Optogenetic field potential recording in cortical slices

被引:7
|
作者
Xiong, Wenhui [1 ]
Jin, Xiaoming [1 ]
机构
[1] Indiana Univ Sch Med, Stark Neurosci Res Inst, Dept Anat & Cell Biol, Indiana Spinal Cord & Brain Injury Res Grp, Indianapolis, IN 46202 USA
关键词
Field potential recording; Optogenetics; Channelrhodopsin-2; Cerebral cortex; Brain slice; Long-term depression; INJURED EPILEPTOGENIC NEOCORTEX; LONG-TERM POTENTIATION; TRANSGENIC MICE; SYNAPTIC CONNECTIVITY; NEURAL CIRCUITRY; VISUAL-CORTEX; CHANNELRHODOPSIN-2; HIPPOCAMPUS; ACTIVATION; NEURONS;
D O I
10.1016/j.jneumeth.2012.07.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We introduce a method that uses optogenetic stimulation to evoke field potentials in brain slices prepared from transgenic mice expressing channelrhodopsin-2-YFP. Cortical slices in a recording chamber were stimulated with a 473 nm blue laser via either a laser scanning photostimulation setup or by direct guidance of a fiber optic. Field potentials evoked by either of the two optogenetic stimulation methods had stable amplitude, consistent waveform, and similar components as events evoked with a conventional stimulating electrode. The amplitude of evoked excitatory postsynaptic potentials increased with increasing laser intensity or pulse duration. We further demonstrated that optogenetic stimulation can be used for the induction and monitoring of long-term depression. We conclude that this technique allows for efficient and reliable activation of field potentials in brain slice preparation, and will be useful for studying short and long term synaptic plasticity. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:119 / 124
页数:6
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