Jakobsen Gustav R, Fisher Patrick M, Dyssegaard Agnete, McMahon Brenda, Holst Klaus K, Lehel Szabolcs, Svarer Claus, Jensen Peter S, Knudsen Gitte M, Frokjaer Vibe G
Neurobiology Research Unit and Center for Integrated Molecular Brain Imaging, DK-2100 Copenhagen, Denmark; Faculty of Health and Medical Sciences, University of Copenhagen, DK-2100 Copenhagen, Denmark.
Neurobiology Research Unit and Center for Integrated Molecular Brain Imaging, DK-2100 Copenhagen, Denmark.
Psychoneuroendocrinology. 2016 May;67:124-32. doi: 10.1016/j.psyneuen.2016.01.032. Epub 2016 Feb 11.
Serotonin signalling is considered critical for an appropriate and dynamic adaptation to stress. Previously, we have shown that prefrontal serotonin transporter (SERT) binding is positively associated with the cortisol awakening response (CAR) (Frokjaer et al., 2013), which is an index of hypothalamic-pituitary-adrenal (HPA)-axis output dynamics. Here, we investigated in healthy individuals if cerebral serotonin 4 receptor (5-HT4r) binding, reported to be a proxy for serotonin levels, is associated with CAR. Thirty healthy volunteers (25 males, age range 20-56 years) underwent 5-HT4r PET imaging with [(11)C]-SB207145, genotyping of the SERT-linked polymorphic region (5-HTTLPR), and performed serial home sampling of saliva (5 time points from 0 to 60min from awakening) to assess CAR. The association between 5-HT4r binding in 4 regions of interest (prefrontal cortex, anterior cingulate cortex, pallidostriatum, and hippocampus) and CAR was tested using multiple linear regression with adjustment for age and 5-HTTLPR genotype. Finally, an exploratory voxel-based analysis of the association was performed. CAR was negatively associated with 5-HT4r binding in pallidostriatum (p=0.01), prefrontal cortex (p=0.03), and anterior cingulate cortex (p=0.002), respectively, but showed no association in hippocampus. The results remained significant when taking into account other potentially relevant covariates. In conclusion, our finding reinforces an association between HPA-axis function and serotonin signaling in vivo in humans. We suggest that higher synaptic serotonin concentration, here indexed by lower 5-HT4r binding, supports HPA-axis dynamics, which in healthy volunteers is reflected by a robust CAR.
血清素信号传导被认为对于适当且动态地适应压力至关重要。此前,我们已经表明前额叶血清素转运体(SERT)结合与皮质醇觉醒反应(CAR)呈正相关(Frokjaer等人,2013年),而皮质醇觉醒反应是下丘脑 - 垂体 - 肾上腺(HPA)轴输出动态的一个指标。在此,我们在健康个体中研究了据报道可作为血清素水平替代指标的脑血清素4受体(5-HT4r)结合是否与CAR相关。30名健康志愿者(25名男性,年龄范围20 - 56岁)接受了用[(11)C]-SB207145进行的5-HT4r正电子发射断层扫描(PET)成像、血清素转运体相关多态性区域(5-HTTLPR)的基因分型,并进行了唾液的系列家庭采样(从觉醒开始0至60分钟内的5个时间点)以评估CAR。使用多元线性回归并对年龄和5-HTTLPR基因型进行校正,测试了4个感兴趣区域(前额叶皮质、前扣带回皮质、苍白球纹状体和海马体)中的5-HT4r结合与CAR之间的关联。最后,对该关联进行了基于体素的探索性分析。CAR分别与苍白球纹状体(p = 0.01)、前额叶皮质(p = 0.03)和前扣带回皮质(p = 0.002)中的5-HT4r结合呈负相关,但在海马体中未显示出相关性。在考虑其他潜在相关协变量时,结果仍然显著。总之,我们的发现强化了人类体内HPA轴功能与血清素信号传导之间的关联。我们认为,在此由较低的5-HT4r结合所表征的较高突触血清素浓度支持了HPA轴动态,这在健康志愿者中表现为强烈的CAR。