Renard A, Crepel F
Laboratoire de Neurobiologie et Neuropharmacologie du Développment, CNRS ERS 100, Bâtiment 441, Université Paris-Sud, 91405 Orsay Cedex, France.
Eur J Neurosci. 1996 May;8(5):978-87. doi: 10.1111/j.1460-9568.1996.tb01585.x.
The effects of glutamate, aspartate and N-methyl-D-aspartate (NMDA) on Purkinje cells and interneurons were investigated in cerebellar slice cultures using the whole-cell configuration of the patch-clamp technique. L-Glutamate and L-aspartate induced inward currents in Purkinje cells voltage-clamped at -60 mV. In standard external solution, the amplitude of the responses induced by the two amino-acids was a linear function of the membrane potential. L-Aspartate-induced currents were inhibited by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), a selective antagonist of non-NMDA receptors. NMDA, a selective agonist of NMDA receptors, had no effect of its own on the excitability of Purkinje cells, but was effective in blocking the responses induced by aspartate in Purkinje cells in a voltage-independent manner. In contrast, D-(-)-2-amino-5-phosphonovaleric acid (D-APV), a selective antagonist of NMDA receptors, had no effect on aspartate-induced responses. D-Aspartate also induced responses in Purkinje cells, and the amplitude of these responses was a linear function of the membrane potential. Currents induced by L- and D-aspartate were inhibited by dihydrokainate, a glutamate uptake blocker. In sodium-free external solution, glutamate still induced outward currents in Purkinje cells, whereas L- and D-aspartate no longer evoked any current. When sodium was replaced by lithium in the external medium, no change in the holding current could be detected in Purkinje cells maintained at -60 mV; moreover, in this bathing medium L-aspartate no longer evoked any current whereas glutamate-induced responses were still present. In contrast, interneurons were sensitive to both NMDA and aspartate applications, and these responses were antagonized by D-APV. In addition, aspartate still induced an outward current in sodium-free external solution. This study presents rather direct evidence in favour of L-aspartate as being a very selective NMDA receptor agonist in the cerebellum. L-Aspartate-induced currents in Purkinje cells are not due to activation of mixed NMDA/non-NMDA receptors, but are probably due to the release of L-glutamate induced by aspartate through glutamate uptake.
利用膜片钳技术的全细胞记录模式,在小脑薄片培养物中研究了谷氨酸、天冬氨酸和N-甲基-D-天冬氨酸(NMDA)对浦肯野细胞和中间神经元的作用。L-谷氨酸和L-天冬氨酸可在钳制于-60mV的浦肯野细胞中诱导内向电流。在标准细胞外溶液中,这两种氨基酸所诱导反应的幅度是膜电位的线性函数。L-天冬氨酸诱导的电流可被6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)抑制,CNQX是非NMDA受体的选择性拮抗剂。NMDA是NMDA受体的选择性激动剂,其本身对浦肯野细胞的兴奋性无影响,但能以电压非依赖性方式有效阻断天冬氨酸在浦肯野细胞中诱导的反应。相反,NMDA受体的选择性拮抗剂D-(-)-2-氨基-5-磷酸戊酸(D-APV)对天冬氨酸诱导的反应无影响。D-天冬氨酸也能在浦肯野细胞中诱导反应,且这些反应的幅度是膜电位的线性函数。L-和D-天冬氨酸诱导的电流可被谷氨酸摄取阻断剂二氢海人藻酸抑制。在无钠的细胞外溶液中,谷氨酸仍可在浦肯野细胞中诱导外向电流,而L-和D-天冬氨酸不再诱发任何电流。当细胞外培养基中的钠被锂取代时,在钳制于-60mV的浦肯野细胞中未检测到静息电流的变化;此外,在此浴液中,L-天冬氨酸不再诱发任何电流,而谷氨酸诱导的反应仍然存在。相反,中间神经元对NMDA和天冬氨酸的应用均敏感,且这些反应可被D-APV拮抗。此外,在无钠的细胞外溶液中,天冬氨酸仍可诱导外向电流。本研究提供了相当直接的证据,支持L-天冬氨酸是小脑中一种非常选择性的NMDA受体激动剂。L-天冬氨酸在浦肯野细胞中诱导的电流并非由于混合的NMDA/非NMDA受体的激活,而可能是由于天冬氨酸通过谷氨酸摄取诱导L-谷氨酸的释放所致。