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Depletion of serotonin in the basolateral amygdala elevates glutamate receptors and facilitates fear-potentiated startle

机译:基底外侧杏仁核中5-羟色胺的减少会增加谷氨酸受体并促进恐惧增强的惊吓

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摘要

Our previous experiments demonstrated that systemic depletion of serotonin (5-hydroxytryptamine, 5-HT), similar to levels reported in patients with emotional disorders, enhanced glutamateric activity in the lateral nucleus of the amygdala (LA) and potentiated fear behaviors. However, the effects of isolated depletion of 5-HT in the LA, and the molecular mechanisms underlying enhanced glutamatergic activity are unknown. In the present study, we tested the hypothesis that depletion of 5-HT in the LA induces increased fear behavior, and concomitantly enhances glutamate receptor (GluR) expression. Bilateral infusions of 5,7-dihydroxytryptamine (4 μg per side) into the LA produced a regional reduction of serotonergic fibers, resulting in decreased 5-HT concentrations. The induction of low 5-HT in the LA elevated fear-potentiated startle, with a parallel increase in GluR1 mRNA and GluR1 protein expression. These findings suggest that low 5-HT concentrations in the LA may facilitate fear behavior through enhanced GluR-mediated mechanisms. Moreover, our data support a relationship between 5-HT and glutamate in psychopathologies.
机译:我们以前的实验表明,5-羟色胺(5-羟色胺,5-HT)的全身消耗与情绪障碍患者中报道的水平相似,杏仁核(LA)外侧核的谷氨酸活性增强,并增强了恐惧行为。然而,未知的洛杉矶5-HT的单独消耗的影响,以及增强谷氨酸能活性的分子机制尚不清楚。在本研究中,我们测试了以下假设:洛杉矶中5-HT的消耗诱导恐惧行为增加,并同时增强谷氨酸受体(GluR)的表达。向洛杉矶双侧输注5,7-二羟基色胺(每侧4μg)会导致5-羟色胺能纤维的区域减少,从而导致5-HT浓度降低。洛杉矶地区低5-HT的诱导升高了恐惧增强的惊吓,同时GluR1 mRNA和GluR1蛋白表达平行增加。这些发现表明,洛杉矶地区5-HT浓度低可能通过增强的GluR介导的机制促进恐惧行为。此外,我们的数据支持5-HT和谷氨酸在精神病理学之间的关系。

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