Switzer R C
NeuroScience Associates, Knoxville, Tennessee 37922, USA.
Toxicol Pathol. 2000 Jan-Feb;28(1):70-83. doi: 10.1177/019262330002800109.
Silver staining procedures have been used in numerous ways to render a variety of physical and biological features visible. In biological tissue, histologic protocols use silver to visualize diverse structures or features, such as reticulin, melanin, fungi, chromosome bands, nucleolar organizing regions, and different features in the nervous system. A comparison of the specific steps in these protocols indicates that the silver is "directed" to stain any given feature by the type of fixation, the pretreatment ("mordanting"), the composition of the silver-containing solution(s), and the form of development (reduction). Since the mechanisms of staining have not been understood historically (nor are they now), each method was developed by trial and error. Keystone methods such as those of Bodian and Bielschowsky exploit the nervous system's affinity for silver (argyrophilia). The beginning of a new era in brain research came with the recognition that distinct silver-impregnated morphologic changes occurring in damaged axons could be used for tracing axon pathways in experimental animals with specifically placed lesions. Improvements in staining methods used to selectively impregnate the disintegrating axons but to leave normal axons unstained were achieved by Nauta and Gygax (early workers with these procedures) and spawned a host of method variations known as the "Nauta" methods. Of these, the Fink-Heimer and de Olmos cupric-silver methods were able to unambiguously demonstrate disintegrating synaptic terminals, thereby allowing complete tracing of axon pathways. The late 1970s and 1980s witnessed innovative applications of these techniques. The silver methods once used to trace axon pathways became indicators of the extreme endpoint of neurotoxicity: disintegrative degeneration of neurons induced by neurotoxic chemicals that were administered systemically. The hallmark of neurotoxic substances is the selectivity with which each destroys specific populations or subpopulations of neurons. The high contrast and sensitivity of the silver degeneration stains greatly facilitate the screening process to detect these affected populations, especially when there is no basis for knowing where in the brain to look for damage. More recently, in addition to expanded use in screening for neurotoxic effects, the silver degeneration stains are being used to chart the neuron populations undergoing programmed cell death in the developing brain. Other newly developed silver methods have been refined to show nondisintegrative degeneration, such as the plaques,and tangles of Alzheimer's disease.
银染程序已被广泛应用于多种方式,以使各种物理和生物学特征可见。在生物组织中,组织学方案使用银来可视化各种结构或特征,如网状纤维、黑色素、真菌、染色体带、核仁组织区以及神经系统中的不同特征。对这些方案中具体步骤的比较表明,通过固定类型、预处理(“媒染”)、含银溶液的成分以及显影形式(还原),银被“引导”去染色任何给定的特征。由于染色机制在历史上(现在也未)被理解,每种方法都是通过反复试验开发出来的。像博迪安和 Bielschowsky 方法这样的关键方法利用了神经系统对银的亲和力(嗜银性)。脑研究新时代的开端是人们认识到,受损轴突中出现的独特银浸染形态变化可用于追踪实验动物中特定部位损伤后的轴突路径。瑙塔和吉加克斯(这些程序的早期工作者)改进了用于选择性浸染解体轴突但使正常轴突不染色的染色方法,并催生了许多被称为“瑙塔”方法的变体。其中,芬克 - 海默和德奥尔莫斯的铜银方法能够明确显示解体的突触终末,从而实现对轴突路径的完整追踪。20世纪70年代末和80年代见证了这些技术的创新应用。曾经用于追踪轴突路径的银方法成为了神经毒性极端终点的指标:全身给药的神经毒性化学物质诱导的神经元解体性退变。神经毒性物质的标志是每种物质对特定神经元群体或亚群体的选择性破坏。银染退变染色的高对比度和敏感性极大地促进了检测这些受影响群体的筛选过程,特别是在没有依据知道大脑中何处会出现损伤的情况下。最近,除了在神经毒性效应筛选中的应用扩展外,银染退变染色还被用于绘制发育中大脑中正在经历程序性细胞死亡的神经元群体。其他新开发的银方法已得到改进以显示非解体性退变,如阿尔茨海默病的斑块和缠结。