Freund T F, Somogyi P
Neuroscience. 1983 Jul;9(3):463-74. doi: 10.1016/0306-4522(83)90166-5.
A method is described for impregnating neurons by the Golgi procedure in sections of brain tissue that are of a thickness 80-100 microns, so allowing a variety of histochemical procedures to be carried out prior to Golgi-impregnation. The method has been applied to the retina of the adult primate and to brain sections incubated to reveal horseradish peroxidase activity with substrates that give electron-dense reaction products. Sections containing neurons that have been filled with horseradish peroxidase by intracellular iontophoresis following electrophysiological characterization, or containing neurons retrogradely labelled by horseradish peroxidase, can be impregnated by this Golgi procedure. Subsequent gold-toning of the Golgi-impregnated neurons makes it possible to study, in the electron-microscope, both Golgi-impregnated and peroxidase-containing neurons and their afferent and efferent synaptic contacts within the same section. The procedure also makes it possible to repeat Golgi impregnation on sections already Golgi-impregnated and gold-toned, or to repeat the Golgi impregnation if the first impregnation is not satisfactory. The procedure is illustrated by examples from the monkey retina, cat visual cortex and rat neostriatum.
本文描述了一种通过高尔基氏法浸染脑组织切片中神经元的方法,该脑组织切片厚度为80 - 100微米,这样就可以在高尔基氏浸染之前进行多种组织化学程序。该方法已应用于成年灵长类动物的视网膜以及用能产生电子致密反应产物的底物孵育以显示辣根过氧化物酶活性的脑切片。在电生理特征化后通过细胞内离子电泳用辣根过氧化物酶填充的神经元切片,或含有经辣根过氧化物酶逆行标记的神经元的切片,都可以用这种高尔基氏法浸染。对高尔基氏浸染的神经元进行后续的金染色,使得在电子显微镜下能够在同一切片中研究高尔基氏浸染的神经元和含过氧化物酶的神经元及其传入和传出突触联系。该程序还使得能够对已经进行过高尔基氏浸染和金染色的切片重复进行高尔基氏浸染,或者如果第一次浸染不令人满意则重复进行高尔基氏浸染。文中通过来自猴视网膜、猫视觉皮层和大鼠新纹状体的例子对该程序进行了说明。