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首页> 外文期刊>Neuroreport >Ca2+-dependent desensitization of AMPA receptors.
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Ca2+-dependent desensitization of AMPA receptors.

机译:Ca2 +依赖性的AMPA受体脱敏。

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The effect of changes in the external concentrations (0.4-10 mM) of Ca2+ ions on AMPA receptors (AMPARs) of different subunit composition was studied on freshly isolated rat brain neurones. Ca2+ produces rapid and reversible voltage-independent inhibition of AMPARs. Ca2+-permeable and Ca2+-impermeable AMPARs are equally sensitive to external Ca2+ suggesting that the effect is not addressed to the ion channel. The inhibition of responses evoked by AMPA is significantly larger than those evoked by kainate or glutamate. Cyclothiazide and aniracetam, which are known to prevent AMPAR desensitization, both greatly diminish inhibition of AMPARs by Ca2+. Cyclothiazide is more potent than aniracetam in both preventing of AMPAR desensitization and protecting against the Ca2+ inhibitory effect on hippocampal pyramidal cells. On giant cholinergic interneurones of striatum, aniracetam but not cyclothiazide significantly prevents inhibition by Ca2+. This agrees with available data on relative abundance of flip and flop splice variants in these cell types. The results suggest that Ca2+ may allosterically increase AMPA receptor desensitization independently on subunit composition and splice variants.
机译:在新鲜分离的大鼠脑神经元上研究了Ca2 +离子外部浓度(0.4-10 mM)变化对不同亚基组成的AMPA受体(AMPAR)的影响。 Ca2 +对AMPAR产生快速且可逆的电压依赖性抑制。 Ca2 +渗透性和Ca2 +不可渗透性AMPAR对外部Ca2 +同样敏感,表明该作用未针对离子通道。 AMPA引起的反应抑制作用明显大于海藻酸盐或谷氨酸引起的反应抑制作用。已知可以防止AMPAR脱敏的Cyclothiazide和阿尼西坦都大大减少了Ca2 +对AMPAR的抑制作用。在防止AMPAR脱敏和保护对海马锥体细胞的Ca2 +抑制作用方面,环丙咪嗪比阿尼西坦更有效。在纹状体的巨大胆碱能神经元上,阿尼西坦但不是环噻嗪明显阻止Ca 2+的抑制。这与关于这些细胞类型中的触发器和触发器剪接变体的相对丰度的可用数据一致。结果表明,Ca2 +可能独立于亚基组成和剪接变体而变构增加AMPA受体脱敏。

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