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大脑中兴奋性突触处的谷氨酸受体可塑性。

Glutamate receptor plasticity at excitatory synapses in the brain.

作者信息

Genoux David, Montgomery Johanna M

机构信息

Department of Physiology, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.

出版信息

Clin Exp Pharmacol Physiol. 2007 Oct;34(10):1058-63. doi: 10.1111/j.1440-1681.2007.04722.x.

Abstract
  1. Synapse plasticity, defined as an activity dependent change in the strength of synapses, was first described in 1973 and, since those seminal experiments were reported, the field of synapse plasticity has expanded into one of the most widely studied areas in neuroscience. 2. Significant effort has been focused on determining the expression mechanisms of the changes in synapse strength. The present review will focus on the changes in the post-synaptic expression of glutamate receptors that have been shown to occur during the expression of synapse plasticity. 3. Biochemical studies of excitatory synapses in the central nervous system have revealed a high density of proteins concentrated at dendritic spines. These proteins appear to play critical roles in synaptic structure, plasticity and in trafficking receptors to synapses. 4. There is growing evidence that synapse plasticity could be the cellular basis of certain forms of learning and memory. Determining the behavioural correlates of this fundamental synaptic process will continue to be addressed in current and future research.
摘要
  1. 突触可塑性被定义为突触强度的活动依赖性变化,它于1973年首次被描述。自从这些开创性的实验被报道以来,突触可塑性领域已扩展成为神经科学中研究最广泛的领域之一。2. 大量的努力集中在确定突触强度变化的表达机制上。本综述将聚焦于谷氨酸受体突触后表达的变化,这些变化已被证明在突触可塑性表达过程中会发生。3. 对中枢神经系统兴奋性突触的生化研究表明,树突棘处集中了高密度的蛋白质。这些蛋白质似乎在突触结构、可塑性以及将受体运输到突触中发挥着关键作用。4. 越来越多的证据表明,突触可塑性可能是某些形式学习和记忆的细胞基础。确定这一基本突触过程与行为的相关性将在当前和未来的研究中继续得到探讨。

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