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Non-ionotropic cross-talk between AMPA and NMDA receptors in rodent hippocampal neurones

机译:啮齿类海马神经元中AMPA和NMDA受体之间的非离子串扰

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摘要

Many fast excitatory synapses in the hippocampus are enriched with both AMPARs (α-amino-3-hydroxyl-5-methyl-4-isoxazolepropionate receptors) and NMDARs (N-methyl-d-aspartate receptors). Their proximity allows them to be activated simultaneously by the same neurotransmitter, l-glutamate. Activation of AMPARs leads to influx of sodium and calcium ions, which can increase or decrease NMDAR activity through sodium concentration-dependent cascades or a calcium-calmodulin-dependent inactivation process, respectively. Here we provide evidence that the activation of AMPARs inhibits NMDARs through a non-ionotropic mechanism. NMDA-induced current in isolated rat CA1 hippocampal cells and nucleated patches of cultured mouse hippocampal neurones decreased when AMPARs were activated. Conversely, when AMPARs were blocked, the NMDA component of glutamate-induced current increased. The inhibitory action of AMPAR activation on NMDAR-mediated current depends upon the open state of AMPA channels and rapidly diminishes after deactivation of AMPARs. The inhibitory action was independent of membrane voltage, univalent cation fluxes and calcium influx. The AMPA-NMDA cross-inhibition also occurred in evoked synaptic current in CA1 neurones from intact mouse hippocampal slices. This cross-talk may play a role in preventing overexcitation during bursting activities in the hippocampus.
机译:海马中的许多快速兴奋性突触都富含AMPAR(α-氨基-3-羟基-5-甲基-4-异恶唑丙酸酯受体)和NMDAR(N-甲基-d-天冬氨酸受体)。它们的接近使得它们可以被相同的神经递质l-谷氨酸同时激活。 AMPAR的激活导致钠离子和钙离子的流入,这可以分别通过钠浓度依赖性级联反应或钙钙调蛋白依赖性灭活过程来增加或减少NMDAR活性。在这里,我们提供证据表明AMPAR的激活通过非离子型机制抑制NMDAR。激活AMPAR后,分离的大鼠CA1海马细胞中NMDA诱导的电流和培养的小鼠海马神经元的有核斑减少。相反,当AMPAR被阻断时,谷氨酸诱导电流的NMDA成分增加。 AMPAR激活对NMDAR介导的电流的抑制作用取决于AMPA通道的开放状态,并在AMPAR失活后迅速减少。抑制作用与膜电压,单价阳离子通量和钙流入无关。 AMPA-NMDA交叉抑制也发生在来自完整小鼠海马切片的CA1神经元引起的突触电流中。这种串扰可能在防止海马突发活动期间的过度兴奋中起作用。

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