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阿尔茨海默病中乙酰胆碱丧失的胆碱渗漏假说。

The choline-leakage hypothesis for the loss of acetylcholine in Alzheimer's disease.

作者信息

Ehrenstein G, Galdzicki Z, Lange G D

机构信息

Biophysics Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Biophys J. 1997 Sep;73(3):1276-80. doi: 10.1016/S0006-3495(97)78160-8.

Abstract

We present a hypothesis for the loss of acetylcholine in Alzheimer's disease that is based on two recent experimental results: that beta-amyloid causes leakage of choline across cell membranes and that decreased production of acetylcholine increases the production of beta-amyloid. According to the hypothesis, an increase in beta-amyloid concentration caused by proteolysis of the amyloid precursor protein results in an increase in the leakage of choline out of cells. This leads to a reduction in intracellular choline concentration and hence a reduction in acetylcholine production. The reduction in acetylcholine production, in turn, causes an increase in the concentration of beta-amyloid. The resultant positive feedback between decreased acetylcholine and increased beta-amyloid accelerates the loss of acetylcholine. We compare the predictions of the choline-leakage hypothesis with a number of experimental observations. We also approximate it with a pair of ordinary differential equations. The solutions of these equations indicate that the loss of acetylcholine is very sensitive to the initial rate of beta-amyloid production.

摘要

我们基于最近的两个实验结果提出了一个关于阿尔茨海默病中乙酰胆碱缺失的假说

β-淀粉样蛋白会导致胆碱跨细胞膜泄漏,以及乙酰胆碱生成减少会增加β-淀粉样蛋白的生成。根据该假说,淀粉样前体蛋白的蛋白水解导致β-淀粉样蛋白浓度增加,进而导致胆碱从细胞中泄漏增加。这会导致细胞内胆碱浓度降低,从而使乙酰胆碱生成减少。乙酰胆碱生成的减少反过来又会导致β-淀粉样蛋白浓度增加。乙酰胆碱减少与β-淀粉样蛋白增加之间产生的正反馈加速了乙酰胆碱的缺失。我们将胆碱泄漏假说的预测与一些实验观察结果进行了比较。我们还用一对常微分方程对其进行了近似。这些方程的解表明,乙酰胆碱的缺失对β-淀粉样蛋白的初始生成速率非常敏感。

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