维拉帕米减轻喹啉酸诱导的大鼠海马神经元损伤。

Neuropatologia polska Pub Date : 1993-01-01
E Matyja, E Kida
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引用次数: 0

摘要

研究了有机钙通道阻滞剂维拉帕米对大鼠海马培养喹啉酸(QUIN)神经毒性的影响。维拉帕米和奎因浓度均为100微米,同时加入培养基。超微结构分析显示维拉帕米能够减轻典型的奎恩诱导的组织损伤。特别是,暴露于两种药物后3和7天,大多数神经元和突触后树突的形态特征显示正常。这些结果支持了钙进入在QUIN神经毒性发展中的重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Verapamil reduces quinolinic acid-induced neuronal damage in rat hippocampus in vitro.

The effect of the organic calcium channel blocker, verapamil, on quinolinic acid (QUIN) neurotoxicity in rat hippocampal cultures was studied. Verapamil and QUIN, both in 100 microns concentration, were added simultaneously to the culture medium. Ultrastructural analysis showed that verapamil was able to reduce typical QUIN-induced tissue damages. Especially, 3 and 7 days after exposure to the two agents, majority of both neurons and postsynaptic dendrites revealed normally appearing morphological features. The results support the suggestion of the important role of calcium entry in the development of QUIN neurotoxicity.

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