Skip to main content
The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 1974 Jan;53(1):117–121. doi: 10.1172/JCI107528

Regulation of Renal Cortex Ammoniagenesis I. STIMULATION OF RENAL CORTEX AMMONIAGENESIS IN VITRO BY PLASMA ISOLATED FROM ACUTELY ACIDOTIC RATS

George A O Alleyne 1, Anne Roobol 1
PMCID: PMC301445  PMID: 4808633

Abstract

We studied the acute renal metabolic response in rats made acidotic by a single oral dose of ammonium chloride. Cortical slices from acutely (2-h) acidotic rats utilized more glutamine and produced more ammonia and glucose from glutamine than slices from normal animals. When cortical slices from normal rats were pretreated in vitro with plasma isolated from acutely acidotic rats, they achieved similar increases in glutamine utilization, ammonia formation, and gluconeogenesis from glutamine. We did not observe such stimulation in normal cortical slices pretreated in a low pH-low bicarbonate medium. Our data show that a nondialysable factor is present in plasma from acutely acidotic rats that may be responsible for the early increase in the urinary ammonia observed in such animals.

Full text

PDF
121

Selected References

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

  1. Alleyne G. A. Renal metabolic response to acid-base changes. II. The early effects of metabolic acidosis on renal metabolism in the rat. J Clin Invest. 1970 May;49(5):943–951. doi: 10.1172/JCI106314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Alleyne G. A., Scullard G. H. Renal metabolic response to acid base changes. I. Enzymatic control of ammoniagenesis in the rat. J Clin Invest. 1969 Feb;48(2):364–370. doi: 10.1172/JCI105993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. DAVIES B. M. A., YUDKIN J. Studies in biochemical adaptation; the origin or urinary ammonia as indicated by the effect of chronic acidosis and alkalosis on some renal enzymes in the rat. Biochem J. 1952 Nov;52(3):407–412. doi: 10.1042/bj0520407. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. HUGGETT A. S., NIXON D. A. Use of glucose oxidase, peroxidase, and O-dianisidine in determination of blood and urinary glucose. Lancet. 1957 Aug 24;273(6991):368–370. doi: 10.1016/s0140-6736(57)92595-3. [DOI] [PubMed] [Google Scholar]
  5. Pagliara A. S., Goodman A. D. Relation of renal cortical gluconeogenesis, glutamate content, and production of ammonia. J Clin Invest. 1970 Nov;49(11):1967–1974. doi: 10.1172/JCI106416. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Pitts R. F. Symposium on acid-base homeostasis. Control of renal production of ammonia. Kidney Int. 1972 May;1(5):297–305. doi: 10.1038/ki.1972.42. [DOI] [PubMed] [Google Scholar]
  7. Simpson D. P., Sherrard D. J. Regulation of glutamine metabolism in vitro by bicarbonate ion and pH. J Clin Invest. 1969 Jun;48(6):1088–1096. doi: 10.1172/JCI106065. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Clinical Investigation are provided here courtesy of American Society for Clinical Investigation

RESOURCES