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Blockade by amino acid antagonists of neuronal excitation mediated by the pyramidal tract.

机译:被锥体束介导的神经元兴奋的氨基酸拮抗剂阻断。

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摘要

1.The responses to glutamate and amino acid antagonists of cells in the cuneate nucleus of anaesthetized rats have been examined.2. 1-hydroxy-3-amino-pyrrolidone-2 (HA-966) and glutamic acid diethylester applied by micro-iontophoresis reduced glutamate excitation of the neurons. HA-966 WAS EFFECTIVE ON MORE CELLS THAN GLUTAMIC ACID DIETHYLESTER AND WAS MORE POTENT. HA-966 DID NOT AFFECT EXCITATORY RESPONSES TO ACETYLCHOLINE.3. Spike activity of cuneate cells was evoked by stimulating the cerebral cortex. Spikeswhich could be attributed to monosynaptic activation of the cells were studied. The pyramidal tract is the only corticofugal pathway known to be capable of short latency activation of dorsal column nucleus neurones.4. HA-966 reversibly blocked the evoked activity in twenty-eight (70%) of forty units in which monosynaptically evoked spikes were induced.5. The results raise the possibility that the neurotransmitter released by neurones of the pyramidal tract may be an excitatory amino acid.
机译:1,研究了麻醉大鼠楔形核对细胞谷氨酸和氨基酸拮抗剂的反应; 2。通过微离子电渗疗法应用1-羟基-3-氨基-吡咯烷酮2(HA-966)和谷氨酸二乙酯可减少神经元的谷氨酸激发。 HA-966比谷氨酸二酯更有效地作用于细胞,而且潜力更大。 HA-966对乙酰胆碱没有兴奋性反应3。通过刺激大脑皮层诱发楔形细胞的刺突活性。研究了可能归因于细胞单突触激活的突触。锥体束是唯一已知的能够短暂延迟激活背柱核神经元的皮质性途径。4。 HA-966可逆地阻断了诱发单突触诱发峰值的40个单元中的28个(70%)诱发的活动。5。结果增加了锥体束神经元释放的神经递质可能是兴奋性氨基酸的可能性。

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