首页> 美国卫生研究院文献>The Journal of Physiology >Transcellular sodium fluxes and pump activity in Necturus gall-bladder epithelial cells.
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Transcellular sodium fluxes and pump activity in Necturus gall-bladder epithelial cells.

机译:Necturus胆囊上皮细胞中的跨细胞钠通量和泵浦活性。

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摘要

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.
机译:1.通过测量等渗流体流量确定Necturus中的上皮Na转运。在20℃下的速率等于175pmol cm-2 s-1。 2.瓦巴因在Necturus中是有效的,以5.4 X 10(3)M-1 s-1的平均速率常数与胆囊细胞中的Na泵结合。对[3H]哇巴因的自由空间的扩散时间常数的测量表明,当哇巴因在10(-3)M的浆膜上使用哇巴因时,泵必须在20 s内被完全抑制。3.负荷细胞的浆膜钠流出哇巴因对浓度为73 pmol cm-2 s-1的通量的抑制率为36%。剩余的通量不能归因于哇巴因引起的交换扩散或电扩散。 4.经上皮电位为0.3mV浆膜阳性。测得的短路电流为6.33 +/- 1.9 microA cm-2,等于65.6 pmol cm-2 s-1的正单价离子通量,或净Na转移的38%。 5 X 10(-5)M-阿米洛利可在1-5分钟内抑制电流。 5.哇巴因立即抑制了34%的液体分泌,相当于Na的等渗转运为59.7 pmol cm-2 s-1。此后持续至少一个小时,有时缓慢下降。阿米洛利几乎没有影响(13%)。 6.在哇巴因处理后的不同时间通过用示踪剂Na滴定细胞含量来测量Na泵浦速率。初始斜率等于时间为零时净通量的比率为61.6 pmol cm-2 s-1或35%。 7.还通过记录离子专用微电极记录的细胞Na活性升高并校正溶胀效应来测量Na泵速。 Na泵的速率与示踪剂Na含量的增加所估算的速率非常相似,等于59.3 pmol cm-2 s-1或跨上皮速率的31.4%。文献中对同一实验的检查显示出非常相似的值,约为流体分泌或净通量测量值的三分之一。 8.提出了一种方案来解释结果,该方案需要NaCl通过少量Na含量的平行途径流动,该途径涉及与细胞质Na在途中的交换。

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