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Membrane potential dependence of intracellular pH regulation by identified glial cells in the leech central nervous system.

机译:水identified中枢神经系统中已确定的神经胶质细胞对细胞内pH调节的膜电位依赖性。

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摘要

1. We have measured the intracellular pH (pHi) and membrane potential of identified glial cells in the central nervous system of the leech, Hirudo medicinalis, using double-barrelled pH-sensitive microelectrodes. 2. When extracellular K+ concentration was increased, the glial membrane potential decreased and pHi increased; lowering the extracellular K+ concentration hyperpolarized the glial membrane and decreased pHi. These pHi changes were largely dependent upon the presence of CO2-HCO3-; in nominally CO2-HCO3(-)-free saline solution, they were 50-80% smaller. 3. The steady-state pHi of the glial cells in CO2-HCO3(-)-buffered saline solution strongly correlated with the membrane potential between -40 and -90 mV. The slope of this relationship was 60 mV/pH unit. 4. The neurotransmitter 5-hydroxytryptamine (50 microM), which hyperpolarizes the glial membrane, also produced a large, CO2-HCO3(-)-dependent decrease in pHi. The size of the pHi change depended upon the amplitude of the membrane hyperpolarization. 5. The increase in pHi produced by the membrane depolarization in 20 mM-K+ was abolished in Na(+)-free saline. Removal of external Na+ in the presence of 20 mM-K+ reversed the pHi increase. 6. The pHi increase in 20 mM-K+ was also inhibited by the stilbene 4,4-diisothiocyanostilbene-2'-disulphonic acid (DIDS, 0.5 mM). In a DIDS-poisoned preparation a small decrease of pHi was observed in 20 mM-K+ both in the presence and nominal absence of CO2-HCO3-. 7. In neurones, neither CO2-HCO3- nor 20 mM-K+ produced an intracellular alkanization. The steady-state pHi of several identified neurones was not correlated with the membrane potential. 8. We conclude that in glial cells, but not in neurones, the pHi is dependent upon the membrane potential. This membrane potential dependence is due to the activity of the electrogenic Na(+)-HCO3- co-transporter in the glial cell membrane.
机译:1.我们使用双管pH敏感微电极测量了水ech中枢神经系统中已识别的神经胶质细胞的细胞内pH(pHi)和膜电位。 2.当细胞外钾离子浓度增加时,神经胶质膜电位降低,pHi增加;降低细胞外K +浓度会使神经胶质膜超极化并降低pHi。这些pHi变化在很大程度上取决于CO2-HCO3-的存在。在名义上不含CO2-HCO3(-)的盐溶液中,它们的体积要小50-80%。 3.在CO2-HCO3(-)缓冲盐溶液中,神经胶质细胞的稳态pHi与-40至-90 mV的膜电位密切相关。该关系的斜率是60mV / pH单位。 4.神经递质5-羟基色胺(50 microM)使神经胶质细胞膜超极化,也导致pHi的CO2-HCO3(-)依赖性大降低。 pHi变化的大小取决于膜超极化的幅度。 5.在无Na(+)的盐水中消除了在20 mM-K +中通过膜去极化产生的pHi的增加。在20 mM-K +存在下去除外部Na +可以逆转pHi的增加。 6. 1,2,4,4-二异硫氰酸氰基苯乙烯2'-二磺酸二苯乙烯(DIDS,0.5 mM)也抑制了20 mM-K +中pHi的增加。在DIDS中毒的制剂中,无论是否存在CO2-HCO3-,在20 mM-K +中均观察到pHi的小幅下降。 7.在神经元中,CO2-HCO3-或20 mM-K +均未产生细胞内烷化作用。几个确定的神经元的稳态pHi与膜电位无关。 8.我们得出结论,在神经胶质细胞中而不在神经元中,pHi取决于膜电位。这种膜电位依赖性是由于神经胶质细胞膜中的电致Na(+)-HCO3-共转运蛋白的活性所致。

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