首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Single prolonged stress increases contextual freezing and the expression of glycine transporter 1 and vesicle-associated membrane protein 2 mRNA in the hippocampus of rats.
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Single prolonged stress increases contextual freezing and the expression of glycine transporter 1 and vesicle-associated membrane protein 2 mRNA in the hippocampus of rats.

机译:长时间的单一应激会增加大鼠海马的环境冻结和甘氨酸转运蛋白1和囊泡相关膜蛋白2 mRNA的表达。

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摘要

Rats subjected to single prolonged stress (SPS) show enhanced HPA negative feedback, exaggerated acoustic startle response, and enhanced contextual freezing 7 days after SPS, and accordingly, SPS is an animal model of PTSD. To elucidate the influence of contextual fear on gene expression in the hippocampus of SPS rats, we used cDNA microarray followed by real-time quantitative PCR analyses to compare the hippocampal gene expression profiles between rats that were or were not subjected to SPS during exposure to contextual fear. In the behavioral experiments, spontaneous locomotor activity was measured 7 days after SPS. Twenty-four hours after footshock conditioning (7 days after SPS), freezing behavior was measured during re-exposure to the chamber in which footshock was delivered. Based on the behavioral analysis, rats subjected to SPS exhibited a significant enhancement of contextual freezing compared to rats not subjected to SPS, without any changes in locomotor activity. Analyses using cDNA microarray and RT-PCR showed that the hippocampal levels of glycine transporter 1 (Gly-T1) and vesicle-associated membrane protein 2 (VAMP2) mRNA in rats subjected to SPS were significantly increased relative to sham-treated rats. Administration of SPS alone did not affect the expression of these 2 genes. These findings suggest that the upregulation of Gly-T1 and VAMP2 in the hippocampus may be, at least in part, involved in the enhanced susceptibility to contextual fear in rats subjected to SPS.
机译:遭受单次长时间应激(SPS)的大鼠在SPS后7天显示出增强的HPA负反馈,夸张的听觉惊吓反应和增强的情景冻结,因此,SPS是PTSD的动物模型。为了阐明情境恐惧对SPS大鼠海马基因表达的影响,我们使用cDNA芯片,然后进行实时定量PCR分析,比较暴露于情境中或未遭受SPS的大鼠之间海马基因表达谱恐惧。在行为实验中,SPS 7天后测量自发运动能力。进行休克后24小时(SPS后7天),在再次暴露于递送休克的房间中测量了冰冻行为。根据行为分析,与未接受SPS的大鼠相比,接受SPS的大鼠表现出明显的环境冻结,运动能力没有任何变化。使用cDNA芯片和RT-PCR进行的分析表明,与假手术大鼠相比,SPS大鼠海马中的甘氨酸转运蛋白1(Gly-T1)和囊泡相关膜蛋白2(VAMP2)mRNA的水平显着增加。单独施用SPS不会影响这两个基因的表达。这些发现表明,海马中Gly-T1和VAMP2的上调可能至少部分参与了遭受SPS的大鼠对背景恐惧的敏感性增强。

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