Haahr M E, Hansen D L, Fisher P M, Svarer C, Stenbæk D S, Madsen K, Madsen J, Holst J J, Baaré W F C, Hojgaard L, Almdal T, Knudsen G M
Neurobiology Research Unit, Rigshospitalet, 2100 Copenhagen, Denmark, Center for Integrated Molecular Brain Imaging, Rigshospitalet and University of Copenhagen, 2100 Copenhagen, Denmark.
Department of Endocrinology and.
J Neurosci. 2015 Apr 8;35(14):5884-9. doi: 10.1523/JNEUROSCI.3348-14.2015.
The cerebral serotonin (5-HT) system shows distinct differences in obesity compared with the lean state. Here, it was investigated whether serotonergic neurotransmission in obesity is a stable trait or changes in association with weight loss induced by Roux-in-Y gastric bypass (RYGB) surgery. In vivo cerebral 5-HT2A receptor and 5-HT transporter binding was determined by positron emission tomography in 21 obese [four men; body mass index (BMI), 40.1 ± 4.1 kg/m(2)] and 10 lean (three men; BMI, 24.6 ± 1.5 kg/m(2)) individuals. Fourteen obese individuals were re-examined after RYGB surgery. First, it was confirmed that obese individuals have higher cerebral 5-HT2A receptor binding than lean individuals. Importantly, we found that higher presurgical 5-HT2A receptor binding predicted greater weight loss after RYGB and that the change in 5-HT2A receptor and 5-HT transporter binding correlated with weight loss after RYGB. The changes in the 5-HT neurotransmission before and after RYGB are in accordance with a model wherein the cerebral extracellular 5-HT level modulates the regulation of body weight. Our findings support that the cerebral 5-HT system contributes both to establish the obese condition and to regulate the body weight in response to RYGB.
与瘦的状态相比,大脑血清素(5-羟色胺,5-HT)系统在肥胖状态下表现出明显差异。在此,研究了肥胖状态下的血清素能神经传递是一种稳定特征,还是会随着Roux-en-Y胃旁路术(RYGB)手术引起的体重减轻而发生变化。通过正电子发射断层扫描确定了21名肥胖者[4名男性;体重指数(BMI),40.1±4.1kg/m²]和10名瘦者(3名男性;BMI,24.6±1.5kg/m²)体内大脑5-HT2A受体和5-HT转运体的结合情况。14名肥胖者在RYGB手术后接受了复查。首先,证实肥胖者大脑5-HT2A受体结合高于瘦者。重要的是,我们发现术前较高的5-HT2A受体结合预示着RYGB术后体重减轻更多,并且5-HT2A受体和5-HT转运体结合的变化与RYGB术后体重减轻相关。RYGB手术前后5-HT神经传递的变化符合一种模型,即大脑细胞外5-HT水平调节体重的调控。我们的研究结果支持大脑5-HT系统既有助于形成肥胖状态,也有助于响应RYGB调节体重。