Russ U, Siemen D
Institut fur Zoologie, Universitat Regensburg, D-93040 Regensburg, Germany.
Pflugers Arch. 1996 Apr;431(6):888-94. doi: 10.1007/s004240050082.
Na+ and K+ currents were measured by the patch-clamp method in the paranodal region of single sciatic nerve fibres of rats and of warm-adapted and cold-adapted golden hamsters. Kinetic parameters and temperature dependence of the Na+ currents were determined. The time constant for activation (about 0.2 ms for rats and hamsters) as well as the time constant for inactivation (about 1.6 ms for rats and hamsters) at 15 degrees C and at -35 mV compared well with single fibre voltage-clamp data from the rat. Differences amongst the three groups of animals were not significant. The temperature coefficient, Q10, for the activation and the inactivation time constant as well as for the time-to-peak of the Na+ current ranged between 2.3 and 3.1. No data have previously been published on the temperature dependence of the delayed-rectifier K channels of mammalian nerve fibres. Most of the K+ current was carried by intermediate (KI) and fast (KF) K channels. Dendrotoxin block indicated that "approximate"55% of the K+ current was due to KI channels, with no significant difference amongst the three groups of animals tested. The Arrhenius plot of the time constant of K+ current activation, "tau"n, yielded a mean Q10 of 3.3 at -40 mV (4. 0 at + 60 mV). No significant differences of the channel kinetics between rats, warm-adapted hamsters and cold-adapted hamsters were detected. We observed, however, a significant decrease of the Na channel density in the paranodal region of cold-adapted hamsters.
采用膜片钳法在大鼠、暖适应和冷适应金黄地鼠的单根坐骨神经纤维的结旁区测量钠电流和钾电流。测定了钠电流的动力学参数及其温度依赖性。在15℃和-35mV时,激活时间常数(大鼠和地鼠约为0.2ms)以及失活时间常数(大鼠和地鼠约为1.6ms)与大鼠单纤维电压钳数据吻合良好。三组动物之间的差异不显著。钠电流激活和失活时间常数以及峰值时间的温度系数Q10在2.3至3.1之间。此前尚未发表关于哺乳动物神经纤维延迟整流钾通道温度依赖性的数据。大部分钾电流由中间(KI)和快速(KF)钾通道携带。树眼镜蛇毒素阻断表明,“大约”55%的钾电流归因于KI通道,在测试的三组动物之间没有显著差异。钾电流激活时间常数“τn”的阿伦尼乌斯曲线在-40mV时平均Q10为3.3(在+60mV时为4.0)。未检测到大鼠、暖适应地鼠和冷适应地鼠之间通道动力学的显著差异。然而,我们观察到冷适应地鼠结旁区钠通道密度显著降低。