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兴奋性氨基酸对培养的鸡脊髓神经元的作用。

The action of excitatory amino acids on chick spinal cord neurones in culture.

作者信息

Vlachová V, Vyklický L, Vyklický L, Vyskocil F

机构信息

Institute of Physiology, Czechoslovak Academy of Sciences, Prague.

出版信息

J Physiol. 1987 May;386:425-38. doi: 10.1113/jphysiol.1987.sp016542.

DOI:10.1113/jphysiol.1987.sp016542
PMID:2445965
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1192470/
Abstract
  1. Membrane currents evoked by N-methyl-D-aspartate (NMDA), L-aspartate, L-glutamate, quisqualate and kainate were studied in cultured neurones from the embryonic chick spinal cord by the patch-clamp technique and by employing a quasi-step microperfusion technique. 2. Application of NMDA, aspartate, glutamate and quisqualate induced currents which exhibited an initial peak which declined to a plateau level with a time constant of 2 s and then remained constant or slowly decreased. The discontinuation of the application was followed by an after-current. The individual components of the responses were insensitive to TTX (2 X 10(-6) M) and were present in neurones which did not exhibit any sign of synaptic activity. The responses induced by kainate were monophasic and declined slowly during long-lasting application. 3. The responses induced by NMDA, aspartate and glutamate were voltage dependent, while those induced by kainate were linear between -80 and +80 mV. The equilibrium potential for all components of the responses to all excitatory amino acids was close to zero. 4. From dose-response curves the half-maximum effective dose (ED50) for glutamate and kainate was 3 X 10(-5) and 2 X 10(-4) M respectively. The Hill coefficients for the glutamate and the kainate were calculated to be 1.8 +/- 0.1 (n = 4) and 1.9 +/- 0.5 (n = 4) respectively. Thus two molecules may be interacting with each of the receptor-activated ion channels. 5. Interaction between kainate and quisqualate or kainate and NMDA was studied at both negative and positive holding potentials. No summation of the responses was found when kainate at concentrations close to those required for evoking the maximum response was applied simultaneously with quisqualate or NMDA. On the contrary, a diminution of the membrane currents was observed. A marked decrease in membrane currents was also observed when glutamate (10(-4) M) was applied simultaneously with aspartate (10(-4) M). 6. Glutamate-activated single-channel currents were recorded in the cell-attached configuration with electrodes filled with glutamate (20 microM) in five neurones and a conductance approximately 50 pS was found. 7. It is suggested that differences in the potency of the different excitatory amino acids as open-channel blockers may be one of the mechanisms which contribute to the diversity in the action of excitatory amino acids and that at least some of the effects of NMDA, aspartate, glutamate, quisqualate and kainate may be mediated by a common receptor-channel complex.
摘要
  1. 运用膜片钳技术并采用准阶跃微量灌注技术,对来自胚胎鸡脊髓的培养神经元中由N-甲基-D-天冬氨酸(NMDA)、L-天冬氨酸、L-谷氨酸、quisqualate和海人藻酸诱发的膜电流进行了研究。2. 施加NMDA、天冬氨酸、谷氨酸和quisqualate会诱发出电流,这些电流呈现出一个初始峰值,该峰值以2秒的时间常数下降至平台期水平,然后保持恒定或缓慢下降。停止施加后会出现尾电流。这些反应的各个成分对TTX(2×10⁻⁶ M)不敏感,并且存在于未表现出任何突触活动迹象的神经元中。海人藻酸诱发的反应是单相的,在长时间施加过程中缓慢下降。3. NMDA、天冬氨酸和谷氨酸诱发的反应是电压依赖性的,而海人藻酸诱发的反应在-80至+80 mV之间呈线性。对所有兴奋性氨基酸反应的所有成分的平衡电位都接近零。4. 根据剂量-反应曲线,谷氨酸和海人藻酸的半数有效剂量(ED50)分别为3×10⁻⁵ M和2×10⁻⁴ M。谷氨酸和海人藻酸的希尔系数经计算分别为1.8±0.1(n = 4)和1.9±0.5(n = 4)。因此,可能有两个分子与每个受体激活的离子通道相互作用。5. 在负和正的钳制电位下研究了海人藻酸与quisqualate或海人藻酸与NMDA之间的相互作用。当以接近诱发最大反应所需浓度的海人藻酸与quisqualate或NMDA同时施加时,未发现反应的总和。相反,观察到膜电流减小。当谷氨酸(10⁻⁴ M)与天冬氨酸(10⁻⁴ M)同时施加时,也观察到膜电流明显下降。6. 在五个神经元中,用填充有谷氨酸(20 μM)的电极在细胞贴附模式下记录了谷氨酸激活的单通道电流,发现电导约为50 pS。7. 有人提出,不同兴奋性氨基酸作为开放通道阻滞剂的效力差异可能是导致兴奋性氨基酸作用多样性的机制之一,并且NMDA、天冬氨酸、谷氨酸、quisqualate和海人藻酸的至少一些作用可能由共同的受体-通道复合物介导。

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Selective antagonism of amino acid-induced and synaptic excitation in the cat spinal cord.猫脊髓中氨基酸诱导的和突触兴奋的选择性拮抗作用。
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