT synthesis is inhibited pharmacologically, suggesting 5-HT has localized effects on adipose tissues. In addition, Htr3a KO mice exhibit increased energy expenditure and reduced weight gain when fed a high-fat diet. Treatment with an Htr2a antagonist reduces lipid accumulation in 3T3-L1 adipocytes. These data suggest important roles for adipocyte-derived 5-HT in controlling energy homeostasis.
- Subjects :
- 3T3-L1 Cells
Adipocytes, Brown metabolism
Adipocytes, Brown pathology
Adipocytes, White metabolism
Adipocytes, White pathology
Adipose Tissue, Brown pathology
Adipose Tissue, White pathology
Animals
Diet, High-Fat
Energy Metabolism genetics
Epididymis metabolism
Epididymis pathology
Gene Expression
Male
Mice
Mice, Knockout
Obesity etiology
Obesity pathology
Receptor, Serotonin, 5-HT2A genetics
Receptor, Serotonin, 5-HT2A metabolism
Receptors, Serotonin, 5-HT3 deficiency
Receptors, Serotonin, 5-HT3 genetics
Thermogenesis genetics
Tryptophan Hydroxylase deficiency
Tryptophan Hydroxylase genetics
Adipogenesis genetics
Adipose Tissue, Brown metabolism
Adipose Tissue, White metabolism
Homeostasis genetics
Obesity metabolism
Serotonin metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 6
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 25864946
- Full Text :
- https://doi.org/10.1038/ncomms7794