Su Z, Jiang S, Gu R
Institute of Otolaryngology, PLA General Hospital, Beijing.
Zhonghua Er Bi Yan Hou Ke Za Zhi. 1995;30(2):70-3.
In order to understand the cochlear physiology at a cellular and molecular level, Ca2+ channels were studied in cell-attached recordings from the basolateral membrane of the bullforg saccular hair cells with the EPC-9 patch-clamp system. Pipettes contained 110 mM Ba2+ and the membrane potential was zeroed with isotonic potassium aspartate. Data acquisition and analysis were performed using E9SCREEN and M2LAB software. L-type channel was distinguished by a single-channel conductance of 26 pS, activation range between -10 and +40 mV and intense activity even at a holding potential of -40 mV. The L-type channel showed characteristic bursts of brief openings (mode 1) interrupted occasionally by longer openings (mode 2). Bay K 8644 promoted the mode 2 activity and nifedipine inhibited L-type channel activity. Another type of calcium channels, 20 pS channel, was detected by -50 to +10 mV depolarizing steps from a holding potential of -40 mV or -80 mV. This channel was insensitive to dihydropyridines and resembled the N-type channel.
为了在细胞和分子水平上理解耳蜗生理学,使用EPC-9膜片钳系统,在牛蛙球囊毛细胞基底外侧膜的细胞贴附式记录中研究了Ca2+通道。微电极内含有110 mM Ba2+,膜电位用等渗天冬氨酸钾调零。使用E9SCREEN和M2LAB软件进行数据采集和分析。L型通道的单通道电导为26 pS,激活范围在-10至+40 mV之间,即使在-40 mV的钳制电位下也有强烈活动。L型通道表现出特征性的短暂开放爆发(模式1),偶尔被较长时间的开放(模式2)打断。Bay K 8644促进模式2活动,硝苯地平抑制L型通道活动。另一种钙通道,通过从-40 mV或-80 mV的钳制电位进行-50至+10 mV的去极化步骤检测到,单通道电导为20 pS。该通道对二氢吡啶不敏感,类似于N型通道。