Ehrenstein G, Galdzicki Z, Lange G D
Biophysics Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA.
Biophys J. 1997 Sep;73(3):1276-80. doi: 10.1016/S0006-3495(97)78160-8.
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.
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。