首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Inhibition of ionic currents in frog node of Ranvier treated with naloxone.
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Inhibition of ionic currents in frog node of Ranvier treated with naloxone.

机译:纳洛酮处理的Ranvier蛙结中的离子流抑制作用。

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摘要

1 Myelinated nerve fibres of frog sciatic nerve were investigated under current and voltage clamp conditions. In the presence of 68 microM external naloxone, the action potential was completely, though progressively, blocked within 15 min of drug superfusion. The resting potential remained constant. 2 Under voltage clamp conditions both peak Na+ and steady-state K+ currents were decreased reversibly by external naloxone. Both currents were reduced in a dose-dependent manner but, whereas sodium current was affected by the smallest concentrations of naloxone (1.3 up to 12.5 microM), potassium current was decreased only by higher concentrations (25 up to 112 microM). 3 The time-course of development of the effect on both Na+ and K+ currents after exposure to 112 microM naloxone (a concentration giving more than 50% of decrease) showed that the effect develops quickly within the first 2 min of exposure to the drug, but afterwards both currents continue to fall more slowly, though progressively. 4 Experiments with constant test pulses to Em = - 10 mV and conditioning prepulses of various amplitudes, showed that the Na inactivation curve, h infinity (Em), was shifted in a negative direction along the potential axis; the shape of the curve was also slightly changed in the presence of naloxone since the shift was larger near the top of the curve. All the observed effects were reversible after returning to the standard Ringer solution. 5 Internal naloxone (less than 0.2 mM) reduced the amplitude of the action potential as well as peak Na+ and steady-state K+ currents; the sodium inactivation curve, h infinity (Em), was shifted to more negative potentials. 6 A possible anaesthetic-like activity of naloxone on the nodal membrane is discussed.
机译:1在电流和电压钳制条件下研究了青蛙坐骨神经的有髓神经纤维。在存在68 microM外部纳洛酮的情况下,药物逐渐融合的作用在15分钟内被完全(尽管被逐渐阻止)了。静息电位保持恒定。 2在电压钳制条件下,外部纳洛酮可逆地降低了峰值Na +和稳态K +电流。两种电流均以剂量依赖性方式降低,但是钠电流受最小浓度的纳洛酮(1.3至12.5 microM)影响,钾电流仅因较高浓度(25至112 microM)而降低。 3暴露于112 microM纳洛酮(浓度降低幅度超过50%)后,其对Na +和K +电流的影响随时间的发展过程表明,在暴露于该药物的前2分钟内,该作用迅速发展,但是此后,这两种电流的下降速度都在逐渐减小,尽管逐渐增大。 4在恒定测试脉冲为Em =-10 mV并调节各种幅度的预脉冲的实验中,发现Na灭活曲线h无穷大(Em)沿电势轴向负方向移动;在纳洛酮存在下,曲线的形状也略有变化,因为在曲线顶部附近的位移较大。回到标准林格溶液后,所有观察到的效果都是可逆的。 5内部纳洛酮(小于0.2 mM)降低了动作电位的幅度以及Na +和稳态K +峰值电流;钠灭活曲线h无穷大(Em)移到了更多的负电位。 6讨论了纳洛酮在淋巴结膜上可能的麻醉样活性。

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