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. 1971 May;50(5):1154–1165. doi: 10.1172/JCI106588

The postobstructive kidney. Observations on nephron function after the relief of 24 hr of ureteral ligation in the dog

D Danny Bercovitch 1,2, Leonard Kasen 1,2, Laurence Blann 1,2, Marvin F Levitt 1,2
PMCID: PMC292039  PMID: 5552413

Abstract

After the relief of 24 hr of complete unilateral ureteral obstruction in the dog, the experimental kidney is characterized by a decrease in filtration rate and an increase in fractional and often absolute excretion of sodium before and after the administration of mannitol. In the hydrated state, the failure to conserve sodium is associated with increases in fractional free water clearance and fractional sodium supply to water-freeing sites signifying that the augmented sodium excretion is derived from a proximal source. In the hydropenic state there is decreased fractional free water reabsorption, and sometimes free water excretion, in the postobstructive kidney. An early plateau in free water reabsorption is associated with an increased fractional excretion of sodium. These findings are attributed to the early development of distal nephron impermeability to water as a result of enhanced distal tubular supply and transport of sodium. There is a decrease in maximal tubular reabsorptive capacity (Tm) of glucose in the post-obstructive kidney which is, however, less marked than the decrease in filtration rate. The fall in filtration rate is to some extent likely due to a dropping out of nephrons from the circulation while the remaining nephrons are hypoperfused. The magnitude of the sodium reabsorptive defect is markedly exaggerated as the concentration of nonreabsorbable solute (mannitol) in the glomerular perfusate is increased. It is concluded that the postobstructive increase in sodium excretion during mannitol administration is in part due to a limit in the capacity to reabsorb sodium against a concentration gradient in the proximal tubule.

