Furukawa K, Abe Y, Akaike N
Department of Neurophysiology, Tohoku University School of Medicine, Sendai, Japan.
Neuroreport. 1994 Oct 27;5(16):2016-8. doi: 10.1097/00001756-199410270-00006.
The effect of amyloid beta protein (A beta P) was examined in neurones dissociated from rat cortex using the nystatin perforated patch-clamp technique. A beta P at concentrations > 10 nM induced an irreversible slow inward current associated with an increase in membrane conductance. The time lag until the appearance of the effect of A beta P shortened in a concentration-dependent manner. When extracellular Na+ and Cl-, and intracellular K+ were replaced by equimolar N-methyl glucamine, isothionate- and Cs+, respectively, the membrane conductance and the reversal potential were not affected. Even when an internal solution including 1,2-bis(O-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (20 mM) was used, the effect of A beta P did not alter. It is suggested that A beta P binds to the neuronal membrane and opens non-selective ion channels, resulting in neuronal degeneration.
利用制霉菌素穿孔膜片钳技术,研究了β淀粉样蛋白(AβP)对从大鼠皮层分离出的神经元的影响。浓度大于10 nM的AβP会诱导出一种不可逆的缓慢内向电流,且伴有膜电导增加。AβP效应出现的时间延迟以浓度依赖的方式缩短。当细胞外的Na⁺和Cl⁻以及细胞内的K⁺分别被等摩尔的N - 甲基葡糖胺、异硫氰酸盐和Cs⁺替代时,膜电导和反转电位不受影响。即使使用包含1,2 - 双(O - 氨基苯氧基)乙烷 - N,N,N',N' - 四乙酸(20 mM)的内部溶液,AβP的效应也不会改变。提示AβP与神经元膜结合并打开非选择性离子通道,导致神经元变性。