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生理证据表明,D-天冬氨酸激活了一种不同于加利福尼亚海兔神经元中离子型谷氨酸受体电流的电流。

Physiological evidence that D-aspartate activates a current distinct from ionotropic glutamate receptor currents in Aplysia californica neurons.

机构信息

Division of Marine Biology and Fisheries, Rosenstiel School of Marine and Atmospheric Science, University of Miami, Miami, Florida, USA.

出版信息

J Neurophysiol. 2011 Oct;106(4):1629-36. doi: 10.1152/jn.00403.2011. Epub 2011 Jul 13.

DOI:10.1152/jn.00403.2011
PMID:21753031
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3191832/
Abstract

D-Aspartate (D-Asp) activates an excitatory current in neurons of Aplysia californica. Although D-Asp is presumed to activate a subset of L-glutamate (L-Glu) channels, the identities of putative d-Asp receptors and channels are unclear. Whole cell voltage- and current-clamp studies using primary cultures of Aplysia buccal S cluster (BSC) neurons were executed to characterize D-Asp-activated ion channels. Both D-Asp and L-Glu evoked currents with similar current-voltage relationships, amplitudes, and relatively slow time courses of activation and inactivation when agonists were pressure applied. D-Asp-induced currents, however, were faster and desensitized longer, requiring 40 s to return to full amplitude. Of cells exposed to both agonists, 25% had D-Asp- but not L-Glu-induced currents, suggesting a receptor for D-Asp that was independent of l-Glu receptors. D-Asp channels were permeable to Na(+) and K(+), but not Ca²⁺, and were vulnerable to voltage-dependent Mg²⁺ block similarly to vertebrate NMDA receptor (NMDAR) channels. d-Asp may activate both NMDARs and non-l-Glu receptors in the nervous system of Aplysia.

摘要

天冬氨酸(D-Asp)在加利福尼亚海兔的神经元中激活兴奋性电流。虽然 D-Asp 被认为可以激活一组 L-谷氨酸(L-Glu)通道,但假定的 D-Asp 受体和通道的身份尚不清楚。使用加利福尼亚海兔口腔 S 簇(BSC)神经元的原代培养物进行全细胞膜电压和电流钳研究,以表征 D-Asp 激活的离子通道。当激动剂加压时,D-Asp 和 L-Glu 均能引起具有相似电流-电压关系、幅度和相对较慢激活和失活时间过程的电流。然而,D-Asp 诱导的电流更快,脱敏时间更长,需要 40 秒才能恢复到全幅度。在暴露于两种激动剂的细胞中,有 25%的细胞具有 D-Asp 但没有 L-Glu 诱导的电流,这表明存在一种独立于 l-Glu 受体的 D-Asp 受体。D-Asp 通道对 Na(+)和 K(+)具有通透性,但对 Ca²⁺没有通透性,并且对电压依赖性 Mg²⁺阻断的敏感性类似于脊椎动物 NMDA 受体(NMDAR)通道。D-Asp 可能在加利福尼亚海兔的神经系统中激活 NMDAR 和非 l-Glu 受体。

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本文引用的文献

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Unique ionotropic receptors for D-aspartate are a target for serotonin-induced synaptic plasticity in Aplysia californica.独特的 D-天冬氨酸离子型受体是 Aplysia californica 中 5-羟色胺诱导的突触可塑性的靶点。
Comp Biochem Physiol C Toxicol Pharmacol. 2012 Jan;155(1):151-9. doi: 10.1016/j.cbpc.2011.04.001. Epub 2011 Apr 9.
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Molecular basis of NMDA receptor functional diversity.NMDA 受体功能多样性的分子基础。
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A novel pyridoxal 5'-phosphate-dependent amino acid racemase in the Aplysia californica central nervous system.在加利福尼亚海兔中枢神经系统中存在一种新型的依赖吡哆醛 5'-磷酸的氨基酸消旋酶。
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Changes in D-aspartate ion currents in the Aplysia nervous system with aging.衰老过程中,海兔神经系统中 D-天冬氨酸离子流的变化。
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Increased levels of d-aspartate in the hippocampus enhance LTP but do not facilitate cognitive flexibility.海马体中D-天冬氨酸水平的升高会增强长时程增强效应,但不会促进认知灵活性。
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Modulation of an AMPA-like glutamate receptor (SqGluR) gating by L- and D-aspartic acids.L-天冬氨酸和D-天冬氨酸对一种AMPA样谷氨酸受体(SqGluR)门控的调节作用。
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