Dodt H U, Zieglgänsberger W
Max-Planck-Institute of Psychiatry, Clinical Institute, Clinical Neuropharmacology, Munich, Germany.
Histochem J. 1998 Mar;30(3):141-52. doi: 10.1023/a:1003291218707.
As a standard preparation for neurophysiological experiments, brain slices were introduced some 20 years ago. Although this technique has greatly advanced our understanding of brain physiology, the utility of this preparation has been limited to some extent by the difficulty of visualizing individual neurons in standard thick slices. The use of infrared videomicroscopy has solved this problem. It is now possible to visualize neurons in slices in great detail, and neuronal processes can be patch-clamped under visual control. Infrared videomicroscopy has also been applied successfully to other fields of neuroscience, such as neuronal development and neurotoxicity. A further development of infrared videomicroscopy allows the visualization of the spread of excitation in slices, making the technique a tool for investigating neuronal function and the pharmacology of synaptic transmission.
大约20年前,脑片被引入作为神经生理学实验的标准标本。尽管这项技术极大地增进了我们对脑生理学的理解,但由于在标准厚度的脑片中难以可视化单个神经元,该标本的实用性在一定程度上受到了限制。红外视频显微镜的应用解决了这个问题。现在可以非常详细地观察脑片中的神经元,并且可以在视觉控制下对神经元突起进行膜片钳记录。红外视频显微镜也已成功应用于神经科学的其他领域,如神经元发育和神经毒性研究。红外视频显微镜的进一步发展使得观察脑片中兴奋的传播成为可能,使该技术成为研究神经元功能和突触传递药理学的工具。