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人类嗅黏膜中的锰超氧化物歧化酶和铜锌超氧化物歧化酶:在阿尔茨海默病中免疫反应性增加。

Manganese and copper-zinc superoxide dismutases in the human olfactory mucosa: increased immunoreactivity in Alzheimer's disease.

作者信息

Kulkarni-Narla A, Getchell T V, Schmitt F A, Getchell M L

机构信息

Department of Physiology, University of Kentucky College of Medicine, Lexington 40536, USA.

出版信息

Exp Neurol. 1996 Aug;140(2):115-25. doi: 10.1006/exnr.1996.0122.

DOI:10.1006/exnr.1996.0122
PMID:8690055
Abstract

Superoxide dismutases are the cell's major enzymatic defenses against cytotoxic reactive oxygen species and oxidative stress. Reactive oxygen species, which induce the expression of these enzymes, have been implicated in the neurodegeneration associated with Alzheimer's disease (AD), and individuals with AD exhibit early, severe deficits in olfactory ability. We used immunohistochemistry to examine the cellular localization of managanese and copper-zinc superoxide dismutases in the olfactory mucosae of nondemented young/middle-aged and old subjects as well as age-and postmortem-interval matched nondemented elderly individuals and those with AD. Tissues were obtained at autopsy from individuals ranging in age from 19 to 98 years old. Immunoreactivity for both enzymes was localized in olfactory receptor neurons, sustentacular and basal cells in the olfactory epithelium, and in olfactory and extrinsic nerves, Bowman's glands, and vascular endothelium in the lamina propria. Computer-assisted quantitative analysis demonstrated that very intense immunoreactivity for both managanese and copper-zinc superoxide dismutases occupied significantly more area, particularly near the surface and in the basal region, of the olfactory epithelium from subjects with AD than from the age-and postmortem interval-matched nondemented elderly subjects. The pronounced increase in superoxide dismutase immunoreactivity in the olfactory epithelium of AD subjects suggests that oxidative stress may be responsible, at least in part, for the olfactory deficits in subjects with AD.

摘要

超氧化物歧化酶是细胞抵御细胞毒性活性氧和氧化应激的主要酶性防御物质。诱导这些酶表达的活性氧与阿尔茨海默病(AD)相关的神经退行性变有关,且AD患者在嗅觉能力方面表现出早期严重缺陷。我们采用免疫组织化学方法,研究了锰超氧化物歧化酶和铜锌超氧化物歧化酶在未患痴呆的年轻/中年和老年受试者以及年龄和死后间隔匹配的未患痴呆的老年人和AD患者的嗅黏膜中的细胞定位。组织取自尸检的年龄在19至98岁的个体。两种酶的免疫反应性定位于嗅觉受体神经元、嗅上皮中的支持细胞和基底细胞,以及固有层中的嗅神经和外周末梢神经、鲍曼腺和血管内皮。计算机辅助定量分析表明,与年龄和死后间隔匹配的未患痴呆的老年受试者相比,AD患者嗅上皮中锰超氧化物歧化酶和铜锌超氧化物歧化酶的非常强烈的免疫反应性占据的面积显著更大,尤其是在靠近表面和基底区域。AD患者嗅上皮中超氧化物歧化酶免疫反应性的显著增加表明,氧化应激可能至少部分地导致了AD患者的嗅觉缺陷。

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Application of olfactory tissue and its neural progenitors to schizophrenia and psychiatric research.嗅觉组织及其神经祖细胞在精神分裂症和精神病学研究中的应用。
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