Lippert Michael T, Takagaki Kentaroh, Xu Weifeng, Huang Xiaoying, Wu Jian-Young
Department of Physiology, Georgetown University Medical Center, Washington, DC 20057, USA.
J Neurophysiol. 2007 Jul;98(1):502-12. doi: 10.1152/jn.01169.2006. Epub 2007 May 9.
We describe methods to achieve high sensitivity in voltage-sensitive dye (VSD) imaging from rat barrel and visual cortices in vivo with the use of a blue dye RH1691 and a high dynamic range imaging device (photodiode array). With an improved staining protocol and an off-line procedure to remove pulsation artifact, the sensitivity of VSD recording is comparable with that of local field potential recording from the same location. With this sensitivity, one can record from approximately 500 individual detectors, each covering an area of cortical tissue 160 microm in diameter (total imaging field approximately 4 mm in diameter) and a temporal resolution of 1,600 frames/s, without multiple-trial averaging. We can record 80-100 trials of intermittent 10-s trials from each imaging field before the VSD signal reduces to one half of its initial amplitude because of bleaching and wash-out. Taken together, the methods described in this report provide a useful tool for visualizing evoked and spontaneous waves from rodent cortex.
我们描述了一些方法,可利用蓝色染料RH1691和高动态范围成像设备(光电二极管阵列),在活体大鼠的桶状皮质和视觉皮质中实现电压敏感染料(VSD)成像的高灵敏度。通过改进的染色方案和去除脉动伪影的离线程序,VSD记录的灵敏度与从同一位置进行的局部场电位记录相当。有了这种灵敏度,人们可以从大约500个单独的探测器进行记录,每个探测器覆盖直径为160微米的皮质组织区域(总成像场直径约为4毫米),时间分辨率为1600帧/秒,无需多次试验平均。在VSD信号因漂白和洗脱而降至其初始幅度的一半之前,我们可以从每个成像场记录80 - 100次间歇性的10秒试验。综上所述,本报告中描述的方法为可视化啮齿动物皮质中的诱发波和自发波提供了一个有用的工具。