Keenan C L, Chapman P F, Chang V C, Brown T H
Division of Neurosciences, Beckman Research Institute of the City of Hope, Duarte, CA 91010.
Brain Res Bull. 1988 Sep;21(3):373-83. doi: 10.1016/0361-9230(88)90149-9.
Video-enhanced contrast, differential-interference contrast microscopy (VEC-DICM) was used to visualize the cytoarchitecture and subcellular neuronal structure of acute brain slices from rat hippocampus and amygdala. Even at low-power magnification, the VEC-DICM system vastly improved our ability to visualize and examine the gross organization of the tissue. With medium-power magnification, the neuronal somata and proximal dendrites were clearly visible. With high-power magnification, some of the subcellular details could be clearly discerned--including cell nuclei, cell nucleoli, fine dendritic processes, and varicosities that may be synaptic expansions. We conclude that improved optical techniques should be valuable to cellular neurobiologists interested in structure-function relationships in brain slices.
视频增强对比度、微分干涉对比显微镜(VEC-DICM)被用于观察大鼠海马体和杏仁核急性脑切片的细胞结构和亚细胞神经元结构。即使在低倍放大倍数下,VEC-DICM系统也极大地提高了我们观察和检查组织总体结构的能力。在中倍放大倍数下,神经元胞体和近端树突清晰可见。在高倍放大倍数下,可以清楚地辨别一些亚细胞细节,包括细胞核、核仁、精细的树突状突起以及可能是突触膨大的静脉曲张。我们得出结论,改进的光学技术对于对脑切片结构-功能关系感兴趣的细胞神经生物学家应该是有价值的。