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蛋白水解酶不会破坏新生大鼠急性分离海马CA1和CA3神经元的N-甲基-D-天冬氨酸(NMDA)敏感性。

Proteolytic enzymes do not destroy the N-methyl-D-aspartate (NMDA) sensitivity of acutely isolated hippocampal CA1 and CA3 neurons from postnatal rats.

作者信息

Gündel J, Steinhäuser C, Matthies H

机构信息

Institute for Neurobiology and Brain Research, Academy of Sciences GDR, Magdeburg.

出版信息

Neurosci Lett. 1990 Nov 13;119(2):249-52. doi: 10.1016/0304-3940(90)90845-z.

DOI:10.1016/0304-3940(90)90845-z
PMID:1704112
Abstract

Using whole cell recordings in combination with the concentration clamp technique it was shown that even enzymatically isolated hippocampal CA1 and CA3 neurons exhibit N-methyl-D-aspartate (NMDA) and L-aspartate currents. These currents were completely blocked by 0.5 mM Mg2+ or partially blocked (72.7 +/- 2.4%) by DL-2-amino-5-phosphonovalerate (50 microM) whereas 10 microM glycine (Gly) potentiated the NMDA responses (3.1 +/- 1.6-fold). A half-maximum dose of 55 microM was calculated from the sigmoid NMDA dose-response curve in the presence of 10 microM Gly. The amplitudes of these currents did not depend on the type of the proteolytic enzyme used for cell isolation.

摘要

运用全细胞记录技术结合浓度钳制技术表明,即使是经酶解分离的海马CA1和CA3神经元也表现出N-甲基-D-天冬氨酸(NMDA)电流和L-天冬氨酸电流。这些电流可被0.5 mM Mg2+完全阻断,或被DL-2-氨基-5-磷酸戊酸(50 microM)部分阻断(72.7±2.4%),而10 microM甘氨酸(Gly)可增强NMDA反应(3.1±1.6倍)。根据在10 microM Gly存在下的S形NMDA剂量反应曲线计算出半数最大剂量为55 microM。这些电流的幅度并不取决于用于细胞分离的蛋白水解酶的类型。

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