谷氨酸摄取测定方案:体外和离体系统的剂量-反应和动力学分析

Q2 Pharmacology, Toxicology and Pharmaceutics
Andréia C. K. Fontana
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引用次数: 5

摘要

这篇文章介绍了程序的详细描述和基本的体外和离体摄取测定谷氨酸转运体的功能特征和化合物的作用,调节其活性的评估排除提示。检测是在短暂或稳定表达被研究的特定转运蛋白的细胞系、星形胶质细胞的原代培养物或内源性表达这些转运蛋白的离体突触体制剂中进行的。描述了两种主要的分析方法,包括测量测试化合物刺激或抑制功能的效力的剂量-反应分析(分别为EC50或IC50值)和计算放射标记底物摄取到细胞的表观亲和力(KM)和最大速度(Vmax)的动力学功能分析。所述方法以谷氨酸转运体为例;然而,该方案可以适用于使用其各自底物的其他神经递质转运体(例如,通过GATs摄取GABA,通过sert摄取血清素等)。©2018 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protocols for Measuring Glutamate Uptake: Dose-Response and Kinetic Assays in In Vitro and Ex Vivo Systems

This article presents detailed descriptions of procedures and troubleshooting tips for basic in vitro and ex vivo uptake assays for the functional characterization of glutamate transporters and the assessment of the effect of compounds that modulate their activity. Assays are performed in cell lines that transiently or stably express a particular transporter under investigation, in primary cultures of astrocytes, or in ex vivo synaptosomal preparations that endogenously express these transporters. Two main assays are described, including dose-response assays to measure potencies of test compounds for stimulation or inhibition of function (EC50 or IC50 values, respectively) and kinetic functional assays to calculate apparent affinity (KM) and maximal velocity (Vmax) of radiolabeled substrate uptake into the cells. The methods described use glutamate transporters as an example; however, the protocols can be adapted to other neurotransmitter transporters using their respective substrates (e.g., GABA uptake through GATs, serotonin uptake through SERTs, among others). © 2018 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Pharmacology
Current Protocols in Pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
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