首页> 外文期刊>Journal of Neuroscience Methods >A simplified procedure for the physical development of the sulphide silver method to reveal synaptic zinc in combination with immunocytochemistry at light and electron microscopy.
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A simplified procedure for the physical development of the sulphide silver method to reveal synaptic zinc in combination with immunocytochemistry at light and electron microscopy.

机译:硫化银法物理开发的简化程序,可在光学和电子显微镜下结合免疫细胞化学揭示突触锌。

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摘要

The pool of zinc present in excitatory synaptic terminals in normal and pathological conditions (for instance the status epilepticus induced by kainic acid) can be stained by a silver sulphide method followed by physical development of the insoluble zinc-sulphide complexes. In this study we applied a previously described simple and rapid developing procedure that reveals synaptic zinc, to the study of normal and pathological hippocampi and combined it with pre and postembedding immunocytochemical methods to detect different antigens. Normal and kainic acid-treated rats were perfused with fixative solutions containing sodium sulphide and 50 microm-thick vibratome sections of the hippocampi were incubated in a commercial developing solution (IntenSE M, Amersham). The developed vibratome sections were then (1) mounted for light microscopy or osmicated and epon-embedded for electron microscopy; or (2) processed for the preembedding immunoenzymatic detection of various antigens (GABA, parvalbumin, calbindin) with light and electron microscopy. Thin sections from epon-embedded samples were also processed for the postembedding immunogold localization of glutamate. This very simple and rapid procedure gives rise to zinc-specific staining, comparable to that obtained with classical developing methods and good preservation of both antigenicity and ultrastructure. It is therefore possible to detect, in the same thick or thin section, zinc reaction product and different antigens.
机译:在正常和病理条件下(例如,由海藻酸引起的癫痫持续状态),存在于兴奋性突触末端的锌池可通过硫化银方法进行染色,然后物理开发不溶性的硫化锌复合物。在这项研究中,我们将先前描述的揭示突触锌的简单快速发展程序应用于正常和病理性海马体的研究,并将其与包埋前和包埋后免疫细胞化学方法相结合以检测不同的抗原。用含硫化钠的固定液灌注正常和海藻酸治疗的大鼠,将海马体的50微米厚的纤毛切片切入商业显影液(IntenSE M,Amersham)中。然后将显影的振动刀切片安装(1)进行光学显微镜检查或进行渗透处理,并进行电镜嵌入以进行电子显微镜检查;或(2)用光学和电子显微镜对各种抗原(GABA,小白蛋白,钙结合蛋白)进行包埋前免疫酶检测。还对来自epon嵌入样品的薄片进行了处理,以进行谷氨酸的嵌入后免疫金定位。这种非常简单和快速的过程可产生锌特异性染色,可与传统显影方法相比,并具有良好的抗原性和超微结构保存能力。因此,可以在相同的厚或薄切片中检测锌反应产物和不同的抗原。

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