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钠氢交换对绵羊心脏浦肯野纤维细胞内pH值、钠含量和张力的影响。

Influence of sodium-hydrogen exchange on intracellular pH, sodium and tension in sheep cardiac Purkinje fibres.

作者信息

Kaila K, Vaughan-Jones R D

机构信息

University Laboratory of Physiology, Oxford.

出版信息

J Physiol. 1987 Sep;390:93-118. doi: 10.1113/jphysiol.1987.sp016688.

DOI:10.1113/jphysiol.1987.sp016688
PMID:2451001
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1192168/
Abstract
  1. The influence of sarcolemmal Na+-H+ exchange upon intracellular Na+ activity (aiNa), intracellular pH (pHi), extracellular surface pH (pHs) and tonic tension was investigated in sheep cardiac Purkinje fibres. Intracellular ion activities were measured with liquid sensor ion-selective micro-electrodes. A two-micro-electrode voltage-clamp was also used to control membrane potential while simultaneously recording tonic tension. 2. Inhibition of the sarcolemmal Na+-K+ pump by strophanthidin (10 mumol/l) produced a rise in aiNa, an increase in [Ca2+]i as evidenced by a rise in tonic tension, and a fall in pHi of 0.1-0.3 units. The intracellular acidosis has been shown previously to be linked to the rise in [Ca2+]i (Vaughan-Jones, Lederer & Eisner, 1983). 3. Amiloride (1-2 mmol/l), an inhibitor of Na+-H+ exchange, produced a small reversible decrease in pHi and aiNa. Both effects became more pronounced in strophanthidin-exposed fibres. In addition, pHi decreased during application of strophanthidin and this decrease was reversibly inhibited by amiloride. It is concluded that sarcolemmal Na+-H+ exchange is stimulated following inhibition of the Na+-K+ pump. 4. In strophanthidin-exposed fibres, a rise in [Ca2+]i resulted in an intracellular acidosis which could still be observed in the presence of amiloride (1 mmol/l). This suggests that the fall in pHi was not caused by a modulatory effect of [Ca2+]i on sarcolemmal Na+-H+ exchange. 5. Tetrodotoxin (TTX) produced a small fall in aiNa (ca. 0.5 mmol/l) which was not augmented in the presence of strophanthidin. Furthermore, the effects on aiNa of TTX and amiloride were additive. Thus the influence of amiloride on aiNa does not involve blockade of voltage-gated Na+ channels. 6. The stoicheiometry of Na+-H+ exchange, estimated from the rates of change of pHi and aiNa in amiloride, appeared to be electroneutral (1:1). The stoicheiometry was unaffected by changes in pHi. 7. In strophanthidin-exposed fibres (i.e. aiNa is elevated), the recovery of pHi from an intracellular acidosis (brought about by brief exposure to NH4Cl) was slowed greatly by amiloride (1-2 mmol/l). The rise in aiNa that occurred during pHi recovery was also reduced by amiloride. It is concluded that Na+-H+ exchange can be stimulated by a fall in pHi under conditions where aiNa is elevated. However, at a given pHi, its rate of recovery was slower in the presence than in the absence of strophanthidin.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在绵羊心脏浦肯野纤维中,研究了肌膜钠氢交换对细胞内钠活性(aiNa)、细胞内pH值(pHi)、细胞外表面pH值(pHs)和张力的影响。用液体传感器离子选择性微电极测量细胞内离子活性。还使用双微电极电压钳来控制膜电位,同时记录张力。2. 毒毛花苷(10 μmol/l)抑制肌膜钠钾泵后,aiNa升高,张力增加表明细胞内[Ca2+]i升高,pHi下降0.1 - 0.3个单位。先前已表明细胞内酸中毒与[Ca2+]i升高有关(沃恩 - 琼斯、莱德勒和艾斯纳,1983年)。3. 钠氢交换抑制剂氨氯地平(1 - 2 mmol/l)使pHi和aiNa出现小幅度可逆性下降。在毒毛花苷处理的纤维中,这两种效应更明显。此外,毒毛花苷应用期间pHi下降,氨氯地平可使其可逆性抑制。结论是钠钾泵抑制后肌膜钠氢交换被刺激。4. 在毒毛花苷处理的纤维中,[Ca2+]i升高导致细胞内酸中毒,在存在氨氯地平(1 mmol/l)时仍可观察到。这表明pHi下降不是由[Ca2+]i对肌膜钠氢交换的调节作用引起的。5. 河豚毒素(TTX)使aiNa小幅下降(约0.5 mmol/l),在存在毒毛花苷时并未增强。此外,TTX和氨氯地平对aiNa的作用是相加的。因此,氨氯地平对aiNa的影响不涉及电压门控钠通道的阻断。6. 根据氨氯地平作用下pHi和aiNa的变化率估算的钠氢交换化学计量比似乎是电中性的(1:1)。化学计量比不受pHi变化的影响。7. 在毒毛花苷处理的纤维中(即aiNa升高),氨氯地平(1 - 2 mmol/l)极大地减缓了细胞内酸中毒(由短暂暴露于氯化铵引起)后pHi的恢复。pHi恢复期间出现的aiNa升高也被氨氯地平降低。结论是在aiNa升高的情况下,pHi下降可刺激钠氢交换。然而,在给定的pHi下,存在毒毛花苷时其恢复速率比不存在时更慢。(摘要截取自400字)

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本文引用的文献

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Interactions between the regulation of the intracellular pH and sodium activity of sheep cardiac Purkinje fibres.绵羊心脏浦肯野纤维细胞内pH调节与钠活性之间的相互作用。
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Intracellular pH and surface pH in skeletal and cardiac muscle measured with a double-barrelled pH microelectrode.用双管pH微电极测量骨骼肌和心肌中的细胞内pH值和表面pH值。
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