Suppr超能文献

大鼠丘脑底核神经元皮质诱导兴奋的药理学研究:氨基酸作为假定神经递质的证据

Pharmacological study of the cortical-induced excitation of subthalamic nucleus neurons in the rat: evidence for amino acids as putative neurotransmitters.

作者信息

Rouzaire-Dubois B, Scarnati E

出版信息

Neuroscience. 1987 May;21(2):429-40. doi: 10.1016/0306-4522(87)90133-3.

Abstract

Extracellular records were made from subthalamic nucleus neurons during microiontophoretic application of drugs and stimulation of the corticosubthalamic nucleus pathway. In 87% of the subthalamic nucleus cells, cortical stimulation induced a powerful excitation, consisting of a burst of 1-7 spikes. This projection must arise from a large area of the cortex since stimulation of nearly all the ipsilateral cortex and the rostral two-thirds of the contralateral cortex was found to influence the activity of subthalamic nucleus neurons. Experiments were undertaken in order to determine the identity of the neurotransmitter involved in the corticosubthalamic nucleus pathway. Glutamic acid diethyl ester reversibly suppressed subthalamic nucleus excitations induced by ipsi- or contralateral cortical stimulation or microiontophoretically applied glutamate. On the same cells, this compound had no effect on acetylcholine-evoked excitation and gamma-aminobutyric acid-evoked inhibition and subthalamic excitation induced by stimulation of the tegmenti pedunculopontine nucleus. Atropine at doses which antagonized the acetylcholine response, flupenthixol at dose which antagonized the dopamine response, and bicuculline at doses which antagonized the gamma-aminobutyric acid response failed to block excitations evoked by cortical stimulation and by glutamate. These experiments excluded a role for acetylcholine, dopamine and gamma-aminobutyric acid in the cortically evoked excitation of subthalamic nucleus cells. Since an amino acid seemed to play a role as neurotransmitter of the corticosubthalamic nucleus pathway, further experiments were designed to confirm these data and to determine the contribution of each amino acid receptor type in the cortical-induced excitation of subthalamic cells. All the subthalamic cells recorded were also excited by microiontophoretically applied N-methyl-D-aspartic, quisqualic and kainic acids. The cortical-evoked activation of subthalamic nucleus neurons was reversibly suppressed by kynurenic acid and cis-2,3-piperidine dicarboxylic acid, two broad-spectrum antagonists of excitatory amino acids, microiontophoretically applied at doses which also blocked excitations induced by N-methyl-D-aspartic, quisqualic and kainic acids. Application of 2-amino-5-phosphonovaleric acid inhibited excitation induced by N-methyl-D-aspartic acid but not those elicited by quisqualic or kainic acid, while glutamate excitation was only slightly affected. This compound had no effect on the cortically evoked excitation of subthalamic nucleus neurons.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在药物微量离子导入应用以及刺激皮质 - 丘脑底核通路的过程中,从丘脑底核神经元进行细胞外记录。在87%的丘脑底核细胞中,皮质刺激诱发了强烈的兴奋,表现为一串1 - 7个峰电位。这种投射必定起源于皮质的大片区域,因为发现几乎所有同侧皮质以及对侧皮质前三分之二的刺激都会影响丘脑底核神经元的活动。进行这些实验是为了确定参与皮质 - 丘脑底核通路的神经递质的身份。谷氨酸二乙酯可逆性地抑制由同侧或对侧皮质刺激或微量离子导入应用谷氨酸所诱发的丘脑底核兴奋。在相同的细胞上,该化合物对乙酰胆碱诱发的兴奋、γ - 氨基丁酸诱发的抑制以及刺激被盖脚桥核所诱发的丘脑底核兴奋均无影响。能拮抗乙酰胆碱反应剂量的阿托品、能拮抗多巴胺反应剂量的氟哌噻吨以及能拮抗γ - 氨基丁酸反应剂量的荷包牡丹碱,均未能阻断由皮质刺激和谷氨酸所诱发的兴奋。这些实验排除了乙酰胆碱、多巴胺和γ - 氨基丁酸在皮质诱发的丘脑底核细胞兴奋中所起的作用。由于一种氨基酸似乎在皮质 - 丘脑底核通路中作为神经递质发挥作用,因此设计了进一步的实验来证实这些数据,并确定每种氨基酸受体类型在皮质诱发的丘脑底核细胞兴奋中的作用。所有记录的丘脑底核细胞也会被微量离子导入应用的N - 甲基 - D - 天冬氨酸、quisqualic酸和海人酸所兴奋。丘脑底核神经元的皮质诱发激活被犬尿氨酸和顺式 - 2,3 - 哌啶二羧酸可逆性抑制,这两种兴奋性氨基酸的广谱拮抗剂以能阻断由N - 甲基 - D - 天冬氨酸、quisqualic酸和海人酸所诱发兴奋的剂量进行微量离子导入应用。2 - 氨基 - 5 - 膦酰基戊酸的应用抑制了由N - 甲基 - D - 天冬氨酸诱发的兴奋,但对quisqualic酸或海人酸诱发的兴奋无抑制作用,而谷氨酸诱发的兴奋仅受到轻微影响。该化合物对皮质诱发的丘脑底核神经元兴奋无影响。(摘要截选至400字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验