Yakehiro M, Yuki T, Yamaoka K, Furue T, Mori Y, Imoto K, Seyama I
Division of Physiology, Department of Clinical Engineering, Hiroshima International University, Faculty of Health Sciences, Hiroshima, Japan.
Mol Pharmacol. 2000 Oct;58(4):692-700. doi: 10.1124/mol.58.4.692.
Responses of tetrodotoxin-sensitive (TTX-s) and insensitive (TTX-i) Na(+) channels, in frog dorsal root ganglion (DRG) cells and frog heart Na(+) channels, to two grayanotoxin (GTX) analogs, GTX-I and alpha-dihydro-GTX-II, were examined using the patch clamp method. GTX-evoked modification occurred only when repetitive depolarizing pulses preceded a single test depolarization; modification, during the test pulse, was manifested by a decrease in peak Na(+) current accompanied by a sustained Na(+) current. GTX-evoked modification of whole-cell Na(+) currents was quantified by normalizing the conductance for sustained currents through GTX-modified Na(+) channels to that for the peak current through unmodified Na(+) channels. The dose-response relation for GTX-modified Na(+) channels was constructed by plotting the normalized slope conductance against GTX concentration. With respect to DRG TTX-i Na(+) channels, the EC(50) and maximal normalized slope conductance were estimated to be 31 microM and 0.23, respectively, for GTX-I, and 54 microM and 0.37, respectively, for alpha-dihydro-GTX-II. By contrast, TTX-s Na(+) channels in DRG cells and Na(+) channels in ventricular myocytes were found to have a much lower sensitivity to both GTX analogs. In single-channel recording on DRG cells and ventricular myocytes, Na(+) channels modified by the two GTX analogs (both at 100 microM), had similar relative conductances (range, 0.25-0.42) and open channel probabilities (range, 0.5-0.71). From these observations, we conclude that the differences in responsiveness of DRG TTX-i, and ventricular whole cell Na(+) currents to the GTX analogs studied are related to the number of Na(+) channels modified.
采用膜片钳方法,研究了青蛙背根神经节(DRG)细胞中对河豚毒素敏感(TTX-s)和不敏感(TTX-i)的Na⁺通道以及青蛙心脏Na⁺通道对两种冈田毒素(GTX)类似物GTX-I和α-二氢-GTX-II的反应。只有在单个测试去极化之前施加重复去极化脉冲时,才会发生GTX诱发的修饰;在测试脉冲期间,修饰表现为Na⁺电流峰值降低并伴有持续的Na⁺电流。通过将经GTX修饰的Na⁺通道的持续电流电导与未经修饰的Na⁺通道的峰值电流电导进行归一化,对全细胞Na⁺电流的GTX诱发修饰进行定量。通过绘制归一化斜率电导与GTX浓度的关系图,构建了GTX修饰的Na⁺通道的剂量反应关系。对于DRG TTX-i Na⁺通道,GTX-I的半数有效浓度(EC₅₀)和最大归一化斜率电导分别估计为31μM和0.23,α-二氢-GTX-II分别为54μM和0.37。相比之下,发现DRG细胞中的TTX-s Na⁺通道和心室肌细胞中的Na⁺通道对这两种GTX类似物的敏感性要低得多。在DRG细胞和心室肌细胞的单通道记录中,被两种GTX类似物(均为100μM)修饰的Na⁺通道具有相似的相对电导(范围为0.25 - 0.42)和开放通道概率(范围为0.5 - 0.71)。从这些观察结果中,我们得出结论,DRG TTX-i和心室全细胞Na⁺电流对所研究的GTX类似物反应性的差异与被修饰的Na⁺通道数量有关。