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绵羊心脏浦肯野纤维的细胞内钠活性:局部麻醉药和河豚毒素的作用。

The intracellular sodium activity of sheep heart Purkinje fibres: effects of local anaesthetics and tetrodotoxin.

作者信息

Deitmer J W, Ellis D

出版信息

J Physiol. 1980 Mar;300:269-82. doi: 10.1113/jphysiol.1980.sp013161.

Abstract
  1. The intracellular Na activity (a(Na) (i)) of quiescent sheep heart Purkinje fibres has been measured using Na(+)-sensitive glass micro-electrodes. The effects of local anaesthetics (procaine and lidocaine) and tetrodotoxin (TTX) have been investigated.2. Local anaesthetics reduced the steady-state level of the intracellular Na activity in a dose-dependent manner. The highest concentrations used (10(-2)M) reduced the intracellular Na activity by about 25%.3. TTX decreased the steady-state level of the intracellular Na activity. At a concentration of 10(-6) g/ml. (3.13 x 10(-6)M), TTX produced a decrease in intracellular Na activity of approximately 10%.4. The initial rate of rise of the intracellular Na activity upon addition of the cardioactive steroid strophanthidin (10(-5)M) was used to estimate the net passive Na influx.5. Procaine (5 x 10(-4)M) caused a 50% reduction of this rate of rise of the intracellular Na activity. The highest concentration of procaine used (10(-2)M) decreased the rate of rise by approximately 80%.6. Procaine (5 x 10(-3)M) also reduced the rate of rise of intracellular Na produced by the removal of external K (K(o)), and prevented the large depolarization associated with the absence of K(o).7. TTX also produced a decrease in the rate of rise of the intracellular Na activity that occurs upon addition of strophanthidin. A maximum effect was produced in our experiments at a TTX concentration of 10(-6) g/ml. At this concentration the rate of rise of intracellular Na activity was reduced by approximately 40% at a membrane potential of -70 mV.8. We conclude from our experiments that the effects of local anaesthetics and TTX on the intracellular Na activity are brought about by a reduction of the Na permeability of the cell membrane, and that at the normal resting potential, Na entry through TTX-sensitive channels contributes greatly to the total net Na influx.
摘要
  1. 利用钠敏感玻璃微电极测量了静态绵羊心脏浦肯野纤维的细胞内钠活性(a(Na)(i))。研究了局部麻醉药(普鲁卡因和利多卡因)和河豚毒素(TTX)的作用。

  2. 局部麻醉药以剂量依赖的方式降低细胞内钠活性的稳态水平。所使用的最高浓度(10(-2)M)使细胞内钠活性降低了约25%。

  3. TTX降低了细胞内钠活性的稳态水平。在浓度为10(-6) g/ml(3.13 x 10(-6)M)时,TTX使细胞内钠活性降低了约10%。

  4. 添加强心甾类毒毛花苷(10(-5)M)后细胞内钠活性的初始上升速率用于估计净被动钠内流。

  5. 普鲁卡因(5 x 10(-4)M)使细胞内钠活性的上升速率降低了50%。所使用的最高浓度普鲁卡因(10(-2)M)使上升速率降低了约80%。

  6. 普鲁卡因(5 x 10(-3)M)也降低了去除细胞外钾(K(o))所产生的细胞内钠上升速率,并防止了与缺乏K(o)相关的大去极化。

  7. TTX也使添加毒毛花苷时发生的细胞内钠活性上升速率降低。在我们的实验中,TTX浓度为10(-6) g/ml时产生最大效应。在此浓度下,在膜电位为-70 mV时,细胞内钠活性的上升速率降低了约40%。

  8. 我们从实验中得出结论,局部麻醉药和TTX对细胞内钠活性的影响是通过降低细胞膜的钠通透性实现的,并且在正常静息电位下,通过TTX敏感通道的钠内流对总净钠内流有很大贡献。

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Chloride ions and the membrane potential of Purkinje fibres.氯离子与浦肯野纤维的膜电位
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Cardiac arrhythmias complicating surgery.手术并发的心律失常
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