Skip to main content
Log in

Evidence for an amiloride sensitive Na+ pathway in the amphibian diluting segment induced by K+ adaptation

  • Transport Processes, Metabolism and Endocrinology; Kidney, Gastrointestinal Tract, and Exocrine Glands
  • Published:
Pflügers Archiv Aims and scope Submit manuscript

Abstract

The effect of amiloride on cell membrane potentials and intracellular Na activity (Nai) was tested in early distal tubules of the isolated perfused kidney of control and of K-adapted (high-K diet)Amphiuma. Conventional and Na-sensitive liquid ion-exchanger microelectrodes were employed to measure the peritubular cell membrane potential (PDpt), the transepithelial potential difference (PDte) and the Na electrochemical gradient across the peritubular cell membrane (E Napt ), in the absence and the presence of amiloride (1·10−4mol·1−1) in both groups of animals. Amiloride did not affect PDpt and E Napt in control animals but depolarized PDpt and E Napt by about 8 mV in K-adapted animals. Nai (11.0 ±0.6 mmol·l−1 in early distal cells of control animals) did not change significantly by this maneuver. However, Nai decreased to extremely low values (2.3±0.2 mmol·l−1) when the luminal cotransport system for Na, Cl and K was inhibited by the luminal application of furosemide (5·10−5 mol/l) and when the luminal cell membrane was exposed simultaneously to amiloride. The amiloride-induced effects on PDpt, E Napt and Nai occurred within seconds and were fully reversible.

We conclude that high-K diet (K adaptation) induces an amiloride-sensitive pathway in the luminal cell membrane of early distal cells ofAmphiuma which exists in parallel with the furosemide-sensitive cotransport system located in this cell barrier. The results suggest a luminal amiloride-sensitive Na/H exchange mechanism which regulates the luminal K permeability.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Aickin CC, Thomas RC (1977) An investigation of the ionic mechanism of intracellular pH regulation in mouse soleus muscle fibers. J Physiol 273: 295–316

    Google Scholar 

  2. Benos DJ (1982) Amiloride: a molecular probe of sodium transport in tissues and cells. Am J Physiol 242: C131-C145

    Google Scholar 

  3. Boron WF, Boulpaep EL (1983) Intracellular pH regulation in the renal proximal tubule of the salamander: Na−H exchange. J Gen Physiol 81: 29–52

    Google Scholar 

  4. Burg MB, Green N (1973) Function of the thick ascending limb of Henle's loop. Am J Physiol 224: 659–668

    Google Scholar 

  5. Cohen B, Giebisch G, Hansen LL, Teuscher U, Wiederholt M (1983) Relationship between peritubular membrane potential and net fluid reabsorption in the distal renal tubule ofAmphiuma. J Physiol (submitted)

  6. Crabbé J (1972) The mechanism of action of aldosteron. From: Receptors and mechanism of action of steroid hormones, part II, 10: 513–568

  7. Cuthbert AW, Shum WK (1976) Induction of transporting sites in a sodium transporting epithelium. J Physiol 260: 213–235

    Google Scholar 

  8. Davis CW, Finn AL (1982) Sodium transport inhibition by amiloride reduces basolateral membrane potassium conductance in tight epithelia. Science 216: 525–527

    Google Scholar 

  9. Doucet A, Katz AI (1980) Renal potassium adaptation: Na−K-ATPase activity along the nephron after chronic potassium loading. Am J Physiol 238: F380-F386

    Google Scholar 

  10. Ericson AC, Spring KR (1982) Volume regulation by Necturus gallbladder: apical Na+−H+ and Cl−HCO 3 exchange. Am J Physiol. Am J Physiol 243: C146-C150

    Google Scholar 

  11. Friedman PA, Andreoli TE (1982) CO2-stimulated NaCl absorption in the mouse renal cortical thick ascending limb of Henle. Evidence for synchronous Na+/H+ and Cl/HCO 3 exchange in apical plasma membranes. J Gen Physiol 80: 683–711

