Coronado R, Miller C
Nature. 1980 Dec 4;288(5790):495-7. doi: 10.1038/288495a0.
The sarcoplasmic reticulum membrane (SR) of skeletal muscle contains cation-selective channels which have been detected by isotope fluxes in fragmented SR vesicles, fluorimetric dyes and direct incorporation of SR vesicles to planar phospholipid bilayers. SR channels incorporated in bilayers have a single open-state conductance of 140 pS in 0.1 MK+ (refs 4,5). We have previously reported blockade of the SR channel by Cs+, a low-affinity blocker with a zero-voltage dissociation constant of 40 mM (ref. 6). We showed that increasing Cs+ concentrations reduced the open-channel conductance, increased the mean open time and conferred voltage dependence on the open-state conductance. Here we report on the blockade induced by the cholinergic drugs decamethonium and hexamethonium on the SR channel. Although blockade by hexamethonium is similar to that of Cs+, decamethonium blocks with a much higher affinity and induces flickering events which are probably due to the interaction of single drug molecules with the open state.
骨骼肌的肌浆网膜(SR)含有阳离子选择性通道,这些通道已通过同位素通量在破碎的SR囊泡中检测到,荧光染料以及将SR囊泡直接掺入平面磷脂双层中得以证实。掺入双层中的SR通道在0.1M K⁺中具有140 pS的单开放态电导(参考文献4,5)。我们之前报道过Cs⁺对SR通道的阻断作用,Cs⁺是一种低亲和力阻断剂,零电压解离常数为40 mM(参考文献6)。我们表明,增加Cs⁺浓度会降低开放通道的电导,增加平均开放时间,并使开放态电导具有电压依赖性。在此我们报告胆碱能药物十烃季铵和六甲季铵对SR通道的阻断作用。尽管六甲季铵的阻断作用与Cs⁺相似,但十烃季铵以更高的亲和力进行阻断,并诱导闪烁事件,这可能是由于单个药物分子与开放态相互作用所致。