Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1967 Jun;103(3):852–862. doi: 10.1042/bj1030852

Metabolic activities of the isolated perfused rat kidney

J M Nishiitsutsuji-Uwo 1, B D Ross 1, H A Krebs 1
PMCID: PMC1270491  PMID: 6049408

Abstract

1. A technique for perfusing the isolated rat kidney is described. It is primarily designed for the study of renal metabolism but is also suitable for studying some aspects of the secretory function; this was normal with respect to minimal glucosuria. The glomerular filtration rate as measured by creatinine clearance was lower than in vivo and slowly decreased with time. 2. Gluconeogenesis from a variety of precursors was rapid and similar to that in kidney-cortex slices, in contrast with liver where the perfused organ is more effective than slices. Whereas the maximal rates of gluconeogenesis from glycerol and pyruvate were similar in liver and kidney, the rates from succinate, malate and fumarate were 14–20 times, and those from glutamate and aspartate about three times, as high in the kidney. 3. The oxygen consumption of the perfused organ was about twice that of cortex slices, presumably because of the secretory work done in the perfused organ but not in slices. 4. The rate of acetoacetate oxidation was about the same in the perfused organ and in slices but, because of the higher rate of oxygen consumption, the percentage contribution of acetoacetate to the fuel of respiration was lower in the perfused organ. The results suggest that acetoacetate can supply energy for the basal requirements and for gluconeogenesis but not for the secretory work. 5. Glutamine was formed at a high rate from glutamate and at a lower rate from aspartate. The high rates indicate that, in the rat, the kidney is a major source of body glutamine.

Full text

PDF
852

Selected References

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

  1. BAUMAN A. W., CLARKSON T. W., MILES E. M. FUNCTIONAL EVALUATION OF ISOLATED PERFUSED RAT KIDNEY. J Appl Physiol. 1963 Nov;18:1239–1246. doi: 10.1152/jappl.1963.18.6.1239. [DOI] [PubMed] [Google Scholar]
  2. Dickens F., Weil-Malherbe H. Metabolism of normal and tumour tissue: A note on the metabolism of medulla of kidney. Biochem J. 1936 Apr;30(4):659–660. doi: 10.1042/bj0300659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. FINGL E. Tubular excretion of creatinine in the rat. Am J Physiol. 1952 May;169(2):357–362. doi: 10.1152/ajplegacy.1952.169.2.357. [DOI] [PubMed] [Google Scholar]
  4. GLASSER L. Renal excretion of creatinine in the rat. Am J Physiol. 1961 Jan;200:167–169. doi: 10.1152/ajplegacy.1961.200.1.167. [DOI] [PubMed] [Google Scholar]
  5. Hems R., Ross B. D., Berry M. N., Krebs H. A. Gluconeogenesis in the perfused rat liver. Biochem J. 1966 Nov;101(2):284–292. doi: 10.1042/bj1010284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Henning H. V., Stumpf B., Ohly B., Seubert W. On the mechanism of gluconeogenesis and its regulation. 3. The glucogenic capacity and the activities of pyruvate carboxylase and PEP-carboxylase of rat kidney and rat liver after cortisol treatment and starvation. Biochem Z. 1966 Apr 27;344(3):274–288. [PubMed] [Google Scholar]
  7. KREBS H. A., BENNETT D. A., DE GASQUET P., GASQUET P., GASCOYNE T., YOSHIDA T. Renal gluconeogenesis. The effect of diet on the gluconeogenic capacity of rat-kidney-cortex slices. Biochem J. 1963 Jan;86:22–27. doi: 10.1042/bj0860022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. KREBS H. A., HEMS R., GASCOYNE T. RENAL GLUCONEOGENESIS. IV. GLUCONEOGENESIS FROM SUBSTRATE COMBINATIONS. Acta Biol Med Ger. 1963;11:607–615. [PubMed] [Google Scholar]
  9. KREBS H. A., SPEAKE R. N., HEMS R. ACCELERATION OF RENAL GLUCONEOGENESIS BY KETONE BODIES AND FATTY ACIDS. Biochem J. 1965 Mar;94:712–720. doi: 10.1042/bj0940712. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Krebs H. A., Gascoyne T., Notton B. M. Generation of extramitochondrial reducing power in gluconeogenesis. Biochem J. 1967 Jan;102(1):275–282. doi: 10.1042/bj1020275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Krebs H. A., Hems R., Weidemann M. J., Speake R. N. The fate of isotopic carbon in kidney cortex synthesizing glucose from lactate. Biochem J. 1966 Oct;101(1):242–249. doi: 10.1042/bj1010242. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Krebs H. A. Metabolism of amino-acids: The synthesis of glutamine from glutamic acid and ammonia, and the enzymic hydrolysis of glutamine in animal tissues. Biochem J. 1935 Aug;29(8):1951–1969. doi: 10.1042/bj0291951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. MILLER L. L., BLY C. G., WATSON M. L., BALE W. F. The dominant role of the liver in plasma protein synthesis; a direct study of the isolated perfused rat liver with the aid of lysine-epsilon-C14. J Exp Med. 1951 Nov;94(5):431–453. doi: 10.1084/jem.94.5.431. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Ross B. D., Hems R., Krebs H. A. The rate of gluconeogenesis from various precursors in the perfused rat liver. Biochem J. 1967 Mar;102(3):942–951. doi: 10.1042/bj1020942. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. SCHIMASSEK H. [Metabolites of carbohydrate metabolism in the isolated perfused rat liver]. Biochem Z. 1963;336:460–467. [PubMed] [Google Scholar]
  16. TOBIAN L., COFFEE K., FERREIRA D., MEULI J. THE EFFECT OF RENAL PERFUSION PRESSURE ON THE NET TRANSPORT OF SODIUM OUT OF DISTAL TUBULAR URINE AS STUDIED WITH THE STOP-FLOW TECHNIQUE. J Clin Invest. 1964 Jan;43:118–128. doi: 10.1172/JCI104886. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. VESTERGAARD P., LEVERETT R. Constancy of urinary creatinine excretion. J Lab Clin Med. 1958 Feb;51(2):211–218. [PubMed] [Google Scholar]
  18. WEISS C., PASSOW H., ROTHSTEIN A. Autoregulation of flow in isolated rat kidney in the absence of red cells. Am J Physiol. 1959 May;196(5):1115–1118. doi: 10.1152/ajplegacy.1959.196.5.1115. [DOI] [PubMed] [Google Scholar]
  19. WU C. GLUTAMINE SYNTHETASE. 3. FACTORS CONTROLLING ITS ACTIVITY IN THE DEVELOPING RAT. Arch Biochem Biophys. 1964 Jul 20;106:394–401. doi: 10.1016/0003-9861(64)90206-1. [DOI] [PubMed] [Google Scholar]
  20. WU C. GLUTAMINE SYNTHETASE. II. THE INTRACELLULAR LOCALIZATION IN THE RAT LIVER. Biochim Biophys Acta. 1963 Nov 8;77:482–493. doi: 10.1016/0006-3002(63)90524-9. [DOI] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES