Abstract
1. We have used double-barrelled ion-sensitive microelectrodes to measure the intracellular pH, pHi, the intracellular Na+ activity, aiNa, and the membrane potential in identified glial cells of the central nervous system of the leech Hirudo medicinalis to study the effect of CO2-HCO3-. 2. When a HEPES-buffered saline was exchanged for a saline buffered with 2% CO2 + 11 mM-HCO3-, keeping the pH constant at 7.4, the mean steady-state pHi of the glial cells increased from 6.85 +/- 0.06 to 7.18 +/- 0.13 (mean +/- S.D., n = 25). 3. This CO2-HCO3- -dependent alkalinization was inhibited in the absence of external Na+ (exchanged by N-methyl-D-glucamine), but was unaffected by the inhibitor of Na+-H+ exchange, amiloride (2 mM). 4. The aiNa of the glial cells increased by 2-4 mM from a mean steady state of 7.2 +/- 2 mM (mean +/- S.D., n = 6) upon introduction of CO2-HCO3- -buffered saline. This CO2-HCO3- -dependent rise in aiNa increased to about double when the pHi had been decreased by acid loading the cells (addition and subsequent removal of NH4+). 5. The CO2-HCO3- -dependent increases of pHi and aiNa were inhibited by the stilbene 4,4-diisothiocyanostilbene-2,2'-disulphonic acid (DIDS, 0.5-1.0 mM). 6. Removal of external Cl- and depletion of intracellular Cl- did not inhibit the CO2-HCO3- -dependent alkalinization. 7. The CO2-HCO3- -dependent alkalinization was unaffected by inhibitors of the carbonic anhydrase, acetazolamide (0.2 mM) or ethoxzolamide (2 microM). 8. The membrane potential became more negative by 3-20 mV upon addition of CO2-HCO3-. This hyperpolarization was even further enlarged in the presence of Ba2+ (which reduces the K+ permeability) or at increased external K+ concentration (which depolarizes the membrane and brings the membrane potential to the K+ equilibrium potential). The CO2-HCO3- -induced membrane hyperpolarization was inhibited in Na+-free saline and in the presence of DIDS. Ouabain (0.5 mM) sometimes reduced, but never abolished, the hyperpolarization. 9. The stoichiometry of the co-transport is suggested to be 2 HCO3-:1 Na+ with an equilibrium potential of -90 mV calculated for this coupling ratio in the steady state. 10. It is concluded that in the presence of CO2-HCO3- an inwardly directed electrogenic Na+-HCO3- co-transport is stimulated across the glial membrane, which greatly determines the pHi and thereby affects the intracellular buffering power of the glial cells.
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- Aickin C. C. Direct measurement of intracellular pH and buffering power in smooth muscle cells of guinea-pig vas deferens. J Physiol. 1984 Apr;349:571–585. doi: 10.1113/jphysiol.1984.sp015174. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Alpern R. J. Mechanism of basolateral membrane H+/OH-/HCO-3 transport in the rat proximal convoluted tubule. A sodium-coupled electrogenic process. J Gen Physiol. 1985 Nov;86(5):613–636. doi: 10.1085/jgp.86.5.613. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ammann D., Lanter F., Steiner R. A., Schulthess P., Shijo Y., Simon W. Neutral carrier based hydrogen ion selective microelectrode for extra- and intracellular studies. Anal Chem. 1981 Dec;53(14):2267–2269. doi: 10.1021/ac00237a031. [DOI] [PubMed] [Google Scholar]
- Aronson P. S. Kinetic properties of the plasma membrane Na+-H+ exchanger. Annu Rev Physiol. 1985;47:545–560. doi: 10.1146/annurev.ph.47.030185.002553. [DOI] [PubMed] [Google Scholar]
- Astion M. L., Coles J. A., Orkand R. K. Effects of bicarbonate on glial cell membrane potential in Necturus optic nerve. Neurosci Lett. 1987 Apr 23;76(1):47–52. doi: 10.1016/0304-3940(87)90190-x. [DOI] [PubMed] [Google Scholar]
- Bentley P. J. Amiloride: a potent inhibitor of sodium transport across the toad bladder. J Physiol. 1968 Mar;195(2):317–330. doi: 10.1113/jphysiol.1968.sp008460. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boron W. F., Boulpaep E. L. Intracellular pH regulation in the renal proximal tubule of the salamander. Basolateral HCO3- transport. J Gen Physiol. 1983 Jan;81(1):53–94. doi: 10.1085/jgp.81.1.53. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chesler M., Kraig R. P. Intracellular pH of astrocytes increases rapidly with cortical stimulation. Am J Physiol. 1987 Oct;253(4 Pt 2):R666–R670. doi: 10.1152/ajpregu.1987.253.4.R666. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Curci S., Debellis L., Frömter E. Evidence for rheogenic sodium bicarbonate cotransport in the basolateral membrane of oxyntic cells of frog gastric fundus. Pflugers Arch. 1987 May;408(5):497–504. doi: 10.1007/BF00585075. [DOI] [PubMed] [Google Scholar]
