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非N-甲基-D-天冬氨酸受体介导大鼠动眼神经副核突触处新小脑的兴奋。

Non-N-methyl-D-aspartate receptors mediate neocerebellar excitation at accessory oculomotor nuclei synapses of the rat.

作者信息

Bosco G, Casabona A, Perciavalle V

机构信息

Instituto di Fisiologia umana, Università di Catania, Italy.

出版信息

Arch Ital Biol. 1994 Oct;132(4):215-27.

PMID:7893196
Abstract

The nature of the receptor which mediates cerebellar-evoked monosynaptic excitations recorded from the accessory oculomotor nuclei (AON), i.e. the nucleus of posterior commissure, the nucleus of Darkschewitsch and the interstitial nucleus of Cajal, was studied in adult rats. Effects of exogenously applied excitatory amino acid (EAA) agonists N-methyl-D-aspartate (NMDA) and quisqualate (QUIS) and of selective NMDA receptor antagonist 2-amino-5-phosphonovaleric acid (2APV) and non-NMDA receptor antagonist 6,7-dinitroquinoxaline-2,3-dione (DNQX) were examined on both amino acid induced and synaptic excitation. Microiontophoretic application of NMDA and QUIS in the AON of the rat increases the neuronal discharge in a dose-dependent manner. These findings suggest that in the rat cells belonging to AON bear both NMDA and non-NMDA receptors. This result was confirmed by the fact that applications of 2APV selectively antagonized NMDA-induced responses without affecting those to QUIS, while DNQX blocked specifically the excitatory responses to QUIS and did not affect NMDA-mediated excitations. We did not observe any difference, between rats anesthetized with urethane and those anesthetized with halothane, with respect to capability of EAA agonists NMDA and QUIS to increase the AON cells activity and of EAA receptor antagonists 2APV and DNQX to abolish the NMDA-induced and the QUIS-induced effects, respectively. In addition, monosynaptic excitations induced by the stimulation of cerebellar lateral nucleus were abolished by microiontophoretic application of DNQX, but not of 2APV. This finding indicates that neocerebellar inputs activate specifically non-NMDA receptors of AON neurons.

摘要

在成年大鼠中研究了介导从辅助动眼神经核(AON)记录到的小脑诱发单突触兴奋的受体性质,AON即后连合核、达克谢维奇核和 Cajal 间质核。研究了外源性应用兴奋性氨基酸(EAA)激动剂 N-甲基-D-天冬氨酸(NMDA)和喹啉酸(QUIS)以及选择性 NMDA 受体拮抗剂 2-氨基-5-磷酸戊酸(2APV)和非 NMDA 受体拮抗剂 6,7-二硝基喹喔啉-2,3-二酮(DNQX)对氨基酸诱导的兴奋和突触兴奋的影响。在大鼠 AON 中微量离子导入 NMDA 和 QUIS 以剂量依赖方式增加神经元放电。这些发现表明,在大鼠中,属于 AON 的细胞同时具有 NMDA 和非 NMDA 受体。2APV 的应用选择性拮抗 NMDA 诱导的反应而不影响对 QUIS 的反应,而 DNQX 特异性阻断对 QUIS 的兴奋性反应且不影响 NMDA介导的兴奋,这一事实证实了该结果。在用乌拉坦麻醉的大鼠和用氟烷麻醉的大鼠之间,我们未观察到 EAA 激动剂 NMDA 和 QUIS 增加 AON 细胞活性以及 EAA 受体拮抗剂 2APV 和 DNQX 分别消除 NMDA 诱导和 QUIS 诱导效应的能力有任何差异。此外,微量离子导入 DNQX 可消除小脑外侧核刺激诱导的单突触兴奋,但 2APV 则不能。这一发现表明新小脑输入特异性激活 AON 神经元的非 NMDA受体。

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