Simmons M A, Schneider C R
Department of Pharmacology, Marshall University School of Medicine, Huntington, WV 25755-9310.
Neurosci Lett. 1993 Feb 19;150(2):133-6. doi: 10.1016/0304-3940(93)90519-q.
A peptide consisting of residues 25-35 of the amyloid beta protein was applied to single neurons while monitoring membrane current by whole cell voltage clamp recording. Within minutes of direct exposure of a neuron to the amyloid beta peptide, a paroxysmal increase in neuronal membrane conductance was observed. This conductance does not resemble previously described ionic conductances in terms of its time-dependence, voltage-dependence or sensitivity to changes in extracellular or intracellular ionic constituents. The effect of the amyloid beta peptide was not mimicked or blocked by substance P nor was it prevented by low intracellular or extracellular Ca. The increased membrane permeability elicited by the peptides may lead to the neuropathology observed in Alzheimer's disease.
将由β-淀粉样蛋白25 - 35位残基组成的肽应用于单个神经元,同时通过全细胞膜片钳记录监测膜电流。在神经元直接暴露于β-淀粉样肽几分钟内,观察到神经元膜电导阵发性增加。这种电导在时间依赖性、电压依赖性或对细胞外或细胞内离子成分变化的敏感性方面与先前描述的离子电导不同。P物质既不能模拟也不能阻断β-淀粉样肽的作用,低细胞内或细胞外钙也不能阻止其作用。这些肽引起的膜通透性增加可能导致阿尔茨海默病中观察到的神经病理学变化。