Oh Chang-Myung, Namkung Jun, Go Younghoon, Shong Ko Eun, Kim Kyuho, Kim Hyeongseok, Park Bo-Yoon, Lee Ho Won, Jeon Yong Hyun, Song Junghan, Shong Minho, Yadav Vijay K, Karsenty Gerard, Kajimura Shingo, Lee In-Kyu, Park Sangkyu, Kim Hail
BioMedical Research Center (E7) 8104, Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon 305-701, Korea.
Department of Biochemistry, Yonsei University Wonju College of Medicine, Wonju 220-701, Korea.
Nat Commun. 2015 Apr 13;6:6794. doi: 10.1038/ncomms7794.
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.
中枢5-羟色胺(5-HT)是大脑中的一种厌食性神经递质。然而,越来越多的证据表明外周5-HT可能会影响机体的能量稳态。在此我们表明5-HT可调节白色和棕色脂肪组织的功能。对5-HT合成进行药理抑制会导致附睾白色脂肪组织(WAT)中脂肪生成受到抑制,腹股沟WAT发生褐变以及棕色脂肪组织(BAT)中适应性产热被激活。脂肪组织中可诱导性Tph1基因敲除的小鼠表现出与通过药物抑制5-HT合成的小鼠相似的表型,这表明5-HT对脂肪组织具有局部作用。此外,Htr3a基因敲除小鼠在喂食高脂饮食时能量消耗增加且体重增加减少。用Htr2a拮抗剂进行处理可减少3T3-L1脂肪细胞中的脂质积累。这些数据表明脂肪细胞源性5-HT在控制能量稳态中具有重要作用。