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[阿尔茨海默病的发病机制]

[Pathogenesis of Alzheimer's disease].

作者信息

Yuan J

出版信息

Zhonghua Yi Xue Za Zhi. 1990 Aug;70(8):429-30, 30.

PMID:2174279
Abstract

The 160 and 200 Kd phosphorylated and non-phosphorylated neurofilament monoclonal antibodies were used as the probe to study the cytoskeletal protein distribution inside cerebral neurons of 2 normal adults and 2 patients with Alzheimer's disease (AD). Immunocytochemical technique was applied in this study. Non-phosphorylated neurofilament was located in the perikarua, whereas, the phosphorylated neurofilament was rich in the peripheral of the neuron's cell body and axons in the normal adult brain. In AD, no significant difference was seen when non-phosphorylated neurofilament was compared with normal adult brain; but phosphorylated neurofilament was seen accumulated inside the neuron's cell bodies. We did not find any immunoreactivity of the above cytoskeletal proteins in the senile plaques. These results indicate that the accumulation of high molecular weight phosphorylated neurofilament inside the neuron's cell bodies is the early pathogenetic change of AD.

摘要

使用160和200千道尔顿的磷酸化和非磷酸化神经丝单克隆抗体作为探针,研究2名正常成年人和2名阿尔茨海默病(AD)患者大脑神经元内细胞骨架蛋白的分布。本研究采用免疫细胞化学技术。在正常成人大脑中,非磷酸化神经丝位于核周,而磷酸化神经丝在神经元胞体周围和轴突中丰富。在AD中,非磷酸化神经丝与正常成人大脑相比无显著差异;但可见磷酸化神经丝在神经元胞体内积聚。我们在老年斑中未发现上述细胞骨架蛋白的任何免疫反应性。这些结果表明,神经元胞体内高分子量磷酸化神经丝的积聚是AD的早期致病变化。

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