Gonzalez-Lima F, Jones D
Institute for Neuroscience, University of Texas at Austin 78712.
Brain Res. 1994 Oct 10;660(1):34-49. doi: 10.1016/0006-8993(94)90836-2.
The objective was to obtain detailed topographic determinations of cytochrome oxidase activity in the gerbil central auditory system at the light microscopic level. Quantitative techniques were developed using (1) tissue standards calibrated to express histochemical measures as actual enzyme activity units, (2) densitometry and image analysis of histochemical reaction product formation, (3) spectrophotometry of cytochrome oxidase activity, and (4) a cobalt-intensified staining procedure compatible with autoradiography and other techniques requiring fresh-frozen brains without perfusion-fixation. Linear relationships between incubation time, section thickness, and activity of dissected brain regions, with their reaction product measured densitometrically were determined. Auditory structures with the high activities showed about 8 times the labeling intensity of the white matter or control sections inhibited with cyanide, glutaraldehyde, or heat. This indicated the high sensitivity of the method without loss of specificity. Specific activity for each of the 18 auditory structures measured were all above the units measured for whole brain homogenates, supporting the notion that basal levels of oxidative metabolism are greater for the auditory system. There was a progressive decrement in activity from brain stem to forebrain auditory structures. The more peripheral nuclei also showed a higher proportion of somatic as compared to neuropil reactivity. In contrast, auditory midbrain and thalamocortical regions were characterized primarily by neuropil reactivity. Comparison of intrinsic patterns of activity with morphological schemes to subdivide nuclei, showed a good correspondence with classical subdivisions derived from Golgi studies. The reported activities may provide a base of normative data in the gerbil for subsequent studies of central auditory functions. The method presented fulfilled established quantitative criteria and provided a more sensitive approach for regional mapping studies of brain cytochrome oxidase activity.
目的是在光镜水平上获得沙鼠中枢听觉系统中细胞色素氧化酶活性的详细地形图。开发了定量技术,包括:(1)校准组织标准,将组织化学测量值表示为实际酶活性单位;(2)对组织化学反应产物形成进行密度测定和图像分析;(3)对细胞色素氧化酶活性进行分光光度测定;(4)一种与放射自显影和其他需要新鲜冷冻脑且无需灌注固定的技术兼容的钴强化染色程序。确定了孵育时间、切片厚度与解剖脑区活性之间的线性关系,并通过密度测定法测量了它们的反应产物。具有高活性的听觉结构显示出的标记强度约为用氰化物、戊二醛或加热处理的白质或对照切片的8倍。这表明该方法具有高灵敏度且不失特异性。所测量的18个听觉结构中每个结构的比活性均高于全脑匀浆测量的单位,支持了听觉系统氧化代谢基础水平更高的观点。从脑干到前脑听觉结构的活性逐渐降低。与神经毡反应性相比,更外周的核团也显示出更高比例的体细胞反应性。相比之下,听觉中脑和丘脑皮质区域主要以神经毡反应性为特征。将内在活性模式与细分核团的形态学方案进行比较,发现与源自高尔基研究的经典细分有很好的对应关系。所报告的活性可能为沙鼠后续中枢听觉功能研究提供规范数据基础。所提出的方法满足既定的定量标准,并为脑细胞色素氧化酶活性的区域图谱研究提供了更灵敏的方法。