Abstract
Clearance studies were performed on 49 split-bladder dogs with a unilateral pyelonephritic or remnant kidney and three patients with unilateral kidney disease to examine the effects of an acute saline load on the diseased kidney (DK) as opposed to a simultaneously studied, contralateral control kidney (CK), which also served to maintain a nonuremic environment.
Before saline loading, base line studies in many of the dogs and the three humans were in agreement with previously published data. However, in dogs with a severe pyelonephritic lesion, a greater difference in DK vs. CK fractional excretion of sodium (FENa) and water was noted, whose magnitude was inversely correlated with the level of glomerular filtration rate (GFR) and maximum urine osmolality of DK compared to CK.
An acute saline load (75 ml/kg) resulted in an inhibition of fractional sodium and water reabsorption in the diseased dog kidney which was disproportionately greater than in the simultaneously studied CK, regardless of the type or severity of the lesion. While mean DK GFR for all dogs increased 15% more than CK GFR, failure of FENa to increase after induction of a disproportionate increase in DK GFR with parathyroid hormone suggested that the saline-induced disproportionate increase in GFR was not solely responsible for the exaggerated inhibition of fractional sodium and water reabsorption in the diseased dog kidney. Studies in the three patients after saline loading (25 ml/kg) revealed a similar disproportionate resetting of glomerulotubular balance.
Thus, regardless of base line function before expansion, the unilaterally diseased kidney of dog and man possesses unique characteristics in the absence of uremia which render it more reactive to the stimuli produced by acute saline loading. This suggests that the intrarenal environment of the kidney with a reduced nephron population may under some circumstances serve as a determinant of its function.
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- BRICKER N. S., KLAHR S., LUBOWITZ H., RIESELBACH R. E. RENAL FUNCTION IN CHRONIC RENAL DISEASE. Medicine (Baltimore) 1965 Jul;44:263–288. doi: 10.1097/00005792-196507000-00001. [DOI] [PubMed] [Google Scholar]
- Barger A. C. Renal hemodynamic factors in congestive heart failure. Ann N Y Acad Sci. 1966 Nov 22;139(2):276–284. doi: 10.1111/j.1749-6632.1966.tb41202.x. [DOI] [PubMed] [Google Scholar]
- Bricker N. S. On the meaning of the intact nephron hypothesis. Am J Med. 1969 Jan;46(1):1–11. doi: 10.1016/0002-9343(69)90053-9. [DOI] [PubMed] [Google Scholar]
- Bricker N. S. The control of sodium excretion with normal and reduced nephron populations. The pre-eminence of third factor. Am J Med. 1967 Sep;43(3):313–321. doi: 10.1016/0002-9343(67)90188-x. [DOI] [PubMed] [Google Scholar]
- DESAUTELS R. E. Hemisection of the bladder for the collection of separate urine samples. Surg Gynecol Obstet. 1957 Dec;105(6):767–768. [PubMed] [Google Scholar]
- Earley L. E., Daugharty T. M. Sodium metabolism. N Engl J Med. 1969 Jul 10;281(2):72–86. doi: 10.1056/NEJM196907102810205. [DOI] [PubMed] [Google Scholar]
- Harrington A. R., Rieselbach R. E. Na conservation in rats with reduced medullary osmotic gradient due to diabetes insipidus. Am J Physiol. 1970 Aug;219(2):384–386. doi: 10.1152/ajplegacy.1970.219.2.384. [DOI] [PubMed] [Google Scholar]
- LIDDLE L., SEEGMILLER J. E., LASTER L. The enzymatic spectrophotometric method for determination of uric acid. J Lab Clin Med. 1959 Dec;54:903–913. [PubMed] [Google Scholar]
- MALVIN R. L., KLEMPNER S. RENAL FUNCTION AS AFFECTED BY INTRA-ARTERIAL INJECTION OF PLASTIC MICROSPHERES. J Lab Clin Med. 1964 Apr;63:551–561. [PubMed] [Google Scholar]
- Martino J. A., Earley L. E. Demonstraton of a role of physical factors as determinants of the natriuretic response to volume expansion. J Clin Invest. 1967 Dec;46(12):1963–1978. doi: 10.1172/JCI105686. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schultze R. G., Shapiro H. S., Bricker N. S. Studies on the control of sodium excretion in experimental uremia. J Clin Invest. 1969 May;48(5):869–877. doi: 10.1172/JCI106045. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Steele T. H., Wen S. F., Evenson M. A., Rieselbach R. E. The contribution of the chronically diseased kidney to magnesium homeostasis in man. J Lab Clin Med. 1968 Mar;71(3):455–463. [PubMed] [Google Scholar]


