†Donders Institute for Brain, Cognition and Behaviour, Centre for Neuroscience, Department of Cognitive Neuroscience, and ‡Donders Institute for Brain, Cognition and Behaviour, Centre for Neuroscience, Department of Anatomy, Radboud University Medical Centre, Geert Grooteplein 21, 6525 EZ Nijmegen, The Netherlands.
ACS Chem Neurosci. 2015 Jul 15;6(7):1143-50. doi: 10.1021/acschemneuro.5b00126. Epub 2015 Jul 6.
Variations in serotonin transporter (5-HTT) expression have been associated with altered sensitivity to stress. Since controllability is known to alter the impact of a stressor through differential activation of the medial prefrontal cortex (mPFC) and dorsal raphe nucleus (DRN), and that these regions are functionally affected by genetic 5-HTT down-regulation, we hypothesized that 5-HTT expression modulates the effect of controllability on stressor impact and coping. Here, we investigated the effects of a signaled stress controllability task or a yoked uncontrollable stressor on behavioral responding and mPFC and DRN activation. 5-HTT(-/-) rats proved better capable of acquiring the active avoidance task than 5-HTT(+/+) animals. Controllability determined DRN activation in 5-HTT(+/+), but not 5-HTT(-/-), rats, whereas controllability-related activation of the mPFC was independent of genotype. These findings suggest that serotonergic activation in the DRN is involved in stress coping in a 5-HTT expression dependent manner, whereas mPFC activation seems to be implicated in control over stress independently of 5-HTT expression. We speculate that alterations in serotonergic feedback in the DRN might be a potential mechanism driving this differential stress coping.
5-羟色胺转运体(5-HTT)表达的变化与对压力的敏感性改变有关。由于控制能力已知通过内侧前额叶皮层(mPFC)和中缝背核(DRN)的差异激活改变应激源的影响,并且这些区域受到遗传 5-HTT 下调的功能影响,我们假设 5-HTT 表达调节可控性对压力源影响和应对的影响。在这里,我们研究了信号应激可控性任务或偶联不可控应激源对行为反应和 mPFC 和 DRN 激活的影响。5-HTT(-/-)大鼠比 5-HTT(+/+)动物更能成功地完成主动回避任务。在 5-HTT(+/+)大鼠中,可控性决定了 DRN 的激活,但在 5-HTT(-/-)大鼠中则没有,而与可控性相关的 mPFC 激活则与基因型无关。这些发现表明,DRN 中的 5-羟色胺能激活以 5-HTT 表达依赖性的方式参与应激应对,而 mPFC 的激活似乎与 5-HTT 表达无关,参与对压力的控制。我们推测,DRN 中 5-羟色胺能反馈的改变可能是驱动这种不同的应激应对的潜在机制。