Tokimasa T
Department of Physiology, School of Medicine, Tokai University, Kanagawa, Japan.
Tokai J Exp Clin Med. 1995 Dec;20(4-6):227-32.
Whole-cell voltage-clamp recordings were made from cultured bullfrog dorsal root ganglion cells to examine the channel blocking activity of 20 microM of 1, 9-dideoxy forskolin (d-FSK) on the delayed rectifier potassium current. The drug reduced the maximum amplitude of the current (10-20 nA at +65 mV) by 40-80%. However, the voltages for 50%-activation (approximately -12 mV) and for 50%-inactivation (approximately -37 mV) remained unaffected by d-FSK. These results indicate that the channel block by d-FSK occurs in a voltage-independent manner.
采用全细胞膜片钳记录技术,对培养的牛蛙背根神经节细胞进行记录,以检测20微摩尔的1,9 - 二脱氧福斯高林(d - FSK)对延迟整流钾电流的通道阻断活性。该药物使电流的最大幅值(在+65毫伏时为10 - 20纳安)降低了40% - 80%。然而,50%激活电压(约 - 12毫伏)和50%失活电压(约 - 37毫伏)不受d - FSK影响。这些结果表明,d - FSK对通道的阻断以电压非依赖方式发生。