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豚鼠孤束核内侧神经元的兴奋性氨基酸受体

Excitatory amino acid receptors of guinea pig medial nucleus tractus solitarius neurons.

作者信息

Drewe J A, Miles R, Kunze D L

机构信息

Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston 77030.

出版信息

Am J Physiol. 1990 Nov;259(5 Pt 2):H1389-95. doi: 10.1152/ajpheart.1990.259.5.H1389.

Abstract

Neurons isolated from the medial subnuclei of nucleus tractus solitarius in adult guinea pigs were studied for responses to the excitatory amino acid glutamate and its analogues using the whole cell tight-seal voltage clamp technique. In 80% of the cells studied (n = 60) 100 microM glutamate produced inward currents at negative voltages. To further characterize the glutamate response, the agonists for three glutamate receptor subtypes, N-methyl-D-aspartate (NMDA), kainate, and quisqualate, were examined for their effects on membrane conductance. NMDA (25-250 microM) activated currents in 85% of the neurons tested (n = 30). NMDA currents were generally very small in amplitude. Of the neurons tested, 84% responded to kainate (10-30 microM, n = 19) and only 50% to quisqualate (25-50 microM, n = 26). The conductance activated by NMDA was outwardly rectifying. The conductance activated by kainate was voltage independent, while that activated by quisqualate showed varying degrees of outward rectification. Responses to NMDA were specifically antagonized by DL-2-amino-5-phosphonovaleric acid (AP-5, 50-100 microM). Kainate responses were blocked by kynurenate at concentrations (0.5-1.5 mM) ineffective on quisqualate-induced current. Glutamic acid diethyl ester (GDEE, 2-15 mM) was effective in reducing quisqualate responses at concentrations that had no effect on kainate responses. This characterization of the glutamate receptor subtypes and effective antagonists provides a basis for future determination of the specific receptor of glutamate responsible for mediation of the excitatory postsynaptic potentials produced by activation of the baroreceptor input.

摘要

利用全细胞膜片钳技术,研究了从成年豚鼠孤束核内侧亚核分离出的神经元对兴奋性氨基酸谷氨酸及其类似物的反应。在研究的80%的细胞(n = 60)中,100微摩尔谷氨酸在负电压下产生内向电流。为了进一步表征谷氨酸反应,检测了三种谷氨酸受体亚型的激动剂N-甲基-D-天冬氨酸(NMDA)、海人酸和quisqualate对膜电导的影响。NMDA(25 - 250微摩尔)在85%的测试神经元(n = 30)中激活电流。NMDA电流的幅度通常非常小。在测试的神经元中,84%对海人酸(10 - 30微摩尔,n = 19)有反应,而对quisqualate(25 - 50微摩尔,n = 26)有反应的仅为50%。由NMDA激活的电导呈外向整流。由海人酸激活的电导与电压无关,而由quisqualate激活的电导则表现出不同程度的外向整流。对NMDA的反应被DL - 2 - 氨基 - 5 - 磷酸戊酸(AP - 5,50 - 100微摩尔)特异性拮抗。海人酸反应被犬尿烯酸在对quisqualate诱导电流无效的浓度(0.5 - 1.5毫摩尔)下阻断。谷氨酸二乙酯(GDEE,2 - 15毫摩尔)在对海人酸反应无影响的浓度下有效降低quisqualate反应。谷氨酸受体亚型及其有效拮抗剂的这种表征为未来确定负责介导压力感受器输入激活产生的兴奋性突触后电位的谷氨酸特异性受体提供了基础。

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