Suppr超能文献

衰老大脑和阿尔茨海默病大脑中血清蛋白的渗漏及神经元摄取。一种具有生前病因的死后现象。

Leakage and neuronal uptake of serum protein in aged and Alzheimer brains. A postmortem phenomenon with antemortem etiology.

作者信息

Mori S, Sternberger N H, Herman M M, Sternberger L A

机构信息

Department of Neurology, University of Maryland School of Medicine, Baltimore.

出版信息

Lab Invest. 1991 Mar;64(3):345-51.

PMID:2002653
Abstract

Abnormal extravasation of serum proteins has frequently been reported in Alzheimer's disease (AD) and less often in nondemented, aged individuals. In order to establish whether these are ante or postmortem phenomena, we have now compared the immunocytochemical localization of immunoglobulin in young, aged, and AD brains. In all the young brains, but only in some of the aged and AD brains, immunoglobulin was confined to a fine network of microvessels. In contrast, the majority of AD, as well as apparently normal, aged brains revealed both focal and diffuse extravascular localization in the form of neuronal labeling as well as a general, diffuse background. Since microvessels in these areas were no longer revealed, it was felt that the extravascular leakage occurred postmortem at a time when replacement of intravascular immunoglobulin had ceased. Furthermore, there was a correlation between the extent of leakage and time interval between death and autopsy. Postmortem leakage of serum protein was reproduced in a more controlled system using young and aged rats; serum protein leakage evolved from focal to diffuse patterns in aged brains as the postmortem period increased, whereas the leakage was restricted to the outer half of the cortices in young brains even after a prolonged postmortem period. Postmortem trauma to the rat brain also caused lesion-related leakage as well as neuronal labeling. It was concluded that extravascular leakage and neuronal uptake in aged and AD brains is a postmortem phenomenon, due to delay in autopsy or mishandling of brains, but dependent in severity upon antemortem circumstances.

摘要

血清蛋白异常外渗在阿尔茨海默病(AD)中经常被报道,而在非痴呆的老年人中则较少见。为了确定这些是生前还是死后现象,我们现在比较了免疫球蛋白在年轻、老年和AD大脑中的免疫细胞化学定位。在所有年轻大脑中,但仅在一些老年和AD大脑中,免疫球蛋白局限于微血管的精细网络。相比之下,大多数AD以及明显正常的老年大脑显示出以神经元标记形式存在的局灶性和弥漫性血管外定位以及普遍的弥漫性背景。由于这些区域的微血管不再显示,因此认为血管外渗漏发生在死后血管内免疫球蛋白替换停止的时候。此外,渗漏程度与死亡和尸检之间的时间间隔存在相关性。使用年轻和老年大鼠在一个更可控的系统中重现了血清蛋白的死后渗漏;随着死后时间的增加,老年大脑中的血清蛋白渗漏从局灶性发展为弥漫性模式,而即使在延长的死后时间后,年轻大脑中的渗漏也仅限于皮质的外半部分。对大鼠大脑的死后创伤也导致了与损伤相关的渗漏以及神经元标记。得出的结论是,老年和AD大脑中的血管外渗漏和神经元摄取是一种死后现象,这是由于尸检延迟或对大脑处理不当造成的,但严重程度取决于生前情况。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验