Skip to main content
The Journal of General Physiology logoLink to The Journal of General Physiology
. 1991 Feb 1;97(2):195–217. doi: 10.1085/jgp.97.2.195

Increased Na/H antiporter and Na/3HCO3 symporter activities in chronic hyperfiltration. A model of cell hypertrophy

PMCID: PMC2216475  PMID: 1849958

Abstract

The effect of chronic hyperfiltration, a model of cell hypertrophy, on H/HCO3 transporters was examined in the in vivo microperfused rat proximal tubule. Hyperfiltration was induced by uninephrectomy with subsequent increased dietary protein. After 2 wk the hyperfiltration group had a higher glomerular filtration rate (2.21 +/- 0.13 vs. 1.48 +/- 0.12 ml/min), associated with increased kidney weight (1.71 +/- 0.05 vs. 1.23 +/- 0.04 g). HCO3 absorptive rate measured in tubules perfused with an ultrafiltrate-like solution (25 mM HCO3) was higher in the hyperfiltration group (183 +/- 17 vs. 109 +/- 16 pmol/mm per min). The activities of the apical membrane Na/H antiporter and basolateral membrane Na/3HCO3 symporter were assayed using the measurement of cell pH [(2'7')-bis(carboxyethyl)-(5,6)-carboxyfluorescein] in the doubly microperfused tubule in the absence of contact with native fluids. After 2 wk of hyperfiltration Na/H antiporter activity, assayed as the effect of luminal Na removal on cell pH, was increased 114%. Basolateral membrane Na/3HCO3 symporter activity, assayed as the effect of a decrease in peritubular [HCO3] (25 to 5 mM) or in peritubular [Na] (147 to 25 mM) in the absence of luminal and peritubular chloride, was increased 77 and 113%, respectively, in the hyperfiltration group. Steady-state cell pH, measured with physiologic, ultrafiltrate-like luminal and peritubular perfusates, was significantly higher in the hyperfiltration group (7.27 +/- 0.02 vs. 7.14 +/- 0.03). In similar studies, performed 24 h after uninephrectomy and protein feeding, kidney weight was increased 10%, Na/H antiporter activity 39%, and Na/3HCO3 symporter activity 46%. At this time cell pH was not different between the two groups. The results demonstrate that chronic hyperfiltration is associated with parallel increases in Na/H antiporter and Na/3HCO3 symporter activities. If a decrease in cell pH is the signal that triggers these adaptations, it occurs early, and the adaptations can be maintained in the absence of sustained cell acidification.

