Herdman P R, Taylor J J
Stain Technol. 1975 Jan;50(1):37-42. doi: 10.3109/10520297509117029.
A tissue pretreatment is introduced which effectively suppresses the silver impregnation of connective tissue and nonspecific background elements in peripheral nerve. The result is a selective impregnation of nerve fibers. The procedure utilizes fresh frozen sections and can be used with the Holmes (1947) or Bodian (1936) techniques. Fresh frozen sections are cut at 10 microns, mounted on slides and air dried for 5 minutes. They are fixed for 30 minutes in formol-sublimate (10% formalin saturated with mercuric chloride) and then placed into 0.5% iodine in 70% alcohol for 5 minutes followed by bleaching in 2.5% sodium thiosulfate for 2 minutes. After washing in running tap water for 10 minutes and a brief rinse in distilled water, impregnation is accomplished by the Holmes (1947) or Bodian (1936) procedure beginning with the step containing the aqueous silver solution. The results show an absence of impregnation of connective tissue and nonspecific background. The technique is simple, rapid, and, by utilizing fresh frozen sections, can be used for other histological and histochemical purposes. Several experiments were done to determine the causes of the connective tissue and background suppression. The air drying step was omitted; the sections were fixed in formalin without mercuric chloride; and the formol-sublimate fixation time was increased. The results suggest that connective tissue impregnation is suppressed by the use of mercuric chloride in the fixative and that the background suppression is related to the short fixation time with formolsublimate.
本文介绍了一种组织预处理方法,该方法能有效抑制周围神经中结缔组织和非特异性背景成分的银浸染。结果是神经纤维的选择性浸染。该程序使用新鲜冷冻切片,可与霍姆斯(1947年)或博迪安(1936年)技术一起使用。新鲜冷冻切片切成10微米厚,安装在载玻片上并空气干燥5分钟。它们在福尔马林-升汞(10%甲醛用氯化汞饱和)中固定30分钟,然后放入70%酒精中的0.5%碘溶液中5分钟,接着在2.5%硫代硫酸钠中漂白2分钟。在流水冲洗10分钟并在蒸馏水中短暂冲洗后,通过从含有银水溶液的步骤开始的霍姆斯(1947年)或博迪安(1936年)程序进行浸染。结果显示结缔组织和非特异性背景没有浸染。该技术简单、快速,并且通过使用新鲜冷冻切片,可用于其他组织学和组织化学目的。进行了几项实验以确定结缔组织和背景抑制的原因。省略了空气干燥步骤;切片在不含氯化汞的福尔马林中固定;并延长了福尔马林-升汞固定时间。结果表明,固定剂中使用氯化汞可抑制结缔组织浸染,背景抑制与福尔马林-升汞的短固定时间有关。