首页> 美国卫生研究院文献>The Journal of Neuroscience >The Activity-Regulated Cytoskeletal-Associated Protein (Arc/Arg3.1) Is Required for Memory Consolidation of Pavlovian Fear Conditioning in the Lateral Amygdala
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The Activity-Regulated Cytoskeletal-Associated Protein (Arc/Arg3.1) Is Required for Memory Consolidation of Pavlovian Fear Conditioning in the Lateral Amygdala

机译:活动调节的细胞骨架相关蛋白(Arc / Arg3.1)是杏仁核外侧巴甫洛夫恐惧调理的记忆巩固所必需的。

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摘要

The activity-regulated cytoskeletal-associated protein (Arc/Arg3.1) is an immediate early gene that has been widely implicated in hippocampal-dependent learning and memory and is believed to play an integral role in synapse-specific plasticity. Here, we examined the role of Arc/Arg3.1 in amygdala-dependent Pavlovian fear conditioning. We first examined the regulation of Arc/Arg3.1 mRNA and protein after fear conditioning and LTP-inducing stimulation of thalamic inputs to the lateral amygdala (LA). Quantitative real-time PCR, in situ hybridization, Western blotting and immunohistochemistry revealed a significant upregulation of Arc/Arg3.1 mRNA and protein in the LA relative to controls. In behavioral experiments, intra-LA infusion of an Arc/Arg3.1 antisense oligodeoxynucleotide (ODN) was observed to be anatomically restricted to the LA, taken up by LA cells, and to promote significant knockdown of Arc/Arg3.1 protein. Rats given intra-LA infusions of multiple doses of the Arc/Arg3.1 ODN showed an impairment of LTM (tested ∼24 later), but no deficit in STM (tested 3 h later) relative to controls infused with scrambled ODN. Finally, to determine whether upregulation of Arc/Arg3.1 occurs downstream of ERK/MAPK activation, we examined Arc/Arg3.1 expression in rats given intra-LA infusion of the MEK inhibitor U0126. Relative to vehicle controls, infusion of U0126 impaired training-induced increases in Arc/Arg3.1 expression. These findings suggest that Arc/Arg3.1 expression in the amygdala is required for fear memory consolidation, and further suggest that Arc/Arg3.1 regulation in the LA is downstream of the ERK/MAPK signaling pathway.
机译:活性调节的细胞骨架相关蛋白(Arc / Arg3.1)是一个直接的早期基因,已广泛参与海马依赖性学习和记忆,并被认为在突触特异性可塑性中起着不可或缺的作用。在这里,我们检查了Arc / Arg3.1在依赖杏仁核的巴甫洛夫式恐惧条件中的作用。我们首先检查恐惧条件和LTP诱导丘脑输入到外侧杏仁核(LA)后刺激Arc / Arg3.1 mRNA和蛋白质的调节。定量实时PCR,原位杂交,Western印迹和免疫组织化学分析显示,相对于对照,LA中Arc / Arg3.1 mRNA和蛋白的显着上调。在行为实验中,观察到LA / Arc3.1反义寡聚脱氧核苷酸(ODN)的LA内输注在解剖学上仅限于LA,被LA细胞吸收,并促进了Arc / Arg3.1蛋白的显着敲低。相对于注入了扰乱的ODN的对照组,接受多剂量Arc / Arg3.1 ODN的LA内输注的大鼠显示LTM受损(约24小时后测试),但STM无缺陷(3h后测试)。最后,为了确定Arc / Arg3.1的上调是否发生在ERK / MAPK激活的下游,我们检查了在LA内输注MEK抑制剂U0126的大鼠中Arc / Arg3.1的表达。相对于车辆控制,U0126的输注削弱了训练诱导的Arc / Arg3.1表达的增加。这些发现表明杏仁核中的Arc / Arg3.1表达是恐惧记忆巩固所必需的,并且进一步表明LA中的Arc / Arg3.1调控是ERK / MAPK信号通路的下游。

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