Mash D C, Flynn D D, Potter L T
Science. 1985 May 31;228(4703):1115-7. doi: 10.1126/science.3992249.
Cerebral cortex samples from patients with Alzheimer's disease and from rats after experimental cholinergic denervation of the cerebral cortex exhibited reductions in the presynaptic marker choline acetyltransferase activity and in the number of M2 muscarine receptors, with no change in the number of M1 receptors. These results are in keeping with evidence that M2 receptors function in cholinergic nerve terminals to regulate the release of acetylcholine, whereas M1 receptors are located on postsynaptic cells and facilitate cellular excitation. New M1-selective agonists and M2-selective antagonists directed at post- or presynaptic sites deserve consideration as potential agents for the treatment of the disease.
来自阿尔茨海默病患者以及大脑皮质经实验性胆碱能去神经支配的大鼠的大脑皮质样本,显示出突触前标志物胆碱乙酰转移酶活性降低以及M2毒蕈碱受体数量减少,而M1受体数量未发生变化。这些结果与以下证据一致:M2受体在胆碱能神经末梢发挥作用以调节乙酰胆碱的释放,而M1受体位于突触后细胞上并促进细胞兴奋。针对突触后或突触前位点的新型M1选择性激动剂和M2选择性拮抗剂值得作为该疾病的潜在治疗药物加以考虑。