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正常海马及长期增强后NADPH-黄递酶的超微结构分布

Ultrastructural distribution of NADPH-diaphorase in the normal hippocampus and after long-term potentiation.

作者信息

Faber-Zuschratter H, Seidenbecher T, Reymann K, Wolf G

机构信息

Institute for Medical Neurobiology, University of Magdeburg, Federal Republic of Germany.

出版信息

J Neural Transm (Vienna). 1996;103(7):807-17. doi: 10.1007/BF01273359.

Abstract

The distribution of the enzyme nitric oxide synthase (NOS) was investigated at the ultrastructural level in synaptic structures of the hippocampal formation in relation to long-term potentiation (LTP), based on the histochemical NADPH-diaphorase (NADPH-d) staining with the tetrazolium salt BSPT. BSPT-formazan, the osmiophilic reaction product, was found to be selectively distributed and predominantly attached to membranes of the endoplasmic reticulum. In synaptic regions mainly the presynaptic sides showed labeling. Although several groups have demonstrated a principal involvement of NO in the LTP-mechanism, we found only a low, statistically insignificant increase in NADPH-d stained presynaptic areas of the dentate gyrus, where LTP was evoked. Postsynaptic elements also did not show any noticeable differences. Based on the present results, the predominantly presynaptic localization of NOS should be preferably considered in models describing a functional role of NO in LTP formation, despite the fact that we failed to reveal any indications for an LTP-related change in synaptically located NADPH-d.

摘要

基于用四唑盐BSPT进行的组织化学NADPH - 黄递酶(NADPH - d)染色,在超微结构水平上研究了海马结构突触结构中一氧化氮合酶(NOS)的分布与长时程增强(LTP)的关系。发现嗜锇反应产物BSPT - 甲臜选择性分布且主要附着在内质网的膜上。在突触区域,主要是突触前侧显示出标记。尽管有几个研究小组已经证明NO在LTP机制中起主要作用,但我们发现在诱发LTP的齿状回中,NADPH - d染色的突触前区域仅有少量增加,且在统计学上无显著意义。突触后成分也未显示出任何明显差异。基于目前的结果,尽管我们未能揭示突触定位的NADPH - d与LTP相关变化的任何迹象,但在描述NO在LTP形成中的功能作用的模型中,应优先考虑NOS主要位于突触前的定位情况。

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