Slomianka L
Department of Neurobiology, Aarhus University, Denmark.
Neuroscience. 1992;48(2):325-52. doi: 10.1016/0306-4522(92)90494-m.
Recent methods allow the study of neurons that contain zinc in synaptic vesicles of their boutons (Timm-stainable boutons) by the intravital precipitation (local or throughout the CNS) of the vesicular zinc with selenium compounds and its subsequent retrograde transport to the parent neurons, where the precipitate can be silver enhanced. The present study is a description of the distribution of zinc-containing neurons, their possible connections and their terminal fields within the hippocampal region of the rat. Problems inherent to the methods are addressed. Finally, based on the results and a review of literature, the possible function of zinc in the hippocampal region is considered. Neurons which contain silver-enhanced precipitates were observed in layers II, V and VI of the lateral entorhinal area and in layers V and VI of the medial entorhinal area. In the parasubiculum, labeled cells were seen in layer II/III of the parasubiculum a and in layer V. Labeled cells in the presubiculum were concentrated in layers III and V, in the hippocampal pyramidal cell layer and the dentate granule cell layer, but neurons containing precipitates were largely absent from the subiculum. Zinc-containing axonal boutons defined subpopulations within principal hippocampal neuron populations. Within layer II of the lateral entorhinal cortex and the pyramidal cell layer for regio inferior deeply situated neurons were labeled, whereas superficially placed pyramidal cells were labeled in regio superior. The neuropil staining described in the present study corresponded to that found in earlier studies. However, glial and vascular staining or unspecific background were largely absent, and the neuropil staining could unequivocally be identified light microscopically. Methodological problems are most prominently reflected in unstained mossy fibers in some animals. Based on series from animals treated with decreasing doses of sodium selenite and increased survival times, this problem can be related to small amounts of circulating reactive selenium and a competition of zinc compartments (vesicles) for the selenium. Staining will fail where the competition prevents individual compartments from reaching a threshold amount of zinc precipitate for silver amplification. A guide to evaluate histological material is provided. The distribution of zinc-containing boutons and their cells of origin indicate that zinc-containing and zinc-negative projections are not organized as parallel pathways. The mossy fibers provide an example of a pure zinc-containing pathway. Projections from regio superior to the dorsal presubiculum are likely to be zinc-negative while projections from the same area to the subiculum are zinc-containing.(ABSTRACT TRUNCATED AT 400 WORDS)
最近的方法可以通过用硒化合物对囊泡锌进行活体沉淀(局部或整个中枢神经系统),并使其随后逆行运输到母神经元,在母神经元中沉淀可以进行银增强,从而研究其终扣(Timm染色阳性终扣)的突触小泡中含有锌的神经元。本研究描述了大鼠海马区域内含锌神经元的分布、它们可能的连接以及它们的终末野。文中讨论了该方法固有的问题。最后,基于研究结果并结合文献综述,探讨了锌在海马区域可能的功能。在外侧内嗅区的II、V和VI层以及内侧内嗅区的V和VI层观察到含有银增强沉淀的神经元。在副海马中,在副海马a的II/III层和V层发现了标记细胞。前海马中的标记细胞集中在III和V层、海马锥体细胞层和齿状颗粒细胞层,但下托中基本没有含有沉淀的神经元。含锌轴突终扣在主要海马神经元群体中定义了不同的亚群。在外侧内嗅皮质的II层和下区域的锥体细胞层中,深部的神经元被标记,而在上区域,浅层的锥体细胞被标记。本研究中描述的神经毡染色与早期研究结果一致。然而,基本没有胶质细胞和血管染色或非特异性背景,并且在光学显微镜下可以明确识别神经毡染色。方法学问题最突出地体现在一些动物中苔藓纤维未染色。根据用递减剂量亚硒酸钠处理并延长存活时间的动物系列研究,这个问题可能与少量循环的活性硒以及锌区室(囊泡)对硒的竞争有关。当这种竞争阻止单个区室达到银放大所需的锌沉淀阈值量时,染色就会失败。文中提供了评估组织学材料的指南。含锌终扣及其起源细胞的分布表明,含锌和不含锌的投射并非以平行通路的形式组织。苔藓纤维就是一条纯含锌通路的例子。从上区域到背侧前海马的投射可能不含锌,而从同一区域到下托的投射则含锌。(摘要截取自400字)