Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, United Kingdom
Behavioral and Clinical Neuroscience Institute, University of Cambridge, Cambridge CB2 3EB, United Kingdom.
J Neurosci. 2020 Jun 10;40(24):4739-4749. doi: 10.1523/JNEUROSCI.2930-19.2020. Epub 2020 May 11.
High trait anxiety is associated with altered activity across emotion regulation circuitry and a higher risk of developing anxiety disorders and depression. This circuitry is extensively modulated by serotonin. Here, to understand why some people may be more vulnerable to developing affective disorders, we investigated whether serotonin-related gene expression across the brain's emotion regulation circuitry may underlie individual differences in trait anxiety using the common marmoset (, mixed sexes) as a model. First, we assessed the association of region-specific expression of the serotonin transporter () and serotonin receptor (, , ) genes with anxiety-like behavior; and second, we investigated their causal role in two key features of the high trait anxious phenotype: high responsivity to anxiety-provoking stimuli and an exaggerated conditioned threat response. While the expression of the serotonin receptors did not show a significant relationship with anxiety-like behavior in any of the targeted brain regions, serotonin transporter expression, specifically within the right ventrolateral prefrontal cortex (vlPFC) and most strongly in the right amygdala, was associated positively with anxiety-like behavior. The causal relationship between amygdala serotonin levels and an animal's sensitivity to threat was confirmed via direct amygdala infusions of a selective serotonin reuptake inhibitor (SSRI), citalopram. Both anxiety-like behaviors, and conditioned threat-induced responses were reduced by the blockade of serotonin reuptake in the amygdala. Together, these findings provide evidence that high amygdala serotonin transporter expression contributes to the high trait anxious phenotype and suggest that reduction of threat reactivity by SSRIs may be mediated by their actions in the amygdala. Findings here contribute to our understanding of how the serotonin system underlies an individual's expression of threat-elicited negative emotions such as anxiety and fear within nonhuman primates. Exploration of serotonergic gene expression across brain regions implicated in emotion regulation revealed that serotonin transporter gene expression in the ventrolateral prefrontal cortex (vlPFC) and most strongly in the amygdala, but none of the serotonin receptor genes, were predictive of interindividual differences in anxiety-like behavior. Targeting of amygdala serotonin reuptake with selective serotonin reuptake inhibitors (SSRIs) confirmed the causal relationship between amygdala serotonin transporter and an animal's sensitivity to threat by reversing expression of two key features of the high trait-like anxiety phenotype: high responsivity to anxiety-provoking uncertain threat and responsivity to certain conditioned threat.
高特质焦虑与情绪调节回路中活动的改变有关,并且患焦虑症和抑郁症的风险更高。该回路广泛受 5-羟色胺调节。在这里,为了了解为什么有些人可能更容易患上情感障碍,我们使用普通狨猴(雌雄混合)作为模型,研究了大脑情绪调节回路中与 5-羟色胺相关的基因表达是否会导致特质焦虑的个体差异。首先,我们评估了特定于区域的 5-羟色胺转运体()和 5-羟色胺受体(、、)基因表达与焦虑样行为之间的关联;其次,我们研究了它们在高特质焦虑表型的两个关键特征中的因果作用:对引起焦虑的刺激的高反应性和对夸大的条件性威胁的反应。虽然在任何靶向脑区中,5-羟色胺受体的表达与焦虑样行为之间都没有显著的关系,但 5-羟色胺转运体的表达,特别是在右侧腹外侧前额叶皮层(vlPFC)和右侧杏仁核中,与焦虑样行为呈正相关。通过直接向杏仁核内输注选择性 5-羟色胺再摄取抑制剂(SSRI)西酞普兰,证实了杏仁核内 5-羟色胺水平与动物对威胁的敏感性之间的因果关系。阻断杏仁核内的 5-羟色胺再摄取,既可以减少焦虑样行为,又可以减少条件性威胁诱导的反应。总之,这些发现提供了证据,表明高杏仁核 5-羟色胺转运体表达有助于高特质焦虑表型,并表明 SSRI 通过其在杏仁核中的作用降低威胁反应。这些发现有助于我们理解在非人类灵长类动物中,5-羟色胺系统如何导致个体表达与威胁相关的负面情绪,如焦虑和恐惧。对涉及情绪调节的脑区中 5-羟色胺能基因表达的探索表明,在腹外侧前额叶皮层(vlPFC)和杏仁核中,5-羟色胺转运体基因表达最强,但 5-羟色胺受体基因均不预测焦虑样行为的个体差异。使用选择性 5-羟色胺再摄取抑制剂(SSRIs)靶向杏仁核 5-羟色胺再摄取,通过逆转高特质焦虑样表型的两个关键特征的表达,证实了杏仁核 5-羟色胺转运体与动物对威胁的敏感性之间的因果关系:对引起焦虑的不确定威胁的高反应性和对特定条件性威胁的反应性。