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Selected References

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

  1. BERLYNE G. M. Distal tubular function in chronic hydronephrosis. Q J Med. 1961 Oct;30:339–355. [PubMed] [Google Scholar]
  2. BRICKER N. S., DEWEY R. R., LUBOWITZ H., STOKES J., KIRKENSGAARD T. Observations on the concentrating and diluting mechanisms of the diseased kidney. J Clin Invest. 1959 Mar;38(3):516–523. doi: 10.1172/JCI103829. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. BRICKER N. S., KIME S. W., Jr, MORRIN P. A., ORLOWSKI T. The influence of glomerular filtration rate, solute excretion and hydration on the concentrating mechanism of the experimentally diseased kidney in the dog. J Clin Invest. 1960 Jun;39:864–875. doi: 10.1172/JCI104107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. BRICKER N. S., SHWAYRI E. I., REARDAN J. B., KELLOG D., MERRILL J. P., HOLMES J. H. An abnormality in renal function resulting from urinary tract obstruction. Am J Med. 1957 Oct;23(4):554–564. doi: 10.1016/0002-9343(57)90226-7. [DOI] [PubMed] [Google Scholar]
  5. Clapp J. R., Robinson R. R. Osmolality of distal tubular fluid in the dog. J Clin Invest. 1966 Dec;45(12):1847–1853. doi: 10.1172/JCI105488. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. EARLEY L. E. Extreme polyuria in obstructive uropathy; report of a case of water-losing nephritis in an infant, with a discussion of polyuria. N Engl J Med. 1956 Sep 27;255(13):600–605. doi: 10.1056/NEJM195609272551305. [DOI] [PubMed] [Google Scholar]
  7. EARLEY L. E., FRIEDLER R. M. RENAL TUBULAR EFFECTS OF ETHACRYNIC ACID. J Clin Invest. 1964 Jul;43:1495–1506. doi: 10.1172/JCI105026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. EARLEY L. E., KAHN M., ORLOFF J. The effects of infusions of chlorothiazide on urinary dilution and concentration in the dog. J Clin Invest. 1961 May;40:857–866. doi: 10.1172/JCI104320. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. GOLDBERG M., MCCURDY D. K., FOLTZ E. L., BLUEMLE L. W., Jr EFFECTS OF ETHACRYNIC ACID (A NEW SALURETIC AGENT) ON RENAL DILUTING AND CONCENTRATING MECHANISMS: EVIDENCE FOR SITE OF ACTION IN THE LOOP OF HENLE. J Clin Invest. 1964 Feb;43:201–216. doi: 10.1172/JCI104905. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. GOLDSMITH C., BEASLEY H. K., WHALLEY P. J., RECTOR F. C., Jr, SELDIN D. W. The effect of salt deprivation on the urinary concentrating mechanism in the dog. J Clin Invest. 1961 Nov;40:2043–2052. doi: 10.1172/JCI104430. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. GOLDSTEIN M. H., LEVITT M. F., HAUSER A. D., POLIMEROS D. Effect of meralluride on solute and water excretion in hydrated man: comments on site of action. J Clin Invest. 1961 Apr;40:731–742. doi: 10.1172/JCI104307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. GOODMAN B., COHEN J. A., LEVITT M. F., KAHN M. RENAL CONCENTRATION IN THE NORMAL DOG: EFFECT OF AN ACUTE REDUCTION IN SALT EXCRETION. Am J Physiol. 1964 May;206:1123–1130. doi: 10.1152/ajplegacy.1964.206.5.1123. [DOI] [PubMed] [Google Scholar]
  13. GOTTSCHALK C. W., MYLLE M. Micropuncture study of the mammalian urinary concentrating mechanism: evidence for the countercurrent hypothesis. Am J Physiol. 1959 Apr;196(4):927–936. doi: 10.1152/ajplegacy.1959.196.4.927. [DOI] [PubMed] [Google Scholar]
  14. JAENIKE J. R., BRAY G. A. Effects of acute transitory urinary obstruction in the dog. Am J Physiol. 1960 Dec;199:1219–1222. doi: 10.1152/ajplegacy.1960.199.6.1219. [DOI] [PubMed] [Google Scholar]
  15. ORLOFF J., WAGNER H. N., Jr, DAVIDSON D. G. The effect of variations in solute excretion and vasopressin dosage on the excretion of water in the dog. J Clin Invest. 1958 Mar;37(3):458–464. doi: 10.1172/JCI103625. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. PORUSH J. G., GOLDSTEIN M. H., EISNER G. M., LEVITT M. F. Effect of organomercurials on the renal concentrating operation in hydropenic man: comments on site of action. J Clin Invest. 1961 Aug;40:1475–1485. doi: 10.1172/JCI104378. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. ROUSSAK N. J., OLEESKY S. Waterlosing nephritis, a syndrome simulating diabetes insipidus. Q J Med. 1954 Apr;23(90):147–164. [PubMed] [Google Scholar]
  18. STEIN R. M., BERCOVITCH D. D., LEVITT M. F. DUAL EFFECTS OF SALINE LOADING ON RENAL TUBULAR SODIUM REABSORPTION IN THE DOG. Am J Physiol. 1964 Oct;207:826–834. doi: 10.1152/ajplegacy.1964.207.4.826. [DOI] [PubMed] [Google Scholar]
  19. SUKI W., RECTOR F. C., Jr, SELDIN D. W. THE SITE OF ACTION OF FUROSEMIDE AND OTHER SULFONAMIDE DIURETICS IN THE DOG. J Clin Invest. 1965 Sep;44:1458–1469. doi: 10.1172/JCI105252. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Seely J. F., Dirks J. H. Micropuncture study of hypertonic mannitol diuresis in the proximal and distal tubule of the dog kidney. J Clin Invest. 1969 Dec;48(12):2330–2340. doi: 10.1172/JCI106199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Stein R. M., Abramson R. G., Bercovitch D. D., Levitt M. F. Effects of unilateral renal arterial constriction on tubular reabsorption of sodium and water during an osmotic diuresis. J Clin Invest. 1965 Oct;44(10):1720–1729. doi: 10.1172/JCI105279. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Suki W., Eknoyan G., Rector F. C., Jr, Seldin D. W. Patterns of nephron perfusion in acute and chronic hydronephrosis. J Clin Invest. 1966 Jan;45(1):122–131. doi: 10.1172/JCI105316. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. WINBERG J. Renal function in water-losing syndrome due to lower urinary tract obstruction before and after treatment. Acta Paediatr. 1959 Mar;48(2):149–163. doi: 10.1111/j.1651-2227.1959.tb16030.x. [DOI] [PubMed] [Google Scholar]
  24. WITTE M. H., SHORT F. A., HOLLANDER W., Jr MASSIVE POLYURIA AND NATRURESIS FOLLOWING RELIEF OF URINARY TRACT OBSTRUCTION. Am J Med. 1964 Aug;37:320–326. doi: 10.1016/0002-9343(64)90015-4. [DOI] [PubMed] [Google Scholar]

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