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对冈田毒素类似物在修饰不同亚型青蛙钠通道时效力变化的分析。

An analysis of the variations in potency of grayanotoxin analogs in modifying frog sodium channels of differing subtypes.

作者信息

Yakehiro M, Yuki T, Yamaoka K, Furue T, Mori Y, Imoto K, Seyama I

机构信息

Division of Physiology, Department of Clinical Engineering, Hiroshima International University, Faculty of Health Sciences, Hiroshima, Japan.

出版信息

Mol Pharmacol. 2000 Oct;58(4):692-700. doi: 10.1124/mol.58.4.692.

Abstract

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.

摘要

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。

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