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大鼠纹状体切片中[3H]半胱氨酸-3结合位点的快速体外调节

Rapid in vitro modulation of [3H]hemicholinium-3 binding sites in rat striatal slices.

作者信息

Saltarelli M D, Lowenstein P R, Coyle J T

出版信息

Eur J Pharmacol. 1987 Mar 3;135(1):35-40. doi: 10.1016/0014-2999(87)90754-0.

Abstract

The effects of depolarizing concentrations of potassium chloride on the modulation of [3H]hemicholinium-3 binding sites and high affinity choline uptake were examined in vitro. When rat striatal slices were incubated in Krebs buffer for 20 min, [3H]hemicholinium-3 binding sites diminished to 60% of binding measured in fresh un-incubated tissue, and remained stable for 60 min. Upon addition of Krebs buffer containing 40 mM KCl, the number of binding sites increased during a 20 min period, and remained stable for 40 min. Changes in [3H]hemicholinium-3 binding sites closely paralleled changes in high affinity choline uptake. Scatchard analysis revealed that changes in binding result from alterations in the number of binding sites (Bmax), and not in the affinity (KD). These results suggest that neuronal depolarization rapidly alters the velocity of choline transport into cholinergic neurons by increasing the number of available carriers.

摘要

在体外研究了去极化浓度的氯化钾对[3H]半胱氨酸-3结合位点调节和高亲和力胆碱摄取的影响。当大鼠纹状体切片在Krebs缓冲液中孵育20分钟时,[3H]半胱氨酸-3结合位点减少到新鲜未孵育组织中测量的结合量的60%,并在60分钟内保持稳定。加入含有40 mM KCl的Krebs缓冲液后,结合位点数量在20分钟内增加,并在40分钟内保持稳定。[3H]半胱氨酸-3结合位点的变化与高亲和力胆碱摄取的变化密切平行。Scatchard分析表明,结合变化是由结合位点数量(Bmax)的改变引起的,而不是亲和力(KD)的改变。这些结果表明,神经元去极化通过增加可用载体的数量,迅速改变胆碱转运到胆碱能神经元的速度。

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