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大鼠离体外侧臂旁核神经元中兴奋性氨基酸反应的电生理特性

Electrophysiological characterization of excitatory amino acid responses in rat lateral parabrachial neurons in vitro.

作者信息

Zidichouski J A, Jhamandas J H

机构信息

Department of Medicine (Neurology), University of Alberta, Edmonton, Canada.

出版信息

Brain Res. 1993 May 21;611(2):313-21. doi: 10.1016/0006-8993(93)90518-r.

Abstract

The pontine parabrachial nucleus (PBN) is a major recipient of a diverse array of autonomic-related information from the caudal brainstem. Recent data indicate the presence of glutamate-like immunoreactivity within this nucleus. The effect of specific excitatory amino acid (EAA) receptor agonists and antagonists were studied in the lateral PBN (LPBN) by the use of whole-cell patch recordings in an in vitro brainstem slice preparation. Under current and voltage clamp conditions, independent bath applications of N-methyl-D-aspartate (NMDA; 10 microM), quisqualic acid (QUIS; 10 microM) and kainic acid (kainate; 10 microM) evoked membrane depolarization and an inward current in 28 of 31 LPBN neurons. In voltage clamp mode, the NMDA current (INMDA) was undetectable at potentials negative to -70 mV and a small inward current was observed at more depolarized potentials. However, in the absence of external Mg2+, the voltage dependence of INMDA was similar to that observed for QUIS and kainate. The allosteric modulation of the NMDA receptor by the strychnine-insensitive glycine binding site was examined by the application of the amino acid D-serine (0.5 mM). A marked and sustained potentiation of the steady-state INMDA (-60 mV holding potential) was observed. The selective NMDA-antagonist DL-2-amino-5-phosphonovaleric acid (APV; 10 microM) completely and reversibly blocked the NMDA-induced current, that was maximized in the absence of external Mg2+. Furthermore, this dose of APV was found to reversibly reduce the firing frequency of spontaneously active LPBN neurons.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

脑桥臂旁核(PBN)是来自脑干尾部多种自主神经相关信息的主要接收部位。近期数据表明该核内存在谷氨酸样免疫反应性。利用体外脑干切片制备中的全细胞膜片钳记录技术,研究了特异性兴奋性氨基酸(EAA)受体激动剂和拮抗剂对外侧PBN(LPBN)的作用。在电流钳和电压钳条件下,分别浴用N - 甲基 - D - 天冬氨酸(NMDA;10微摩尔)、quisqualic酸(QUIS;10微摩尔)和海人酸(kainate;10微摩尔),在31个LPBN神经元中有28个诱发了膜去极化和内向电流。在电压钳模式下,在负于 - 70毫伏的电位时检测不到NMDA电流(INMDA),在更去极化的电位时观察到一个小的内向电流。然而,在无细胞外Mg2 +时,INMDA的电压依赖性与QUIS和海人酸的相似。通过应用氨基酸D - 丝氨酸(0.5毫摩尔)研究了士的宁不敏感甘氨酸结合位点对NMDA受体的变构调节。观察到稳态INMDA( - 60毫伏钳制电位)有显著且持续的增强。选择性NMDA拮抗剂DL - 2 - 氨基 - 5 - 磷酸戊酸(APV;10微摩尔)完全且可逆地阻断了NMDA诱导的电流,在无细胞外Mg2 +时该电流最大。此外,发现该剂量的APV可可逆地降低自发活动的LPBN神经元的放电频率。(摘要截短于250字)

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