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海马突触可塑性中AMPA谷氨酸受体的基因操作。

Genetic manipulations of AMPA glutamate receptors in hippocampal synaptic plasticity.

作者信息

Gugustea Radu, Jia Zhengping

机构信息

The Hospital for Sick Children, Neurosciences and Mental Health Program, Peter Gilgan Centre for Research and Learning, Toronto, ON, Canada; Department of Physiology, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

The Hospital for Sick Children, Neurosciences and Mental Health Program, Peter Gilgan Centre for Research and Learning, Toronto, ON, Canada; Department of Physiology, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

出版信息

Neuropharmacology. 2021 Aug 15;194:108630. doi: 10.1016/j.neuropharm.2021.108630. Epub 2021 Jun 2.

Abstract

Alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) are the principal mediators of fast excitatory synaptic transmission and they are required for various forms of synaptic plasticity, including long-term potentiation (LTP) and depression (LTD), which are key mechanisms of learning and memory. AMPARs are tetrameric complexes assembled from four subunits (GluA1-4), however, the lack of subunit-specific pharmacological tools has made the assessment of individual subunits difficult. The application of genetic techniques, particularly gene targeting, allows for precise manipulation and dissection of each subunit in the regulation of neuronal function and behaviour. In this review, we summarize studies using various mouse models with genetically altered AMPARs and focus on their roles in basal synaptic transmission, LTP, and LTD at the hippocampal CA1 synapse. These studies provide strong evidence that there are multiple forms of LTP and LTD at this synapse which can be induced by various induction protocols, and they are differentially regulated by different AMPAR subunits and domains. We conclude that it is necessary to delineate the mechanism of each of these forms of plasticity and their contribution to memory and brain disorders.

摘要

α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPARs)是快速兴奋性突触传递的主要介质,它们参与多种形式的突触可塑性,包括长时程增强(LTP)和长时程抑制(LTD),而这两种形式是学习和记忆的关键机制。AMPARs是由四个亚基(GluA1 - 4)组装而成的四聚体复合物,然而,缺乏亚基特异性的药理学工具使得对单个亚基的评估变得困难。遗传技术的应用,特别是基因靶向技术,能够在调节神经元功能和行为方面对每个亚基进行精确的操作和剖析。在这篇综述中,我们总结了使用各种具有基因改变的AMPARs的小鼠模型进行的研究,并重点关注它们在海马CA1突触的基础突触传递、LTP和LTD中的作用。这些研究提供了强有力的证据,表明在这个突触处存在多种形式的LTP和LTD,它们可以由各种诱导方案诱导产生,并且受到不同AMPAR亚基和结构域的差异调节。我们得出结论,有必要阐明这些可塑性形式中的每一种的机制及其对记忆和脑部疾病的贡献。

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