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美西螈胆囊上皮细胞中的跨细胞钠通量和泵活性。

Transcellular sodium fluxes and pump activity in Necturus gall-bladder epithelial cells.

作者信息

Hill A E, Hill B S

出版信息

J Physiol. 1987 Jan;382:35-49. doi: 10.1113/jphysiol.1987.sp016354.

Abstract
  1. Transepithelial Na transport in Necturus was determined by measuring the rate of isotonic fluid flow. The rate at 20 degrees C was equivalent to 175 pmol cm-2 s-1. 2. Ouabain was effective in Necturus, binding to the Na pump in gall-bladder cells with a mean rate constant of 5.4 X 10(3) M-1 s-1. Measurement of the diffusive time constant of the free space for [3H]ouabain shows that the pump must be fully inhibited within 20 s when ouabain is applied to the serosa at 10(-3) M. 3. The serosal Na efflux from loaded cells was inhibited 36% by ouabain equal to a flux of 73 pmol cm-2 s-1. The remaining flux could not be attributed to either exchange diffusion or electrodiffusion induced by ouabain. 4. The transepithelial potential was 0.3 mV serosa positive. The short-circuit current measured was 6.33 +/- 1.9 microA cm-2, equal to a positive univalent ion flux of 65.6 pmol cm-2 s-1 or 38% of the net Na transfer. The current was inhibited within 1-5 min by 5 X 10(-5) M-amiloride. 5. Fluid secretion was immediately inhibited 34% by ouabain, equivalent to an isotonic transport of Na of 59.7 pmol cm-2 s-1. Thereafter it continued for at least an hour, sometimes declining slowly. Amiloride had little effect (13%). 6. The Na pump rate was measured by titrating the cell content with tracer Na at different times after ouabain treatment. The initial slope was equal to a rate of 61.6 pmol cm-2 s-1 or 35% of the net flux at time zero. 7. The Na pump rate has also been measured by recording the rise in cell Na activity with ion-specific micro-electrodes, and correcting for swelling effects. The Na pump rate was very similar to that estimated from the rise in tracer Na content, equal to 59.3 pmol cm-2 s-1 or 31.4% of the transepithelial rate. Examination of the same experiment in the literature shows a closely similar value, about one-third of that expected from fluid secretion or net flux measurements. 8. A scheme is proposed to explain the results, which requires a flow of NaCl through a parallel pathway of small Na content involving exchange en route with the cytoplasmic Na.
摘要
  1. 通过测量等渗流体流动速率来测定美西螈的跨上皮钠转运。20℃时的速率相当于175皮摩尔·厘米⁻²·秒⁻¹。

  2. 哇巴因对美西螈有效,以平均速率常数5.4×10³M⁻¹·秒⁻¹与胆囊细胞中的钠泵结合。对[³H]哇巴因自由空间扩散时间常数的测量表明,当以10⁻³M的哇巴因施加于浆膜时,钠泵必须在20秒内被完全抑制。

  3. 哇巴因使负载细胞的浆膜钠外流受到36%的抑制,相当于73皮摩尔·厘米⁻²·秒⁻¹的通量。剩余通量不能归因于哇巴因诱导的交换扩散或电扩散。

  4. 跨上皮电位为浆膜侧正0.3毫伏。测得的短路电流为6.33±1.9微安·厘米⁻²,相当于65.6皮摩尔·厘米⁻²·秒⁻¹的正单价离子通量,或净钠转运的38%。该电流在1 - 5分钟内被5×10⁻⁵M的氨氯吡脒抑制。

  5. 哇巴因使液体分泌立即受到34%的抑制,相当于59.7皮摩尔·厘米⁻²·秒⁻¹的钠等渗转运。此后它至少持续一小时,有时缓慢下降。氨氯吡脒影响很小(13%)。

  6. 通过在哇巴因处理后的不同时间用示踪钠滴定细胞内容物来测量钠泵速率。初始斜率相当于61.6皮摩尔·厘米⁻²·秒⁻¹的速率,或零时净通量的35%。

  7. 也通过用离子特异性微电极记录细胞钠活性的升高并校正肿胀效应来测量钠泵速率。钠泵速率与根据示踪钠含量升高估计的值非常相似,相当于59.3皮摩尔·厘米⁻²·秒⁻¹,或跨上皮速率的31.4%。对文献中同一实验的研究表明有一个非常相似的值,约为液体分泌或净通量测量预期值的三分之一。

  8. 提出了一个方案来解释这些结果,该方案要求氯化钠通过一个小钠含量的平行途径流动,该途径在途中与细胞质钠进行交换。

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本文引用的文献

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Binding of the cardiac glycoside ouabain to intact cells.强心苷哇巴因与完整细胞的结合。
J Physiol. 1972 Jul;224(2):441-62. doi: 10.1113/jphysiol.1972.sp009904.

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