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. 1966 May 1;123(5):829–844. doi: 10.1084/jem.123.5.829

THE FUNCTIONAL CAPACITY OF HYPERTROPHIED NEPHRONS

EFFECT OF PARTIAL NEPHRECTOMY ON THE CLEARANCE OF INULIN AND PAH IN THE RAT

Ashton B Morrison 1, Ruth M Howard 1
PMCID: PMC2138171  PMID: 5938815

Abstract

A method is described for the measurement of inulin and PAH clearances in rats without killing the animal. Inulin clearance measurements of partially nephrectomized rats and sham-control rats were made before operation and at intervals following the operation; inulin clearances were determined on normal rats at intervals during their growth. In another series of partially nephrectomized rats and their sham-operated controls, inulin and PAH clearances were determined in all the animals before and at intervals following the operation. Glomerular counts were made in some rats. After partial nephrectomy the inulin clearance is reduced but not as much as would be expected considering the amount of renal tissue removed. The mean inulin clearance per nephron is greatly increased in the partially nephrectomized rat when compared to the value determined for the control rat. The inulin clearance of the partially nephrectomized rat shows a progressive decline which is first clearly evident about 6 months after operation. The sham-operated rats showed an inulin clearance slightly less than that of nonoperated controls about 24 to 30 wk after the operation. In the normal rats the inulin clearance relative to body weight is much greater in rats with a mean weight of 197 ± 3 g than in normals which are older and heavier. The PAH dearance of the partially nephrectomized rat is reduced following operation but undergoes no further change in the ensuing 24 wk.

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Selected References

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

  1. BRADLEY S. E., BRADLEY G. P., TYSON C. J., CURRY J. J., BLAKE W. D. Renal function in renal diseases. Am J Med. 1950 Dec;9(6):766–798. doi: 10.1016/0002-9343(50)90292-0. [DOI] [PubMed] [Google Scholar]
  2. BRICKER N. S., MORRIN P. A., KIME S. W., Jr The pathologic physiology of chronic Bright's disease. An exposition of the "intact nephron hypothesis". Am J Med. 1960 Jan;28:77–98. doi: 10.1016/0002-9343(60)90225-4. [DOI] [PubMed] [Google Scholar]
  3. BULL G. M., METAXAS P. The theory and application or clearance methods for determining renal blood and lymph flow. Clin Sci. 1962 Dec;23:515–523. [PubMed] [Google Scholar]
  4. Bacon J. S., Bell D. J. Fructose and glucose in the blood of the foetal sheep. Biochem J. 1948;42(3):397–405. doi: 10.1042/bj0420397. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Book M. H. The Secreting Area of the Glomerulus. J Anat. 1936 Oct;71(Pt 1):91–97. [PMC free article] [PubMed] [Google Scholar]
  6. Bradford J. R. The results following partial Nephrectomy and the influence of the Kidney on Metabolism. J Physiol. 1899 Feb 27;23(6):415–496. doi: 10.1113/jphysiol.1899.sp000738. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. COBURN J. W., GONICK H. C., RUBINI M. E., KLEEMAN C. R. STUDIES OF EXPERIMENTAL RENAL FAILURE IN DOGS. I. EFFECT OF 5-6 NEPHRECTOMY ON CONCENTRATING AND DILUTING CAPACITY OF RESIDUAL NEPHRONS. J Clin Invest. 1965 Apr;44:603–614. doi: 10.1172/JCI105173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. HANDLEY C. A., SIGAFOOS R. B., LA FORGE M. Proportional changes in renal tubular reabsorption of dextrose and excretion of p-amino-hippurate with changes in glomerular filtration. Am J Physiol. 1949 Oct;159(1):175–180. doi: 10.1152/ajplegacy.1949.159.1.175. [DOI] [PubMed] [Google Scholar]
  9. Hayman J. M., Shumway N. P., Dumke P., Miller M. EXPERIMENTAL HYPOSTHENURIA. J Clin Invest. 1939 Mar;18(2):195–212. doi: 10.1172/JCI101035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. KLEINMAN L. I., RADFORD E. P., Jr, TORELLI G. UREA AND INULIN CLEARANCES IN UNDISTURBED, UNANESTHETIZED RATS. Am J Physiol. 1965 Mar;208:578–584. doi: 10.1152/ajplegacy.1965.208.3.578. [DOI] [PubMed] [Google Scholar]
  11. MORRISON A. B. Experimentally induced chronic renal insufficiency in the rat. Lab Invest. 1962 Apr;11:321–332. [PubMed] [Google Scholar]
  12. Moore R. A., Hellman L. M. THE EFFECT OF UNILATERAL NEPHRECTOMY ON THE SENILE ATROPHY OF THE KIDNEY IN THE WHITE RAT. J Exp Med. 1930 Jan 1;51(1):51–57. doi: 10.1084/jem.51.1.51. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. PLATT R., ROSCOE M. H., SMITH F. W. Experimental renal failure. Clin Sci. 1952 Aug;11(3):217–231. [PubMed] [Google Scholar]
  14. Smith H. W., Chasis H., Goldring W., Ranges H. A. GLOMERULAR DYNAMICS IN THE NORMAL HUMAN KIDNEY. J Clin Invest. 1940 Sep;19(5):751–764. doi: 10.1172/JCI101180. [DOI] [PMC free article] [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]

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