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Effects of inhibition of chloride transport on intracellular sodium activity in distal Amphibian nephron

  • Transport Processes, Metabolism and Endocrinology; Kidney, Gastrointestinal Tract, and Exocrine Glands
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Abstract

Previous experiments had demonstrated that cell chloride activities in early distal tubule cells of Amphiuma are above equilibrium distribution. Chloride activities fell sharply towards electrochemical equilibrium following perfusion of the tubular lumen with furosemide or with sodium-free solutions. These results suggested a furosemide-sensitive sodium chloride cotransport system in the luminal cell membrane. The present experiments were carried out to evaluate directly the electrochemical driving forces acting on sodium ions under similar experimental conditions. Intracellular sodium activity measurements were performed in the doublyperfused kidney of Amphiuma by means of single-barreled liquid ion-exchange microelectrodes. Basolateral cell membrane potential and resistance ratio measurements of tubular cell membranes were also carried out under control conditions and after inhibition of chloride transport by luminal application of furosemide (5 · 10−5 mol/l) or by omission of chloride.

Control conditions were characterized by a steep downhill electrochemical gradient for sodium ions from lumen to cell. Inhibition of chloride transport led to a sharp decrease of intracellular sodium activity and to hyperpolarization of the peritubular membrane potential while the resistance ratio of the tubular cell membranes did not change significantly. These results demonstrate the presence of low cellular sodium activities in early distal tubule cells. The sharp decline of cell sodium after furosemide and after luminal chloride removal is consistent with inhibition of a sodium chloride cotransport system and continued peritubular sodium extrusion. The latter can increase the electrochemical gradient of sodium ions beyond that observed under control conditions.

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References

  1. Boulpaep EL (1976) Electrical phenomena in the nephron. Kidney Int 9:88–120

    Google Scholar 

  2. Boulpaep EL, Giebisch G (1978) Electrophysiological measurements on the renal tubule. In: Martinex-Maldonado M (ed) Methods in pharmacology. Vol 4B. Plenum Publ Corp. New York London, pp 165–193

    Google Scholar 

  3. Burg M, Stoner L, Cardinal J, Green N (1973) Furosemide effect on isolated perfused tubules. Am J Physiol 225:119–124

    Google Scholar 

  4. Cemericic D, Giebisch G (1980) Intracellular sodium activity in Necturus kidney proximal tubule. Fed Proc 39:1080

    Google Scholar 

  5. Chipperfield AR (1981) Chloride dependence of furosemide-and phloretin-sensitive passive sodium and potassium fluxes in human red cells. J Physiol 312:435–444

    Google Scholar 

  6. Eveloff J, Silva P, Kinne R (1980) Evidence for a coupled Na/Cl transport in plasma membrane vesicles from the thick ascending limb of Henle's loop. Fed Proc 39:734

    Google Scholar 

  7. Fossat B, Lahlou B (1979) The mechanism of coupled transport of sodium and chloride in isolated urinary bladder of the trout. J Physiol 294:211–222

    Google Scholar 

  8. Frizzell RA, Dugas MC, Schultz SG (1975) Sodium chloride transport by rabbit gallbladder. J Gen Physiol 65:769–795

    Google Scholar 

  9. Frizzell RA, Smith PL, Vosburgh E, Field M (1979) Coupled sodium-chloride influx across brush border of flounder intestine. J Membr Biol 46:27–39

    Google Scholar 

  10. Frömter E (1972) The route of passive ion movement through the epithelium of Necturus gallbladder. J Membr Biol 8:259–301

    Google Scholar 

  11. Fujimoto M (1981) Intracellular ion activity measurements in renal tubular epithelium. Proc 8th Int Congr Nephrol Athens, pp 949–955

  12. Geck P, Pietrzyk C, Burckhardt BC, Pfeiffer B, Heinz E (1980) Electrically silent cotransport of Na+, K+ and Cl in Ehrlich cells. Biochim Biophys Acta 600:432–447

    Google Scholar 

  13. Graf J, Giebisch G (1979) Intracellular sodium activity and sodium transport in Necturus gallbladder epithelium. J Membr Biol 47:327–355

    Google Scholar 

  14. Greger R (1981) Chloride reabsorption in the rabbit cortical thick ascending limb of the loop of Henle — a sodium dependent process. Pflügers Arch 390:38–43

    Google Scholar 

  15. Greger R, Schlatter E (1981) Presence of luminal K+, a prerequisite fo active NaCl transport in the cortical thick ascending limb of Henle's loop of rabbit kidney. Pflügers Arch 392:92–94

    Google Scholar 

  16. Hansen LL, Schilling AR, Wiederholt M (1981) Effect of calcium, furosemide and chlorothiazide on net volume reabsorption an basolateral membrane potential of the distal tubule. Pflügers Arch 389:121–126

