Dodt H U, Zieglgänsberger W
Clinical Neuropharmacology, Max-Planck-Institute for Psychiatry, Munich, F.R.G.
Brain Res. 1990 Dec 24;537(1-2):333-6. doi: 10.1016/0006-8993(90)90380-t.
With a combination of infrared illumination, differential interference contrast (DIC) and image intensification by video, unstained living neurons have been visualized up to a depth of 50-100 microns in 300-microns thick brain slices. Recording and application pipettes could be placed under visual guidance. When applied to slices from rat neocortex and hippocampus, pyramidal and non-pyramidal neurons could be differentiated with medium magnification (20x-40x objective). Local neuronal clusters and bundling of apical dendrites of pyramidal cells were visible. The use of an objective with high numerical aperture (63x, N.A. 1.4) allowed the visualization of structures in the submicron range in neocortex and hippocampus. In combination with electrophysiological recordings, infrared DIC-videomicroscopy should facilitate the search for morphological changes underlying neuronal plasticity and the characterization of neuronal networks.
通过结合红外照明、微分干涉对比(DIC)和视频图像增强技术,在300微米厚的脑片中,未染色的活神经元已能在50至100微米的深度内被可视化。记录和应用移液管可以在视觉引导下放置。当应用于大鼠新皮层和海马体的切片时,中等放大倍数(20倍至40倍物镜)就能区分锥体细胞和非锥体细胞。局部神经元簇以及锥体细胞顶端树突的成束现象清晰可见。使用高数值孔径的物镜(63倍,N.A. 1.4)能够观察新皮层和海马体中亚微米级别的结构。结合电生理记录,红外DIC视频显微镜应有助于探寻神经元可塑性背后的形态学变化以及表征神经元网络。