Recovery of nucleotide levels after cell injury
- 1 February 1981
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Biochemistry
- Vol. 59 (2) , 116-121
- https://doi.org/10.1139/o81-017
Abstract
The major pathway of purine catabolism in mouse kidney during ischemia occurs through IMP, inosine, hypoxanthine, and xanthine. Short periods of ischemia (reversible cell injury) allow a rapid return of the energy charge to control values and a rapid return of ATP and GTP to values of 60–70% of control ATP and GTP then slowly return to control levels over the next 24 h. Long periods of ischemia (irreversible cell injury; ischemic times longer than 1 h) allow a gradual return of the energy charge to control levels. ATP, GTP, or total adenine or guanine nucleotides do not return to control levels even after 24 h of reinfusion under these circumstances. We conclude that irreversibly injured kidney cells retain the ability to phosphorylate purine nucleotides, but lose the ability to restore the concentrations of the purine nucleotides to control values.This publication has 4 references indexed in Scilit:
- Ion-exchange separation of nucleic acid constituents by high-performance liquid chromatographyJournal of Chromatography A, 1979
- Liver adenine nucleotide metabolism during hypothermic anoxia and a recovery period in perfusionJournal of Surgical Research, 1977
- Purine and pyrimidine ribonucleotide contents of rat liver and hepatoma 3924A and the effect of ischemiaLife Sciences, 1976
- The Postanoxic Regeneration of 5-Adenine Nucleotides in Rabbit Kidney Tissue during in Vitro PerfusionScandinavian Journal of Clinical and Laboratory Investigation, 1976