- Deitmer J. W., Schlue W. R. Intracellular Na+ and Ca2+ in leech Retzius neurones during inhibition of the Na+-K+ pump. Pflugers Arch. 1983 May;397(3):195–201. doi: 10.1007/BF00584357. [DOI] [PubMed] [Google Scholar]
- Deitmer J. W., Schlue W. R. The regulation of intracellular pH by identified glial cells and neurones in the central nervous system of the leech. J Physiol. 1987 Jul;388:261–283. doi: 10.1113/jphysiol.1987.sp016614. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Frelin C., Vigne P., Barbry P., Lazdunski M. Molecular properties of amiloride action and of its Na+ transporting targets. Kidney Int. 1987 Dec;32(6):785–793. doi: 10.1038/ki.1987.277. [DOI] [PubMed] [Google Scholar]
- Grinstein S., Rothstein A. Mechanisms of regulation of the Na+/H+ exchanger. J Membr Biol. 1986;90(1):1–12. doi: 10.1007/BF01869680. [DOI] [PubMed] [Google Scholar]
- Jentsch T. J., Keller S. K., Koch M., Wiederholt M. Evidence for coupled transport of bicarbonate and sodium in cultured bovine corneal endothelial cells. J Membr Biol. 1984;81(3):189–204. doi: 10.1007/BF01868713. [DOI] [PubMed] [Google Scholar]
- Jentsch T. J., Matthes H., Keller S. K., Wiederholt M. Electrical properties of sodium bicarbonate symport in kidney epithelial cells (BSC-1). Am J Physiol. 1986 Dec;251(6 Pt 2):F954–F968. doi: 10.1152/ajprenal.1986.251.6.F954. [DOI] [PubMed] [Google Scholar]
- Jentsch T. J., Schill B. S., Schwartz P., Matthes H., Keller S. K., Wiederholt M. Kidney epithelial cells of monkey origin (BSC-1) express a sodium bicarbonate cotransport. Characterization by 22Na+ flux measurements. J Biol Chem. 1985 Dec 15;260(29):15554–15560. [PubMed] [Google Scholar]
- Kettenmann H., Schlue W. R. Intracellular pH regulation in cultured mouse oligodendrocytes. J Physiol. 1988 Dec;406:147–162. doi: 10.1113/jphysiol.1988.sp017373. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Russell J. M., Boron W. F. Role of choloride transport in regulation of intracellular pH. Nature. 1976 Nov 4;264(5581):73–74. doi: 10.1038/264073a0. [DOI] [PubMed] [Google Scholar]
- Schlue W. R., Deitmer J. W. Direct measurement of intracellular pH in identified glial cells and neurones of the leech central nervous system. Can J Physiol Pharmacol. 1987 May;65(5):978–985. doi: 10.1139/y87-155. [DOI] [PubMed] [Google Scholar]
- Schlue W. R., Deitmer J. W. Extracellular potassium in neuropile and nerve cell body region of the leech central nervous system. J Exp Biol. 1980 Aug;87:23–43. doi: 10.1242/jeb.87.1.23. [DOI] [PubMed] [Google Scholar]
- Schlue W. R., Deitmer J. W. Potassium distribution and membrane potential of sensory neurons in the leech nervous system. J Neurophysiol. 1984 Apr;51(4):689–704. doi: 10.1152/jn.1984.51.4.689. [DOI] [PubMed] [Google Scholar]
- Schlue W. R., Schliep A., Walz W. Fluorescence marking of neuropile glial cells in the central nervous system of the leech Hirudo medicinalis. Cell Tissue Res. 1980;209(2):257–269. doi: 10.1007/BF00237630. [DOI] [PubMed] [Google Scholar]
- Schlue W. R., Thomas R. C. A dual mechanism for intracellular pH regulation by leech neurones. J Physiol. 1985 Jul;364:327–338. doi: 10.1113/jphysiol.1985.sp015748. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Soleimani M., Grassi S. M., Aronson P. S. Stoichiometry of Na+-HCO-3 cotransport in basolateral membrane vesicles isolated from rabbit renal cortex. J Clin Invest. 1987 Apr;79(4):1276–1280. doi: 10.1172/JCI112948. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomas R. C. The role of bicarbonate, chloride and sodium ions in the regulation of intracellular pH in snail neurones. J Physiol. 1977 Dec;273(1):317–338. doi: 10.1113/jphysiol.1977.sp012096. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walz W., Schlue W. R. External ions and membrane potential of leech neuropile glial cells. Brain Res. 1982 May 6;239(1):119–138. doi: 10.1016/0006-8993(82)90837-x. [DOI] [PubMed] [Google Scholar]
- Walz W., Wuttke W., Schlue W. R. The Na+-K+ pump in neuropile glial cells of the medicinal leech. Brain Res. 1983 May 9;267(1):93–100. doi: 10.1016/0006-8993(83)91042-9. [DOI] [PubMed] [Google Scholar]
- Yoshitomi K., Burckhardt B. C., Frömter E. Rheogenic sodium-bicarbonate cotransport in the peritubular cell membrane of rat renal proximal tubule. Pflugers Arch. 1985 Dec;405(4):360–366. doi: 10.1007/BF00595689. [DOI] [PubMed] [Google Scholar]