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阿尔茨海默病病理患者内嗅皮质中AMPA选择性谷氨酸受体亚基的减少:一项生化研究。

Reduction of AMPA-selective glutamate receptor subunits in the entorhinal cortex of patients with Alzheimer's disease pathology: a biochemical study.

作者信息

Yasuda R P, Ikonomovic M D, Sheffield R, Rubin R T, Wolfe B B, Armstrong D M

机构信息

Department of Pharmacology, Georgetown University, Washington, DC 20007, USA.

出版信息

Brain Res. 1995 Apr 24;678(1-2):161-7. doi: 10.1016/0006-8993(95)00178-s.

Abstract

Using biochemical techniques we determined concentrations of the AMPA-selective glutamate receptor subunits GluR1 and GluR2/3 in the entorhinal cortex of patients with Alzheimer's disease pathology and age-matched controls. Tangle density was also determined in anatomically matched samples and correlated with GluR1 and GluR2/3 receptor concentration. In Alzheimer's disease brain, Western blot analysis revealed average reductions of 43% and 38% for GluR1 and GluR2/3, respectively. Based on previous immunohistochemical studies, we infer that the majority of protein reduction was due to decreases in GluR1 and GluR2/3 immunolabeled elements in the more superficial layers of the entorhinal cortex (layers II and III). These layers of the entorhinal cortex contained numerous neurofibrillary tangles in Alzheimer's disease, but neither GluR1 nor GluR2/3 protein concentration correlated significantly with tangle density. We hypothesize that the decrease in specific glutamate receptor subunits, particularly GluR2/3, may contribute to the vulnerability of neurons in the entorhinal cortex via mechanisms involving calcium conductance through AMPA-selective channels.

摘要

我们运用生化技术测定了患有阿尔茨海默病病理改变的患者以及年龄匹配的对照者内嗅皮质中AMPA选择性谷氨酸受体亚基GluR1和GluR2/3的浓度。同时还在解剖学上匹配的样本中测定了缠结密度,并将其与GluR1和GluR2/3受体浓度进行关联分析。在阿尔茨海默病患者的大脑中,蛋白质印迹分析显示GluR1和GluR2/3的平均减少量分别为43%和38%。基于之前的免疫组织化学研究,我们推断蛋白质减少的主要原因是内嗅皮质较浅层(II层和III层)中GluR1和GluR2/3免疫标记元件的减少。在阿尔茨海默病中,内嗅皮质的这些层含有大量神经原纤维缠结,但GluR1和GluR2/3的蛋白质浓度均与缠结密度无显著相关性。我们推测特定谷氨酸受体亚基,尤其是GluR2/3的减少,可能通过涉及通过AMPA选择性通道的钙电导机制,导致内嗅皮质神经元的易损性。

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