{"title":"大鼠脑图谱:胆碱乙酰转移酶的定量分布。","authors":"D Sutoo, K Yabe, K Akiyama","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>We have developed a fluorescence microphotometry system for microanalysis of the quantitative distribution of neurotransmitters and their related chemical substances in the brain slice. In the present study, the extensive distributions of cholinergic systems were analyzed quantitatively and in detail throughout the rat whole brains by this novel method through immunohistochemical staining of choline acetyltransferase (CAT). The rat whole brain was slice coronally and continuously, and 50 slices were chosen at approximately 500 microns intervals and stained immunohistochemically for CAT. Immunohistochemical fluorescence intensities were measured through a 6 microns phi (on the slice) pinhole of a microscope, the brain slice was moved along the X- or Y-axes stepwise at 40 microns intervals under the objective lens of the microscope, and the distributions of fluorescence intensities were analyzed over the entire surface of the slice. The brain was divided into approximately 5,000,000 areas, and immunohistochemical fluorescence intensities of those areas were quantitatively measured. The obtained fluorescence intensities of CAT were classified into 8 ranks and were indicated by color coding and by three-dimensional graphics. Also, the actual fluorescence intensity values in large brain regions were presented. This type of brain atlas of the neurotransmitter or its related chemical substances provides very important information on their dynamics in the brain under experimental as well as pathological conditions. 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In the present study, the extensive distributions of cholinergic systems were analyzed quantitatively and in detail throughout the rat whole brains by this novel method through immunohistochemical staining of choline acetyltransferase (CAT). The rat whole brain was slice coronally and continuously, and 50 slices were chosen at approximately 500 microns intervals and stained immunohistochemically for CAT. Immunohistochemical fluorescence intensities were measured through a 6 microns phi (on the slice) pinhole of a microscope, the brain slice was moved along the X- or Y-axes stepwise at 40 microns intervals under the objective lens of the microscope, and the distributions of fluorescence intensities were analyzed over the entire surface of the slice. The brain was divided into approximately 5,000,000 areas, and immunohistochemical fluorescence intensities of those areas were quantitatively measured. 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引用次数: 0
摘要
我们开发了一种荧光显微光度系统,用于微量分析脑切片中神经递质及其相关化学物质的定量分布。本研究通过对胆碱乙酰转移酶(choline acetyltransferase, CAT)的免疫组化染色,对大鼠全脑胆碱能系统的广泛分布进行了定量和详细的分析。取大鼠全脑冠状连续切片,间隔约500微米取50片,免疫组织化学染色进行CAT检测。通过显微镜6 μ m phi针孔测量免疫组织化学荧光强度,在显微镜物镜下沿X轴或y轴以40 μ m间隔逐步移动脑切片,分析整个切片表面荧光强度的分布。将大脑划分为约5,000,000个区域,定量测量这些区域的免疫组织化学荧光强度。得到的CAT荧光强度分为8个等级,用颜色编码和三维图形表示。同时给出了脑大区域的实际荧光强度值。这种类型的神经递质或其相关化学物质的脑图谱提供了它们在实验和病理条件下在大脑中的动态的非常重要的信息。此外,这种定量和详细的分析有助于将形态学数据与脑功能的神经化学和行为分析相结合。
Atlas of the rat brain: quantitative distribution of the choline acetyltransferase.
We have developed a fluorescence microphotometry system for microanalysis of the quantitative distribution of neurotransmitters and their related chemical substances in the brain slice. In the present study, the extensive distributions of cholinergic systems were analyzed quantitatively and in detail throughout the rat whole brains by this novel method through immunohistochemical staining of choline acetyltransferase (CAT). The rat whole brain was slice coronally and continuously, and 50 slices were chosen at approximately 500 microns intervals and stained immunohistochemically for CAT. Immunohistochemical fluorescence intensities were measured through a 6 microns phi (on the slice) pinhole of a microscope, the brain slice was moved along the X- or Y-axes stepwise at 40 microns intervals under the objective lens of the microscope, and the distributions of fluorescence intensities were analyzed over the entire surface of the slice. The brain was divided into approximately 5,000,000 areas, and immunohistochemical fluorescence intensities of those areas were quantitatively measured. The obtained fluorescence intensities of CAT were classified into 8 ranks and were indicated by color coding and by three-dimensional graphics. Also, the actual fluorescence intensity values in large brain regions were presented. This type of brain atlas of the neurotransmitter or its related chemical substances provides very important information on their dynamics in the brain under experimental as well as pathological conditions. Also, this quantitative and detailed analysis is useful for combining morphological data with those from neurochemical and behavioral analyses of brain function.