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The ionic mechanism of intracellular pH regulation in crayfish muscle fibres.

机译:小龙虾肌肉纤维中细胞内pH调节的离子机制。

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摘要

The ionic mechanism of intracellular pH (pHi) regulation was investigated in isolated muscle fibres of the carpopodite adductor in the crayfish Astacus fluviatilis by electrophysiological means with pH, Na+ and Cl- -sensitive liquid ion exchanger micro-electrodes. In eighty-six cells a mean pHi of 7.14 +/- 0.12 (S.D.) at a membrane potential of--79.7 +/- 3.4 mV was found under control conditions which is about one pH unit more alkaline than predicted from passive distribution and indicates the presence of an acid-extrusion mechanism. In order to study pHi recovery the cells were acid loaded by exposure either to NH4 Cl or CO2. The effects of HCO3- and DIDS (an inhibitor of the anion exchange) on pHi recovery as well as the HCO3- -dependent decrease of intracellular Cl- during pHi recovery indicate that in pHi regulation a mechanism of acid extrusion is involved which exchanges extracellular HCO3- for intracellular Cl-. In CO2/HCO3- -free solution or in salines with DIDS, pHi recovery was retarded to the same degree, but the effects were not additive. Because of this the remaining pHi recovery must originate from an HCO3- -independent acid-extrusion mechanism. In Na+ -free solution any pHi recovery was blocked; if pHi recovery occurred it was accompanied by an increase of intracellular Na+ activity (aiNa). From these results it was concluded that all acid extrusion mechanisms which contributed to pHi recovery are coupled to an influx of Na+. A Na+/H+/HCO3-/Cl-, and a separate Na+/H+, exchange are proposed as a model of pHi regulation in the crayfish muscle fibre. Similar kinds of acid extrusion mechanisms are found in the neurone of the crayfish (Moody, 1981), with the difference that in the muscle fibre pHi regulation is achieved mainly by the former process. The rate of pHi recovery is considerably lower in the muscle fibre than in the neurone or in the sensory cell (Moser, 1985) of crayfish.
机译:采用pH,Na +和Cl敏感的液体离子交换微电极,通过电生理学方法研究了小龙虾Astacus fluviatilis中腕足石加成物的分离肌纤维中细胞内pH(pHi)调节的离子机制。在八十六个电池中,在控制条件下,膜电位为--79.7 +/- 3.4 mV时,平均pHi为7.14 +/- 0.12(SD),比被动分布所预测的碱性值高约一个pH单位,这表明酸挤出机制的存在。为了研究pHi的回收,通过暴露于NH 4 Cl或CO 2来酸加载细胞。 HCO3-和DIDS(阴离子交换的抑制剂)对pHi回收以及pHi回收过程中细胞内Cl-的HCO3-依赖性降低的影响表明,在pHi调节中,涉及到酸挤出的机制与细胞外HCO3交换-用于细胞内Cl-。在不含CO2 / HCO3的溶液中或在含DIDS的盐水中,pHi的回收率被延迟到相同的程度,但这种作用不是累加的。因此,剩余的pHi回收必须源自不依赖HCO3的酸挤出机制。在不含Na +的溶液中,任何pHi的回收都被阻止;如果pHi恢复发生,则伴随着细胞内Na +活性(aiNa)的增加。从这些结果可以得出结论,所有有助于pHi回收的酸挤出机制都与Na +的涌入有关。 Na + / H + / HCO3- / Cl-和单独的Na + / H +交换被提出作为小龙虾肌肉纤维中pHi调节的模型。在小龙虾的神经元中发现了类似类型的酸挤压机制(Moody,1981),不同之处在于,肌肉纤维中pHi的调节主要是通过前一种过程来实现的。 pHi恢复率在小龙虾的肌肉纤维中比在神经元或小龙虾的感觉细胞中低(Moser,1985)。

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