    Google Scholar 

  17. Imai M (1977) Effect of bumetanide and furosemide on the thick ascending limb of Henle's loop of rabbits and rats perfused in vitro. Eur. J Pharmacol 41:409–416

    Google Scholar 

  18. Kimura G, Spring KR (1979) Luminal Na+ entry into Necturus proximal tubule cells. Am J Physiol 236:F 295-F 301

    Google Scholar 

  19. Machen TE, McLennan WL (1980) Na+-dependent H+ and Cl transport in in vitro frog gastric mucosa. Am J Physiol 238:G403-G413

    Google Scholar 

  20. Nellans HN, Frizzell RA, Schultz SG (1973) Coupled sodiumchloride influx across the brusch border of rabbit ileum. Am J Physiol 225:467–475

    Google Scholar 

  21. Oberleithner H, Giebisch G (1981) Mechanism of potassium transport across distal tubular epithelium of Amphiuma. In: MacKnight ADC, Leader JP (eds) Epithelial ion and water transport. Raven Press, New York, pp 97–105

    Google Scholar 

  22. Oberleithner H, Guggino W, Giebisch (1981) The cellular mechanism of potassium adaptation in the distal amphibian nephron. Proc Physiol Soc 76P

  23. Oberleithner H, Guggino W, Giebisch G (1982) Mechanism of distal tubular chloride transport in amphiuma kidney. Am J Physiol 242: F331-F339

    Google Scholar 

  24. Oberleithner H, Giebisch G, Lang F, Wang W (1982) Cellular mechanism of the furosemide sensitive transport system in the kidney. Klin Wochenschr (in press)

  25. Palfrey HC, Feit PW, Greengard P (1980) cAMP-stimulated cation cotransport in avian erythrocytes: inhibition by “loop” diuretics. Am J Physiol 238:C139-C148

    Google Scholar 

  26. O'Doherty J, Garcia-Diaz JF, Armstrong WMcD (1979) Sodium-selective liquid ion-exchanger microelectrodes for intracellular measurements. Science 203:1349–1351

    Google Scholar 

  27. Reus L, Finn AL (1975) Electrical properties of the cellular transepithelial pathway in Necturus gallbladder. I. Circuit analysis and steady state effects of mucosal solution ionic substitution. J Membr Biol 25:115–130

    Google Scholar 

  28. Robinson RA, Stokes RH (1970) Electrolytic solutions. 2nd edn Butterworth, London

    Google Scholar 

  29. Rocha AS, Kokko JP (1973) Sodium chloride and water transport in the medullary thick ascending limb of Henle. J Clin Invest 52:612–623

    Google Scholar 

  30. Sackin H, Boron W, Boulpaep EL (1980) Intracellular sodium activity in ambystoma renal proximal tubule. In: 13th Annual Meeting of the Am Soc of Nephrol Abstr 148A, Washington

  31. Sackin H, Morgunov N, Boulpaep E (1981) Intracellular microelectrode measurements in the diluting segment of the amphibian nephron. Fed Proc 40:394

    Google Scholar 

  32. Saier MH (1981) Growth and differentiated properties of a kidney epithelial cell line (MDCK) Am J Physiol 240:C106-C109

    Google Scholar 

  33. Steiner RA, Oehme M, Ammann D, Simon W (1979) Neutral carrier sodium ion-selective microelectrode for intracellular studies. Anal Chem 51:351–353

    Google Scholar 

  34. Stoner LC (1977) Isolated perfused amphibian renal tubules. The diluting segment. Am J Physiol 233:F438-F444

    Google Scholar 

  35. Thomas RC (1974) Intracellular pH of snail neurones measured with a new pH-sensitive glass microelectrode. J Physiol 238:159–180

    Google Scholar 

  36. Velazquez H, Wright FS, Good DW. Luminal influences on potassium secretion: Chloride replacement with sulfate. Am J Physiol (in press)

  37. Walker JL (1971) Ionic specific liquid ion-exchanger microelectrodes. Anal Chem 43:89A-93A

    Google Scholar 

  38. Wiederholt M, Sullivan WJ, Giebisch G (1971) Potassium and sodium transport across single distal tubules of Amphiuma. J Gen Physiol 57:495–525

    Google Scholar 

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This work was supported by NIH Grant PHS AM 17433 and by Österreichischem Forschungs-Proj. No.: 4366.

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Oberleithner, H., Lang, F., Wang, W. et al. Effects of inhibition of chloride transport on intracellular sodium activity in distal Amphibian nephron. Pflugers Arch. 394, 55–60 (1982). https://doi.org/10.1007/BF01108308

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  • DOI: https://doi.org/10.1007/BF01108308

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