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. 1968 Feb;194(3):573–594. doi: 10.1113/jphysiol.1968.sp008426

Factors modifying renal tubular bicarbonate reabsorption in the dog

Elisabeth Ullmann
PMCID: PMC1365654  PMID: 5636989

Abstract

1. Acute experiments were carried out on anaesthetized dogs during metabolic alkalosis produced by I.V. administration of NaHCO3. Partial constriction of one ureter led to a significant rise in the HCO3- threshold, beyond the simultaneous value for the other kidney. The magnitude of the increase was not correlated with the reduction of glomerular filtration.

2. Stop-flow analysis, following complete unilateral obstruction of urine flow, demonstrated proximal as well as distal tubular reabsorption of bicarbonate. At any given plasma Pco2 the detailed configuration of the concentration changes which developed depended on (a) the presence and concentration of mannitol, (b) the duration of urinary stasis, and (c) the plasma concentration of HCO3-.

3. If a solution containing 15% (w/v) mannitol was infused I.V., the HCO3- concentration in free flow urine was lower than in plasma, and it fell further during arrest of flow in the entire column of trapped fluid. If less mannitol was infused, or none at all, interruption of urine flow led to a striking increase of HCO3- concentration in the distal portion of the occluded column, and to a fall in the fluid arrested in the proximal segments.

4. It was demonstrated that the HCO3- concentration attained after 2½, 6, or 15 min of urinary stasis at any point in the trapped fluid column was due to the combined effects of water reabsorption and HCO3- reabsorption which proceeded independently, and with a different time course.

5. If mannitol was administered the lowest urinary HCO3- concentration in the series moved progressively to a more distal location with increasing duration of urinary stasis. When HCO3- concentration peaks were present in distal fluid they were conspicuous only after short interruptions of urine flow; during extended stop-flow periods they became attenuated, or disappeared. If no mannitol was administered this did not occur.

6. Provided the plasma level of HCO3- was sufficiently elevated, mannitol (15%, w/v) was administered, and the time available for reabsorption was lengthened by ureter obstruction, much larger concentration differences between plasma and trapped fluid developed than the largest that are ever found between the plasma and freely draining urine. The magnitude of the largest plasma—urine (P—U) concentration difference for HCO3- increased with intratubular `contact time', and no limiting value was found.

7. Potassium concentration in distal occluded fluid fell with prolonged duration of stasis. This was related to the slow and progressive diminution of distal HCO3- concentration. But if instead of bicarbonate a nonreabsorbable anion, such as phosphate, was the dominant distal anion, K+ concentration in distal fractions remained high and rose further with time.

