Regulation of systemic energy homeostasis by serotonin in adipose tissues

Chang‐Myung Oh(Korea Advanced Institute of Science and Technology), Jun Namkung(Korea Advanced Institute of Science and Technology), Younghoon Go(Kyungpook National University Hospital), Ko Eun Shong(Korea Advanced Institute of Science and Technology), Kyuho Kim(Korea Advanced Institute of Science and Technology), Hyeongseok Kim(Korea Advanced Institute of Science and Technology), Bo-Yoon Park(Kyungpook National University Hospital), Ho‐Won Lee(Kyungpook National University Hospital), Yong Hyun Jeon(Kyungpook National University Hospital), Junghan Song(Seoul National University Bundang Hospital), Minho Shong(Chungnam National University), Vijay K. Yadav(Wellcome Sanger Institute), Gérard Karsenty(Columbia University Irving Medical Center), Shingo Kajimura(University of California, San Francisco), In‐Kyu Lee(Kyungpook National University Hospital), Sangkyu Park(Korea Advanced Institute of Science and Technology), Hail Kim(Korea Advanced Institute of Science and Technology)
Nature Communications
April 13, 2015
Cited by 260Open Access
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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.


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