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海马苔藓纤维突触上突触前红藻氨酸受体的突触激活。

Synaptic activation of presynaptic kainate receptors on hippocampal mossy fiber synapses.

作者信息

Schmitz D, Frerking M, Nicoll R A

机构信息

Department of Cellular and Molecular Pharmacology, University of California, San Francisco 94143, USA.

出版信息

Neuron. 2000 Aug;27(2):327-38. doi: 10.1016/s0896-6273(00)00040-4.

Abstract

Kainate receptors (KARs) are a poorly understood family of ionotropic glutamate receptors. A role for these receptors in the presynaptic control of transmitter release has been proposed but remains controversial. Here, KAR agonists are shown to enhance fiber excitability, and a number of experiments show that this is a direct effect of KARs on the presynaptic fibers. In addition, KAR activation inhibits evoked transmitter release from mossy fiber synapses. Synaptic release of glutamate from either neighboring mossy fiber synapses or associational/commisural (A/C) synapses results in the activation of these presynaptic ionotropic KARs. These results, along with previous studies, indicate that KARs, through the endogenous release of glutamate, mediate excitatory postsynaptic potentials (EPSPs), alter presynaptic excitability, and modulate transmitter release.

摘要

红藻氨酸受体(KARs)是一类了解较少的离子型谷氨酸受体家族。这些受体在突触前对递质释放的控制中所起的作用已被提出,但仍存在争议。在这里,红藻氨酸受体激动剂被证明可增强纤维兴奋性,并且多项实验表明这是红藻氨酸受体对突触前纤维的直接作用。此外,红藻氨酸受体的激活会抑制苔藓纤维突触诱发的递质释放。来自相邻苔藓纤维突触或联合/连合(A/C)突触的谷氨酸的突触释放会导致这些突触前离子型红藻氨酸受体的激活。这些结果与先前的研究表明,红藻氨酸受体通过谷氨酸的内源性释放,介导兴奋性突触后电位(EPSPs),改变突触前兴奋性,并调节递质释放。

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