    Google Scholar 

  12. Frizzell RA, Schultz SG (1978) Effect of aldosterone on ion transport by rabbit colon in vitro. J Membr Biol 39: 1–26

    Google Scholar 

  13. Fromm M, Hegel U (1978) Segmental heterogeneity of epithelial transport in rat large intestine. Pflügers Arch 378: 71–83

    Google Scholar 

  14. Giebisch F (1979) Renal potassium transport. In: Giebisch G, Tosteson D, Ussing HH (eds) Transport across biological membranes. Springer, Berlin Heidelberg New York

    Google Scholar 

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

    Google Scholar 

  16. Greger R, Schlatter E, Lang F (1983) Evidence for electroneutral chloride cotransport in the cortical thick ascending limb of Henle's loop for rabbit kidney. Pflügers Arch 396: 308–314

    Google Scholar 

  17. Greger R, Schlatter E (1983a) Properties of the lumen membrane of the cortical thick ascending limb of Henle's loop of rabbit kidney. Pflügers Arch 396: 325–334

    Google Scholar 

  18. Greger R, Schlatter E (1983b) Properties of the basolateral membrane of the cortical thick ascending of Henle's loop of rabbit kidney. A model for secondary active chloride transport. Pflügers Arch 396: 315–324

    Google Scholar 

  19. Guggino WB, Oberleithner H, Giebisch G (1982) Relationship between cell volume and ion transport in the diluting segment of Amphiuma kidney. 15th Ann Meeting, Am Soc Nephrol, Chicago, A163

  20. Hansen L, Teuscher U, Giebisch G, Wiederholt M (1975) Influence of luminally administered amiloride, ouabain, and amphotericin B on peritubular membrane potential and net volume reabsorption in the distal tubule. Pflügers Arch 359: R123

    Google Scholar 

  21. Kaissling B, Le Hir M (1982) Distal tubular segments of the rabbit kidney after adaptation to altered Na- and K-intake. I. Structural changes. Cell Tissue Res 224: 469–492

    Google Scholar 

  22. Katz AI (1982) Renal Na−K-ATPase: its role in tubular sodium and potassium transport. Am J Physiol 242: F207-F219

    Google Scholar 

  23. Kinsella JL, Aronson PS (1981) Amiloride inhibition of the Na+−H+ exchanger in renal microvillus membrane vesicles. Am J Physiol 241: F374-F379

    Google Scholar 

  24. Kregenow FM (1981) Osmoregulatory salt transporting mechanisms: Control of cell volume in anisotonic media. Ann Rev Physiol 43: 493–505

    Google Scholar 

  25. Le Hir M, Kaissling B, Dubach UC (1982) Distal tubular segments of the rabbit kidney after adaptation to altered Na- and K-intake. II. Changes in Na−K-ATPase activity. Cell Tissue Res 224: 493–504

    Google Scholar 

  26. Ludens JH, Fanestil DD (1974) Aldosteron stimulation of acidification of urine by isolated urinary bladder of the Colombian toad. Am J Physiol 226: 1321–1326

    Google Scholar 

  27. Marver D, Kokko JP (1983) Renal target sites and the mechanism of action of aldosterone. Mineral Electrolyte Metab 9: 1–18

    Google Scholar 

  28. Nagel W, Crabbé J (1980) Mechanism of action of aldosterone on active sodium transport across toad skin. Pflügers Arch 385: 181–187

    Google Scholar 

  29. Oberleithner H, Guggino W, Giebisch G (1981) The cellular mechanism of potassium adaptation in the distal amphibian nephron. J Physiol 318: 55p

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

    Google Scholar 

  31. Oberleithner H, Guggino W, Giebisch G (1983) Potassium transport in the early distal tubule of kidney. Effects of potassium adaptation. Pflügers Arch 396: 185–191

    Google Scholar 

  32. Oberleithner H, Lang F, Wang W, Deetjen P (1982) Potassium (K+)-adaptation affects chloride (Cl) reabsorption in the diluting segment ofAmphiuma. Nieren- und Hochdruckkrankheiten 5: 180