Full Text

The Full Text of this article is available as a PDF (1.6 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Adam W. R., Koretsky A. P., Weiner M. W. 31P-NMR in vivo measurement of renal intracellular pH: effects of acidosis and K+ depletion in rats. Am J Physiol. 1986 Nov;251(5 Pt 2):F904–F910. doi: 10.1152/ajprenal.1986.251.5.F904. [DOI] [PubMed] [Google Scholar]
  2. Akiba T., Rocco V. K., Warnock D. G. Parallel adaptation of the rabbit renal cortical sodium/proton antiporter and sodium/bicarbonate cotransporter in metabolic acidosis and alkalosis. J Clin Invest. 1987 Aug;80(2):308–315. doi: 10.1172/JCI113074. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Alpern R. J. Apical membrane chloride/base exchange in the rat proximal convoluted tubule. J Clin Invest. 1987 Apr;79(4):1026–1030. doi: 10.1172/JCI112914. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Alpern R. J. Cell mechanisms of proximal tubule acidification. Physiol Rev. 1990 Jan;70(1):79–114. doi: 10.1152/physrev.1990.70.1.79. [DOI] [PubMed] [Google Scholar]
  5. Alpern R. J., Chambers M. Cell pH in the rat proximal convoluted tubule. Regulation by luminal and peritubular pH and sodium concentration. J Clin Invest. 1986 Aug;78(2):502–510. doi: 10.1172/JCI112602. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Alpern R. J., Cogan M. G., Rector F. C., Jr Flow dependence of proximal tubular bicarbonate absorption. Am J Physiol. 1983 Oct;245(4):F478–F484. doi: 10.1152/ajprenal.1983.245.4.F478. [DOI] [PubMed] [Google Scholar]
  7. 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]
  8. Aronson P. S., Nee J., Suhm M. A. Modifier role of internal H+ in activating the Na+-H+ exchanger in renal microvillus membrane vesicles. Nature. 1982 Sep 9;299(5879):161–163. doi: 10.1038/299161a0. [DOI] [PubMed] [Google Scholar]
  9. Bank N., Su W. S., Aynedjian H. S. A micropuncture study of HCO3 reabsorption by the hypertrophied proximal tubule. Yale J Biol Med. 1978 May-Jun;51(3):275–282. [PMC free article] [PubMed] [Google Scholar]
  10. Barfuss D. W., Schafer J. A. Flow dependence of nonelectrolyte absorption in the nephron. Am J Physiol. 1979 Feb;236(2):F163–F174. doi: 10.1152/ajprenal.1979.236.2.F163. [DOI] [PubMed] [Google Scholar]
  11. Beer D. G., Zweifel K. A., Simpson D. P., Pitot H. C. Specific gene expression during compensatory renal hypertrophy in the rat. J Cell Physiol. 1987 Apr;131(1):29–35. doi: 10.1002/jcp.1041310106. [DOI] [PubMed] [Google Scholar]
  12. Brenner B. M. Nephron adaptation to renal injury or ablation. Am J Physiol. 1985 Sep;249(3 Pt 2):F324–F337. doi: 10.1152/ajprenal.1985.249.3.F324. [DOI] [PubMed] [Google Scholar]
  13. Chan Y. L., Biagi B., Giebisch G. Control mechanisms of bicarbonate transport across the rat proximal convoluted tubule. Am J Physiol. 1982 May;242(5):F532–F543. doi: 10.1152/ajprenal.1982.242.5.F532. [DOI] [PubMed] [Google Scholar]
  14. Cogan M. G. Chronic hypercapnia stimulates proximal bicarbonate reabsorption in the rat. J Clin Invest. 1984 Dec;74(6):1942–1947. doi: 10.1172/JCI111614. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Cohn D. E., Hruska K. A., Klahr S., Hammerman M. R. Increased Na+-H+ exchange in brush border vesicles from dogs with renal failure. Am J Physiol. 1982 Sep;243(3):F293–F299. doi: 10.1152/ajprenal.1982.243.3.F293. [DOI] [PubMed] [Google Scholar]
  16. Cohn D. E., Klahr S., Hammerman M. R. Metabolic acidosis and parathyroidectomy increase Na+-H+ exchange in brush border vesicles. Am J Physiol. 1983 Aug;245(2):F217–F222. doi: 10.1152/ajprenal.1983.245.2.F217. [DOI] [PubMed] [Google Scholar]
