Quantitative measurement of reactive oxygen species in ex vivo mouse brain slices

被引:3
|
作者
Vasavda, Chirag [1 ]
Snyder, Solomon H. [1 ,2 ,3 ]
Paul, Bindu D. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
来源
STAR PROTOCOLS | 2021年 / 2卷 / 01期
关键词
LONG-TERM POTENTIATION; INTRACELLULAR SUPEROXIDE; HYDROETHIDINE; NEURODEGENERATION; PRODUCT; NEURONS; CORTEX; ANION; EDEMA; HPLC;
D O I
10.1016/j.xpro.2021.100332
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Evaluating redox homeostasis involves gauging the levels of reactive oxygen species (ROS) and reactive nitrogen species (RNS) directly in tissues and cells. The brain is especially metabolically active and is particularly vulnerable to excessive ROS and RNS. Here, we describe a methodology to quantitatively measure ROS in ex vivo mouse brain slices at baseline and after neural stimulation. Evaluating ROS in slices provides a more complete picture of neural redox signaling than when measured in isolated neurons or astrocytes.For complete details on the use and execution of this protocol, please refer to Vasavda et al. (2019).
引用
收藏
页数:17
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