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海马体长期增强效应以及学习与记忆中的代谢型谷氨酸受体

Metabotropic glutamate receptors in hippocampal long-term potentiation and learning and memory.

作者信息

Riedel G, Reymann K G

机构信息

Department of Neurophysiology, Federal Institute for Neurobiology, Magdeburg, Germany.

出版信息

Acta Physiol Scand. 1996 May;157(1):1-19. doi: 10.1046/j.1365-201X.1996.484231000.x.

Abstract

Glutamate receptors have been identified as important interfaces in learning and memory paradigms as well as in mechanisms of synaptic plasticity, such as long-term potentiation (LTP) and long-term depression (LTD), which are believed to be the underlying cellular basis of at least some forms of learning. Although investigations of G-protein-coupled receptors have a long history, those depending on ligand-binding of glutamate have only been discovered recently, and this is the reason why our knowledge about metabotropic glutamate receptors (mGluRs) is at present very limited. However, the development of relatively specific antagonists and agonists has enabled the analysis of the role of mGluRs in synaptic plasticity, mostly studied on the models of LTP and LTD. Among others, we have been able to demonstrate that activation of mGluRs is essential for induction and maintenance of long-lasting hippocampal LTP in vitro and in vivo. The work conducted by several groups, including ours, has now provided compelling evidence that mGluR activation is an important step in the cellular cascades leading to memory formation in vertebrates. This led us to assume, given that the hippocampus plays a prominent role in spatial rather than discrimination learning, that mGluRs may participate in the processing of spatial information via hippocampal mechanisms, and may thus be similarly important as N-methyl-D-aspartate receptors. This article surveys the literature dealing with mGluRs in hippocampal LTP and learning and memory. We will demonstrate that, although the understanding of cellular mechanisms of neuronal plasticity and of the pharmacology of learning and memory has advanced, the missing link to prove that LTP is a substrate for some form forms of learning still remains unsolved. Nevertheless, it appears reasonable to argue that mGluRs in LTP and learning may share some, but not all features, and it will be an interesting approach for further analysis to address the unresolved issues.

摘要

谷氨酸受体已被确认为学习和记忆范式以及突触可塑性机制(如长时程增强(LTP)和长时程抑制(LTD))中的重要界面,而LTP和LTD被认为是至少某些形式学习的潜在细胞基础。尽管对G蛋白偶联受体的研究历史悠久,但依赖谷氨酸配体结合的受体直到最近才被发现,这就是为什么我们目前对代谢型谷氨酸受体(mGluRs)的了解非常有限的原因。然而,相对特异性拮抗剂和激动剂的开发使得对mGluRs在突触可塑性中的作用进行分析成为可能,这主要是在LTP和LTD模型上进行研究的。其中,我们已经能够证明mGluRs的激活对于体外和体内持久海马LTP的诱导和维持至关重要。包括我们在内的几个研究小组所做的工作现在已经提供了令人信服的证据,表明mGluR激活是导致脊椎动物记忆形成的细胞级联反应中的重要一步。鉴于海马体在空间学习而非辨别学习中起突出作用,这使我们推测mGluRs可能通过海马机制参与空间信息的处理,因此可能与N-甲基-D-天冬氨酸受体同样重要。本文综述了有关海马LTP以及学习和记忆中mGluRs的文献。我们将证明,尽管对神经元可塑性的细胞机制以及学习和记忆药理学的理解已经取得进展,但证明LTP是某些形式学习的基础这一缺失环节仍然未得到解决。然而,有理由认为LTP和学习中的mGluRs可能有一些但并非所有共同特征,解决这些未解决的问题将是进一步分析的有趣方法。

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