  17. Fine L. G., Badie-Dezfooly B., Lowe A. G., Hamzeh A., Wells J., Salehmoghaddam S. Stimulation of Na+/H+ antiport is an early event in hypertrophy of renal proximal tubular cells. Proc Natl Acad Sci U S A. 1985 Mar;82(6):1736–1740. doi: 10.1073/pnas.82.6.1736. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Fine L. G., Trizna W., Bourgoignie J. J., Bricker N. S. Functional profile of the isolated uremic nephron. Role of compensatory hypertrophy in the control of fluid reabsorption by the proximal straight tubule. J Clin Invest. 1978 Jun;61(6):1508–1518. doi: 10.1172/JCI109071. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Fine L. The biology of renal hypertrophy. Kidney Int. 1986 Mar;29(3):619–634. doi: 10.1038/ki.1986.45. [DOI] [PubMed] [Google Scholar]
  20. Ganz M. B., Boyarsky G., Sterzel R. B., Boron W. F. Arginine vasopressin enhances pHi regulation in the presence of HCO3- by stimulating three acid-base transport systems. Nature. 1989 Feb 16;337(6208):648–651. doi: 10.1038/337648a0. [DOI] [PubMed] [Google Scholar]
  21. Green R., Moriarty R. J., Giebisch G. Ionic requirements of proximal tubular fluid reabsorption flow dependence of fluid transport. Kidney Int. 1981 Nov;20(5):580–587. doi: 10.1038/ki.1981.180. [DOI] [PubMed] [Google Scholar]
  22. 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]
  23. Haggerty J. G., Agarwal N., Reilly R. F., Adelberg E. A., Slayman C. W. Pharmacologically different Na/H antiporters on the apical and basolateral surfaces of cultured porcine kidney cells (LLC-PK1). Proc Natl Acad Sci U S A. 1988 Sep;85(18):6797–6801. doi: 10.1073/pnas.85.18.6797. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Harris R. C., Brenner B. M., Seifter J. L. Sodium-hydrogen exchange and glucose transport in renal microvillus membrane vesicles from rats with diabetes mellitus. J Clin Invest. 1986 Mar;77(3):724–733. doi: 10.1172/JCI112367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Harris R. C., Seifter J. L., Brenner B. M. Adaptation of Na+-H+ exchange in renal microvillus membrane vesicles. Role of dietary protein and uninephrectomy. J Clin Invest. 1984 Dec;74(6):1979–1987. doi: 10.1172/JCI111619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Hayslett J. P. Functional adaptation to reduction in renal mass. Physiol Rev. 1979 Jan;59(1):137–164. doi: 10.1152/physrev.1979.59.1.137. [DOI] [PubMed] [Google Scholar]
  27. Hayslett J. P., Kashgarian M., Epstein F. H. Functional correlates of compensatory renal hypertrophy. J Clin Invest. 1968 Apr;47(4):774–799. doi: 10.1172/JCI105772. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Jacobsen C., Kragh-Hansen U., Sheikh M. I. Na+-H+ exchange in luminal-membrane vesicles from rabbit proximal convoluted and straight tubules in response to metabolic acidosis. Biochem J. 1986 Oct 15;239(2):411–416. doi: 10.1042/bj2390411. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Johnson H. A., Vera Roman J. M. Compensatory renal enlargement. Hypertrophy versus hyperplasia. Am J Pathol. 1966 Jul;49(1):1–13. [PMC free article] [PubMed] [Google Scholar]
  30. Johnston J. R., Brenner B. M., Hebert S. C. Uninephrectomy and dietary protein affect fluid absorption in rabbit proximal straight tubules. Am J Physiol. 1987 Aug;253(2 Pt 2):F222–F233. doi: 10.1152/ajprenal.1987.253.2.F222. [DOI] [PubMed] [Google Scholar]
  31. Kinsella J., Cujdik T., Sacktor B. Na+-H+ exchange activity in renal brush border membrane vesicles in response to metabolic acidosis: The role of glucocorticoids. Proc Natl Acad Sci U S A. 1984 Jan;81(2):630–634. doi: 10.1073/pnas.81.2.630. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Krapf R. Mechanisms of adaptation to chronic respiratory acidosis in the rabbit proximal tubule. J Clin Invest. 1989 Mar;83(3):890–896. doi: 10.1172/JCI113973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Kunau R. T., Jr, Hart J. I., Walker K. A. Effect of metabolic acidosis on proximal tubular total CO2 absorption. Am J Physiol. 1985 Jul;249(1 Pt 2):F62–F68. doi: 10.1152/ajprenal.1985.249.1.F62. [DOI] [PubMed] [Google Scholar]
