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促进 AMPA 受体突触传递作为认知增强的分子机制。

Facilitation of AMPA receptor synaptic delivery as a molecular mechanism for cognitive enhancement.

机构信息

Centro de Biología Molecular "Severo Ochoa," Consejo Superior de Investigaciones Científicas (CSIC)/Universidad Autónoma de Madrid, Madrid, Spain.

出版信息

PLoS Biol. 2012 Feb;10(2):e1001262. doi: 10.1371/journal.pbio.1001262. Epub 2012 Feb 21.

Abstract

Cell adhesion molecules and downstream growth factor-dependent signaling are critical for brain development and synaptic plasticity, and they have been linked to cognitive function in adult animals. We have previously developed a mimetic peptide (FGL) from the neural cell adhesion molecule (NCAM) that enhances spatial learning and memory in rats. We have now investigated the cellular and molecular basis of this cognitive enhancement, using biochemical, morphological, electrophysiological, and behavioral analyses. We have found that FGL triggers a long-lasting enhancement of synaptic transmission in hippocampal CA1 neurons. This effect is mediated by a facilitated synaptic delivery of AMPA receptors, which is accompanied by enhanced NMDA receptor-dependent long-term potentiation (LTP). Both LTP and cognitive enhancement are mediated by an initial PKC activation, which is followed by persistent CaMKII activation. These results provide a mechanistic link between facilitation of AMPA receptor synaptic delivery and improved hippocampal-dependent learning, induced by a pharmacological cognitive enhancer.

摘要

细胞黏附分子及其下游的生长因子依赖信号通路对于脑发育和突触可塑性至关重要,并且与成年动物的认知功能相关联。我们先前从神经细胞黏附分子(NCAM)中开发出一种模拟肽(FGL),该肽可增强大鼠的空间学习和记忆。现在,我们使用生化、形态、电生理和行为分析方法研究了这种认知增强的细胞和分子基础。我们发现 FGL 可触发海马 CA1 神经元中突触传递的持久增强。这种作用是由 AMPA 受体的易化突触传递介导的,伴随着增强的 NMDA 受体依赖性长时程增强(LTP)。LTP 和认知增强均由初始蛋白激酶 C(PKC)激活介导,随后是持续的钙调蛋白依赖性激酶 II(CaMKII)激活。这些结果提供了一种机制联系,将 AMPA 受体突触传递的易化与药物认知增强剂诱导的海马依赖性学习的改善联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1058/3283560/9c2a7d0dbfed/pbio.1001262.g001.jpg

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