    Google Scholar 

  33. Oberleithner H, Lang F, Wang W, Giebisch G, (1982) Effect of inhibition of chloride transport on intracellular sodium activity in distal amphibian nephron. Pflügers Arch 394: 55–60

    Google Scholar 

  34. Oberleithner H, Lang F, Wang W, Messner G (1983) Evidence for stimulation of Na/H-exchange by K-adaptation in frog diluting segment. 16th Ann Meeting, Am Soc Nephrol, Washington, (in press)

  35. Oberleithner H, Guggino W, Giebisch G (1983) The effect of furosemide on luminal sodium, chloride and potassium transport in the early distal tubule ofAmphiuma kidney. Effects of potassium adaptation. Pflügers Arch 396: 27–33

    Google Scholar 

  36. Oberleithner H, Lang F, Greger R, Wang W, Giebisch G (1983) Effect of luminal potassium on cellular sodium activity in the early distal tubule ofAmphiuma kidney. Pflügers Arch 396: 34–40

    Google Scholar 

  37. Oberleithner H, Ritter M, Lang F, Guggino W (1983) Anthracene-9-carboxylic acid inhibits renal chloride reabsorption. Pflügers Arch 398: 172–174

    Google Scholar 

  38. Petty KJ, Kokko JP, Marver DC (1981) Effects of amiloride on the acute rise in aldosterone-dependent Na−K-ATPase activity in single isolated rabbit cortical collecting tubule. Abstracts Int Congr Nephrology, Athens, TT-073

  39. Pfaller W, Fischer WM, Strieder N, Wurnig H, Deetjen P (1974) Morphologic changes of cortical nephron cells in potassium-adapted rats. Lab Invest 31: 678–684

    Google Scholar 

  40. Schwartz GJ (1981) Na+-dependent H+ efflux from proximal tubule: evidence for reversible Na+−H+ exchange. Am J Physiol 241: F380-F385

    Google Scholar 

  41. Stanton B, Biemesderfer D, Wade J, Giebisch G (1981) Structural and functional study of the rat distal nephron: effect of potassium adaptation and depletion. Kidney Int 19: 36–48

    Google Scholar 

  42. Stanton BA, Giebisch GH (1982) Potassium transport by the renal distal tubule: effects of potassium loading. Am J Physiol 243: F487-F493

    Google Scholar 

  43. 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 

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

    Google Scholar 

  45. Ullrich KJ, Cassola AC, Papavassiliou F, Frömter E, Hopfer U (1982) Induction of amiloride-sensitive Na+-transport on the proximal convolution of the rat kidney by low Na+ diet and aldosterone. IVth Europ Coll Renal Physiol, Prague, p 127

  46. Vetter W, Vetter H, Siegenthaler W (1973) Radioimmunoassay for aldosterone without chromatography. 2. Determination of plasma aldosterone. Acta Endocrinol 74: 558

    Google Scholar 

  47. Weinman SA, Reuss L (1982) Na+−H+ exchange at the apical membrane of Necturus gallbladder. J Gen Physiol 80: 299–321

    Google Scholar 

  48. Wiederholt M, Hansen LL (1980)Amphiuma kidney as a model for distal tubular transport studies. Contr Nephrol 19: 28–32

    Google Scholar 

  49. Wiederholt M, Sullivan WH, Giebisch G (1971) Potassium and sodium transport across single distal tubules ofAmphiuma. J Gen Physiol 57: 495–525

    Google Scholar 

  50. Will PC, Lebowitz JL, Hopfer U (1980) Induction of amiloride-sensitive sodium transport in the rat colon by mineralocorticoids. Am J Physiol 238: F261-F268

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This work was supported by Österr. Forschungsrat, Proj. No.:4366

Rights and permissions

Reprints and permissions

About this article

Cite this article

Oberleithner, H., Lang, F., Wang, W. et al. Evidence for an amiloride sensitive Na+ pathway in the amphibian diluting segment induced by K+ adaptation. Pflugers Arch. 399, 166–172 (1983). https://doi.org/10.1007/BF00656710

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00656710

Key words

Navigation