  34. Maddox D. A., Horn J. F., Famiano F. C., Gennari F. J. Load dependence of proximal tubular fluid and bicarbonate reabsorption in the remnant kidney of the Munich-Wistar rat. J Clin Invest. 1986 May;77(5):1639–1649. doi: 10.1172/JCI112481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Nord E. P., Hafezi A., Kaunitz J. D., Trizna W., Fine L. G. pH gradient-dependent increased Na+-H+ antiport capacity of the rabbit remnant kidney. Am J Physiol. 1985 Jul;249(1 Pt 2):F90–F98. doi: 10.1152/ajprenal.1985.249.1.F90. [DOI] [PubMed] [Google Scholar]
  36. Norman J. T., Bohman R. E., Fischmann G., Bowen J. W., McDonough A., Slamon D., Fine L. G. Patterns of mRNA expression during early cell growth differ in kidney epithelial cells destined to undergo compensatory hypertrophy versus regenerative hyperplasia. Proc Natl Acad Sci U S A. 1988 Sep;85(18):6768–6772. doi: 10.1073/pnas.85.18.6768. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Preisig P. A., Alpern R. J. Basolateral membrane H-OH-HCO3 transport in the proximal tubule. Am J Physiol. 1989 May;256(5 Pt 2):F751–F765. doi: 10.1152/ajprenal.1989.256.5.F751. [DOI] [PubMed] [Google Scholar]
  38. Preisig P. A., Alpern R. J. Chronic metabolic acidosis causes an adaptation in the apical membrane Na/H antiporter and basolateral membrane Na(HCO3)3 symporter in the rat proximal convoluted tubule. J Clin Invest. 1988 Oct;82(4):1445–1453. doi: 10.1172/JCI113750. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Preisig P. A., Ives H. E., Cragoe E. J., Jr, Alpern R. J., Rector F. C., Jr Role of the Na+/H+ antiporter in rat proximal tubule bicarbonate absorption. J Clin Invest. 1987 Oct;80(4):970–978. doi: 10.1172/JCI113190. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Roos A., Boron W. F. Intracellular pH. Physiol Rev. 1981 Apr;61(2):296–434. doi: 10.1152/physrev.1981.61.2.296. [DOI] [PubMed] [Google Scholar]
  41. Ruiz O. S., Arruda J. A., Talor Z. Na-HCO3 cotransport and Na-H antiporter in chronic respiratory acidosis and alkalosis. Am J Physiol. 1989 Mar;256(3 Pt 2):F414–F420. doi: 10.1152/ajprenal.1989.256.3.F414. [DOI] [PubMed] [Google Scholar]
  42. Soleimani M., Bergman J. A., Hosford M. A., McKinney T. D. Potassium depletion increases luminal Na+/H+ exchange and basolateral Na+:CO3=:HCO3- cotransport in rat renal cortex. J Clin Invest. 1990 Oct;86(4):1076–1083. doi: 10.1172/JCI114810. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Tabei K., Levenson D. J., Brenner B. M. Early enhancement of fluid transport in rabbit proximal straight tubules after loss of contralateral renal excretory function. J Clin Invest. 1983 Sep;72(3):871–881. doi: 10.1172/JCI111058. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Talor Z., Yang W. C., Shuffield J., Sack E., Arruda J. A. Chronic hypercapnia enhances Vmax of Na-H antiporter of renal brush-border membranes. Am J Physiol. 1987 Sep;253(3 Pt 2):F394–F400. doi: 10.1152/ajprenal.1987.253.3.F394. [DOI] [PubMed] [Google Scholar]
  45. Trizna W., Yanagawa N., Bar-Khayim Y., Houston B., Fine L. G. Functional profile of the isolated uremic nephron. Evidence of proximal tubular "memory" in experimental renal disease. J Clin Invest. 1981 Sep;68(3):760–767. doi: 10.1172/JCI110312. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Tsai C. J., Ives H. E., Alpern R. J., Yee V. J., Warnock D. G., Rector F. C., Jr Increased Vmax for Na+/H+ antiporter activity in proximal tubule brush border vesicles from rabbits with metabolic acidosis. Am J Physiol. 1984 Aug;247(2 Pt 2):F339–F343. doi: 10.1152/ajprenal.1984.247.2.F339. [DOI] [PubMed] [Google Scholar]
  47. Weber H., Lin K. Y., Bricker N. S. Effect of sodium intake on single nephron glomerular filtration rate and sodium reabsorption in experimental uremia. Kidney Int. 1975 Jul;8(1):14–20. doi: 10.1038/ki.1975.71. [DOI] [PubMed] [Google Scholar]
  48. Wong N. L., Quamme G. A., Dirks J. H. Tubular handling of bicarbonate in dogs with experimental renal failure. Kidney Int. 1984 Jun;25(6):912–918. doi: 10.1038/ki.1984.109. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of General Physiology are provided here courtesy of The Rockefeller University Press

RESOURCES