1组代谢性谷氨酸受体激动剂引起大鼠海马神经变性。

Journal fur Hirnforschung Pub Date : 1997-01-01
W Y Ong, V J Balcar
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引用次数: 0

摘要

I组代谢性谷氨酸受体的激活导致胞浆内Ca2+的增加。细胞质中高水平的游离Ca2+可能对细胞有毒。我们现在报道,脑室内注射I组代谢性谷氨酸受体激动剂(S)-3,5-二羟基苯基甘氨酸(DHPG)可在数小时内改变海马中嗜离子性谷氨酸受体的分布,并延迟(4-7天)海马锥体神经元的损失。注射谷氨酸转运体底物没有导致神经元的损失,并且NMDA激动剂产生的病变与(S)-DHPG引起的病变不同。这些结果表明,体内I组代谢性谷氨酸受体的激活确实可能导致神经毒性事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Group I metabotropic glutamate receptor agonist causes neurodegeneration in rat hippocampus.

Activation of group I metabotropic glutamate receptors results in an increase in cytosolic Ca2+. High levels of free Ca2+ in the cytoplasm could be toxic to cells. We now report that intracerebroventricular injections of a group I metabotropic glutamate receptor agonist (S)-3,5-dihydroxyphenylglycine (DHPG) leads, within hours, to changes in the distribution of ionotropic glutamate receptors in the hippocampus and a delayed (4-7 days) loss of hippocampal pyramidal neurons. Injection of glutamate transporter substrates resulted in no loss of neurons and the administration of an NMDA agonist produced lesions different from those caused by (S)-DHPG. These results suggest that the activation of metabotropic glutamate receptors of group I in vivo may indeed result in neurotoxic events.

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