β—淀粉样蛋白31—35片段对海马神经元分离膜片Ca^2＋激活大电导钾通道的抑制

为了确定β－淀粉样蛋白（AβP）在影响神经元电生理特性并导致神经毒作用时的最短活性序列,实验采用片钳技术,在急性分离的大鼠海马CA1区锥体细胞的“内面向外”式膜片上,观察了AβP的31－35和25－35片段对C^2 a激活大电导钾（BK）通道活动的影响,结果显示,浴液中给预5umol/L的AβP31－35后,BK通道的平均开放概率（P0）和开放频率在1－3min内分别减少了85．8％（P＜0．01）和72．1％（P＜0．01）,平均开放时间减少了41．1％（P＜0．01）,平均电流幅度则无明显改变（P＞0．05）,给予同样摩尔浓度的AβP25－35后,BK通道平均P0减少了85．5％（P＜0．01）,平均开放时间减少51．4％,（P＜0．05）,结果提示：两种AβP片段对海马神经元BK通道具有抑制作用,。这可能与AβP的神经性作用有关,AβP－31－35片段可能是AβP分子中影响细胞电生理特性的最小活性序列。

Suppression of large conductance Ca2+-activated K+ channels by amyloid beta-protein fragment 31-35 in membrane patches excised from hippocampal neurons

To clarify the shortest essential active sequence in amyloid beta-protein (AbetaP) responsible for affecting neuronal electrophysiological properties, the effects of fragments 31-35 and 25-35 of AbetaP on the large conductance Ca(2+)-activated potassium (BK) channels were investigated in the "inside-out" membrane patches excised from hippocampal neurons of rats. After application of AbetaP 3l-35 (5 micromol/L, n=10), the mean P(o) and open frequency of BK channels decreased by 85.8+/-l3.5 percent;percent; (P<0.01) and 72.1+/-22.8 percent; (P<0.01), respectively, and the mean open time decreased by 41.l+/-l8.5 percent; (P<0.0l), while the mean current amplitude was not significantly affected (P>0.05). Application of AbetaP 25-35 (5 micromol/L) also induced a decrease of 85.5+/-22.l percent; (P<0.0l) in mean P(o) and of 5l.4+/-18.3 percent; (P<0.05) in mean open time within l~3 min after application. These results suggest that the functional alteration in BK channels elicited by AbetaP fragments may play an important role in the mechanisms underlying AbetaP neurotoxicity, and AbetaP 31-35 may be the shortest active sequence in AbetaP responsible for affecting the electrophysiological properties of neurons.