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Selected References

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

  1. CLAPP J. R., WATSON J. F., BERLINER R. W. OSMOLALITY, BICARBONATE CONCENTRATION, AND WATER REABSORPTION IN PROXIMAL TUBULE OF THE DOG NEPHRON. Am J Physiol. 1963 Aug;205:273–280. doi: 10.1152/ajplegacy.1963.205.2.273. [DOI] [PubMed] [Google Scholar]
  2. Eggleton M. G. Urine acidity in alcohol diuresis in man. J Physiol. 1946 Jan 15;104(3):312–320. doi: 10.1113/jphysiol.1946.sp004124. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. GOTTSCHALK C. W., LASSITER W. E., MYLLE M. Localization of urine acidification in the mammalian kidney. Am J Physiol. 1960 Mar;198:581–585. doi: 10.1152/ajplegacy.1960.198.3.581. [DOI] [PubMed] [Google Scholar]
  4. HOAGLAND H. C., SOLOMON S. Stop-flow studies of alkaline urines. Experientia. 1962 May 15;18:228–229. doi: 10.1007/BF02148315. [DOI] [PubMed] [Google Scholar]
  5. LITCHFIELD J. B., BOTT P. A. Micropuncture study of renal excretion of water, K, Na, and Cl in the rat. Am J Physiol. 1962 Oct;203:667–670. doi: 10.1152/ajplegacy.1962.203.4.667. [DOI] [PubMed] [Google Scholar]
  6. MALVIN R. L., WILDE W. S., SULLIVAN L. P. Bicarbonate reabsorption along renal tubules. Proc Soc Exp Biol Med. 1958 Jun;98(2):448–450. doi: 10.3181/00379727-98-24072. [DOI] [PubMed] [Google Scholar]
  7. METAXAS P., BILLIS A., BULL G. M. A study of individual tubular transport systems using the ischaemic stop-flow techniques. Clin Sci. 1963 Apr;24:259–273. [PubMed] [Google Scholar]
  8. MOREL F., MYLLE M., GOTTSCHALK C. W. TRACER MICROINJECTION STUDIES OF EFFECT OF ADH ON RENAL TUBULAR DIFFUSION OF WATER. Am J Physiol. 1965 Jul;209:179–187. doi: 10.1152/ajplegacy.1965.209.1.179. [DOI] [PubMed] [Google Scholar]
  9. NUTBOURNE D. M., DE WARDENER H. E. The effect of a water diuresis on the urinary excretion hydrogen ions in man. Clin Sci. 1961 Feb;20:63–73. [PubMed] [Google Scholar]
  10. PITTS R. F., GURD R. S., KESSLER R. H., HIERHOLZER K. Localization of acidification of urine, potassium and ammonia secretion and phosphate reabsorption in the nephron of the dog. Am J Physiol. 1958 Jul;194(1):125–134. doi: 10.1152/ajplegacy.1958.194.1.125. [DOI] [PubMed] [Google Scholar]
  11. RECTOR F. C., Jr, CARTER N. W., SELDIN D. W. THE MECHANISM OF BICARBONATE REABSORPTION IN THE PROXIMAL AND DISTAL TUBULES OF THE KIDNEY. J Clin Invest. 1965 Feb;44:278–290. doi: 10.1172/JCI105142. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. RECTOR F. C., Jr, SELDIN D. W., ROBERTS A. D., Jr, SMITH J. S. The role of plasma CO2 tension and carbonic anhydrase activity in the renal reabsorption of bicarbonate. J Clin Invest. 1960 Nov;39:1706–1721. doi: 10.1172/JCI104193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. REID E. L., HILLS A. G. DIFFUSION OF CARBON DIOXIDE OUT OF THE DISTAL NEPHRON IN MAN DURING ANTIDIURESIS. Clin Sci. 1965 Feb;28:15–28. [PubMed] [Google Scholar]
  14. SCHREINER G. E. Determination of inulin by means of resorcinol. Proc Soc Exp Biol Med. 1950 May;74(1):117–120. doi: 10.3181/00379727-74-17827. [DOI] [PubMed] [Google Scholar]
  15. Smith H. W., Finkelstein N., Aliminosa L., Crawford B., Graber M. THE RENAL CLEARANCES OF SUBSTITUTED HIPPURIC ACID DERIVATIVES AND OTHER AROMATIC ACIDS IN DOG AND MAN. J Clin Invest. 1945 May;24(3):388–404. doi: 10.1172/JCI101618. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. TAYLOR M. G., ULLMANN E. Glomerular filtration after obstruction of the ureter. J Physiol. 1961 Jun;157:38–63. doi: 10.1113/jphysiol.1961.sp006704. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. THOMPSON D. D., BARRETT M. J. Renal reabsorption of bicarbonate. Am J Physiol. 1954 Feb;176(2):201–206. doi: 10.1152/ajplegacy.1954.176.2.201. [DOI] [PubMed] [Google Scholar]
  18. VANDER A. J. Potassium secretion and reabsorption in distal nephron. Am J Physiol. 1961 Sep;201:505–510. doi: 10.1152/ajplegacy.1961.201.3.505. [DOI] [PubMed] [Google Scholar]
  19. WESSON L. G., Jr Renal function and the velocity effect. J Appl Physiol. 1954 May;6(11):727–730. doi: 10.1152/jappl.1954.6.11.727. [DOI] [PubMed] [Google Scholar]
  20. WILDE W. S., MALVIN R. L. Graphical placement of transport segments along the nephron from urine concentration pattern developed with stop flow technique. Am J Physiol. 1958 Oct;195(1):123–160. doi: 10.1152/ajplegacy.1958.195.1.153. [DOI] [PubMed] [Google Scholar]
  21. Walser M. Mathematical aspects of renal function: the dependence of solute reabsorption on water reabsorption, and the mechanism of osmotic natriuresis. J Theor Biol. 1966 Feb;10(2):307–326. doi: 10.1016/0022-5193(66)90129-9. [DOI] [PubMed] [Google Scholar]

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