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美西螈视神经胶质细胞中电生性Na⁺/HCO₃⁻协同转运的进一步研究:细胞内pH的调节

Further studies of electrogenic Na+/HCO3- cotransport in glial cells of Necturus optic nerve: regulation of pHi.

作者信息

Astion M L, Chvatal A, Orkand R K

机构信息

Institute of Neurobiology, University of Puerto Rico, Old San Juan 00901.

出版信息

Glia. 1991;4(5):461-8. doi: 10.1002/glia.440040506.

DOI:10.1002/glia.440040506
PMID:1834563
Abstract

In the presence of Ba++, an increase in the bath HCO3- at constant CO2 (i.e., variable bath pH) produced a hyperpolarization. The hyperpolarizing effect of adding HCO3-/CO2 at constant bath pH was not significantly affected by the presence of 50 mumol/l strophanthidin. In the absence of Ba++, addition of HCO3-/CO2 at constant bath pH produced a Na(+)-dependent hyperpolarization. Therefore, CO2 movements, electrogenic Na+/K+ pump activity and changes in Ba++ binding do not contribute significantly to the hyperpolarization induced by HCO3-. These results along with the results of previous studies (Astion et al: J Gen Physiol 93:731, 1989) strongly suggest that the hyperpolarization induced by the addition of HCO3- is due to an electrogenic Na+/HCO3- cotransporter, which transports Na+, HCO3- (or its equivalent), and net negative charge across the glial membrane. To study the role of electrogenic Na+/HCO3- cotransport in the regulation of pHi in glial cells, we used intracellular double-barreled, pH-sensitive microelectrodes. At a bath pH of 7.5, the mean initial intracellular pH (pHi) was 7.32 (SD 0.03, n = 6) in HEPES-buffered Ringer's solution and 7.39 (SD 0.1, n = 6) in HCO3-/CO2 buffered solution. These values for pHi are more than 1.2 pH units alkaline to the pHi predicted from a passive distribution of protons; thus, these cells actively regulate pHi. Superfusion and withdrawal of 15 mmol/l NH4+ induced an acidification of 0.2 to 0.3 pH units, which recovered toward the original steady-state pHi.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在存在Ba++的情况下,在恒定CO2(即浴液pH可变)时增加浴液中的HCO3-会产生超极化。在恒定浴液pH下添加HCO3-/CO2的超极化作用不受50 μmol/l毒毛花苷的显著影响。在不存在Ba++的情况下,在恒定浴液pH下添加HCO3-/CO2会产生Na(+)依赖性超极化。因此,CO2移动、电生性Na+/K+泵活性以及Ba++结合的变化对HCO3-诱导的超极化作用不显著。这些结果以及先前研究(阿斯蒂翁等人:《普通生理学杂志》93:731,1989)的结果强烈表明,添加HCO3-诱导的超极化是由于电生性Na+/HCO3-共转运体,该共转运体跨胶质细胞膜转运Na+、HCO3-(或其等价物)和净负电荷。为了研究电生性Na+/HCO3-共转运在胶质细胞内pH(pHi)调节中的作用,我们使用了细胞内双管pH敏感微电极。在浴液pH为7.5时,在HEPES缓冲的林格氏溶液中,平均初始细胞内pH(pHi)为7.32(标准差0.03,n = 6),在HCO3-/CO2缓冲溶液中为7.39(标准差0.1,n = 6)。这些pHi值比根据质子被动分布预测的pHi碱性高1.2个以上pH单位;因此,这些细胞能主动调节pHi。用15 mmol/l NH4+进行灌流和撤流会导致酸化0.2至0.3个pH单位,随后恢复到原来的稳态pHi。(摘要截短于250字)

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