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Consequences of CO2 acidosis for transmembrane Na+ transport and membrane current in rabbit cardiac Purkinje fibres.

机译:CO2酸中毒对兔心脏Purkinje纤维中跨膜Na +转运和膜电流的影响。

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摘要

1. The influence of sarcolemmal Na(+)-H+ exchange on intracellular Na+ activity (aiNa), intracellular pH (pHi) and membrane holding current (Ih) was investigated in rabbit cardiac Purkinje fibres. pHi and aiNa were measured with liquid sensor ion-selective microelectrodes. A two-microelectrode voltage clamp was used while recording pHi or aiNa.pHi was varied by alternating a nominally CO2-free HEPES buffer and a CO2-HCO3-buffer. 2. The intrinsic buffer capacity was calculated from the decrease in pHi after addition of CO2. The most accurate estimate was obtained when transmembrane pHi regulation was blocked and equalled 18.4 +/- 1.0 mequiv H+/pH unit (mean +/- S.E.M.). 3. aiNa started to rise when pHi fell below 7.0. A hyperpolarization paralleled the increase in aiNa. The magnitude of the rise in aiNa and the hyperpolarization were steeply dependent on pHi. 4. Inhibition of the Na(+)-K+ pump by K(+)-free superfusion increased aiNa. The rate of rise in aiNa was highly dependent on pHi. The rates of rise in 5% (pHi = 7.00 +/- 0.03), 7% (pHi = 6.89 +/- 0.04) and 15% CO2 (pHi = 6.74 +/- 0.02) at constant external pH (pHo) relative to the rate in HEPES solution (pHi = 7.24 +/- 0.02) were: 1.5 +/- 0.2, 2.4 +/- 0.1 and 3.1 +/- 0.2. The acid-induced rise in aiNa was abolished by 2 mM-amiloride. 5. Extracellular acidosis slowed down the recovery of pHi and depressed the rate of rise in aiNa upon intracellular acidification. When both pHi and pHo were decreased to 6.7 the acid-dependent rate increase fell to about 10% of the value found at pHo 7.4. 6. The tetrodotoxin (TTX)-sensitive Na+ current was not influenced by the change in pHi in the range 6.7-7.2. 7. Intracellular acidosis was associated with an early aiNa-independent depolarization and an inward shift in Ih. Current-voltage plots revealed that the initial inward current shift reversed at -81.5 mV on average, showed inward rectification and was largely depressed in the presence of 1 mM-Ba2+. These observations indicate a decrease in K+ conductance when pHi falls. 8. The increase in aiNa elicited a Na(+)-K+ pump-dependent outward current which could override the initial aiNa-independent current shift. At a pHo of 6.7 the initial fall in Ih remained, while the secondary outward current was largely depressed. 9. The rate of active Na+ extrusion and Na(+)-K+ pump current were suppressed by about 30% at pHi 6.7 compared to pHi 7.2.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.研究了兔心脏浦肯野纤维中肌膜Na(+)-H +交换对细胞内Na +活性(aiNa),细胞内pH(pHi)和膜保持电流(Ih)的影响。 pHi和aiNa用液体传感器离子选择性微电极测量。在记录pHi或aiNa的同时使用两电极电压钳。通过交替使用标称不含CO2的HEPES缓冲液和CO2-HCO3缓冲液来改变pHi。 2.根据添加CO2后pHi的降低来计算固有缓冲能力。当跨膜pHi调节受阻并等于18.4 +/- 1.0 mequiv H + / pH单位(平均值+/- S.E.M.)时,可获得最准确的估算值。 3.当pHi降至7.0以下时,aiNa开始升高。超极化与aiNa的增加平行。 aiNa的升高幅度和超极化现象严重依赖于pHi。 4.通过无K(+)的灌注抑制Na(+)-K +泵可增加aiNa。 aiNa的上升速率高度依赖于pHi。相对于恒定的外部pH(pHo),相对于恒定的外部pH(pHo),5%(pHi = 7.00 +/- 0.03),7%(pHi = 6.89 +/- 0.04)和15%CO2(pHi = 6.74 +/- 0.02)的上升速率在HEPES溶液中(pHi = 7.24 +/- 0.02)的比率为:1.5 +/- 0.2、2.4 +/- 0.1和3.1 +/- 0.2。 2 mM-阿米洛利消除了酸诱导的aiNa升高。 5.细胞外酸中毒减慢了pHi的恢复,并抑制了细胞内酸化后aiNa的上升速率。当pHi和pHo都降低到6.7时,酸依赖性速率的增加下降到pHo 7.4时的值的约10%。 6.河豚毒素(TTX)敏感的Na +电流不受pHi在6.7-7.2范围内变化的影响。 7.细胞内酸中毒与早期aiNa无关的去极化和Ih向内转移有关。电流-电压图显示,初始向内电流偏移平均在-81.5 mV处反转,显示向内整流,并在存在1 mM-Ba2 +的情况下被大大抑制。这些观察结果表明,当pHi下降时,K +电导降低。 8. aiNa的增加引起了Na(+)-K +泵相关的向外电流,该电流可能会超过aiNa无关的初始电流漂移。在6.7的pHo下,Ih的初始下降仍然存在,而次级的向外电流则大大降低了。 9.与pHi 7.2相比,在pHi 6.7时,活性Na +挤出速率和Na(+)-K +泵浦电流被抑制了约30%。(抽象截断为400字)

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