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海马体中NMDA受体的频率依赖性参与:一种新型突触机制。

Frequency-dependent involvement of NMDA receptors in the hippocampus: a novel synaptic mechanism.

作者信息

Herron C E, Lester R A, Coan E J, Collingridge G L

出版信息

Nature. 1986;322(6076):265-8. doi: 10.1038/322265a0.

Abstract

Acidic amino acids, such as l-glutamate, are believed to be excitatory neurotransmitters in the mammalian brain and exert effects on several different receptors named after the selective agonists kainate, quisqualate and N-methyl-D-aspartate (NMDA). The first two receptors collectively termed non-NMDA receptors, have been implicated in the mediation of synaptic transmission in many excitatory pathways in the central nervous system (CNS), whereas NMDA receptors, with few exceptions do not appear to be involved; this is typified in the hippocampus where there is a high density of NMDA receptors yet selective NMDA receptor antagonists, such as D-2-amino-5-phosphonovalerate (APV), do not affect synaptic potentials. NMDA receptors have, however, been shown to be involved in long-term potentiation (LTP) in the hippocampus, a form of synaptic plasticity which may be involved in learning and memory. NMDA receptors have also been found to contribute to epileptiform activity in this region. We now describe how NMDA receptors can participate during high-frequency synaptic transmission in the hippocampus, their involvement during low-frequency transmission being greatly suppressed by Mg2+. A frequency dependent alleviation of this blockade provides a novel synaptic mechanism whereby a single neurotransmitter can transmit very different information depending on the temporal nature of the input. This mechanism could account for the involvement of NMDA receptors in the initiation of LPT and their contribution, in part, to epileptic activity.

摘要

酸性氨基酸,如L-谷氨酸,被认为是哺乳动物大脑中的兴奋性神经递质,并对几种以选择性激动剂海人酸、quisqualate和N-甲基-D-天冬氨酸(NMDA)命名的不同受体发挥作用。前两种受体统称为非NMDA受体,已被认为在中枢神经系统(CNS)许多兴奋性通路的突触传递介导中起作用,而NMDA受体,除少数例外,似乎不参与其中;这在海马体中表现得很典型,海马体中NMDA受体密度很高,但选择性NMDA受体拮抗剂,如D-2-氨基-5-磷酸戊酸(APV),并不影响突触电位。然而,已证明NMDA受体参与海马体中的长时程增强(LTP),这是一种可能与学习和记忆有关的突触可塑性形式。还发现NMDA受体在该区域的癫痫样活动中起作用。我们现在描述NMDA受体如何在海马体的高频突触传递过程中发挥作用,它们在低频传递过程中的作用被Mg2+大大抑制。这种阻断的频率依赖性缓解提供了一种新的突触机制,即单一神经递质可以根据输入的时间性质传递非常不同的信息。这种机制可以解释NMDA受体在LPT起始中的作用及其对癫痫活动的部分贡献。

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