Literature DB >> 7237228

Recovery of nucleotide levels after cell injury.

C T Warnick, H M Lazarus.   

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 value 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.

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Year:  1981        PMID: 7237228     DOI: 10.1139/o81-017

Source DB:  PubMed          Journal:  Can J Biochem        ISSN: 0008-4018


  8 in total

1.  Clinical and biochemical assessments of damage due to perinatal asphyxia: a double blind trial of a quantitative method.

Authors:  I Laing; J K Brown; R A Harkness
Journal:  J Clin Pathol       Date:  1988-03       Impact factor: 3.411

2.  Ischemia induces partial loss of surface membrane polarity and accumulation of putative calcium ionophores.

Authors:  B A Molitoris; P D Wilson; R W Schrier; F R Simon
Journal:  J Clin Invest       Date:  1985-12       Impact factor: 14.808

3.  Metabolic and functional consequences of inhibiting adenosine deaminase during renal ischemia in rats.

Authors:  M E Stromski; A van Waarde; M J Avison; G Thulin; K M Gaudio; M Kashgarian; R G Shulman; N J Siegel
Journal:  J Clin Invest       Date:  1988-11       Impact factor: 14.808

4.  Exogenous adenosine triphosphate (ATP) preserves proximal tubule microfilament structure and function in vivo in a maleic acid model of ATP depletion.

Authors:  P S Kellerman
Journal:  J Clin Invest       Date:  1993-10       Impact factor: 14.808

5.  Intrapartum hypoxia: the association between neurological assessment of damage and abnormal excretion of ATP metabolites.

Authors:  R A Harkness; A G Whitelaw; R J Simmonds
Journal:  J Clin Pathol       Date:  1982-09       Impact factor: 3.411

6.  Chemical and functional correlates of postischemic renal ATP levels.

Authors:  M E Stromski; K Cooper; G Thulin; K M Gaudio; N J Siegel; R G Shulman
Journal:  Proc Natl Acad Sci U S A       Date:  1986-08       Impact factor: 11.205

Review 7.  New approaches to the treatment of acute renal failure.

Authors:  K M Gaudio; N J Siegel
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

8.  Beneficial effect of thyroxin in the treatment of ischemic acute renal failure.

Authors:  P M Sutter; G Thulin; M Stromski; T Ardito; K M Gaudio; M Kashgarian; N J Siegel
Journal:  Pediatr Nephrol       Date:  1988-01       Impact factor: 3.714

  8 in total

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