Deficiency in cytosolic malic enzyme does not increase acetaminophen-induced hepato-toxicity

Basic Clin Pharmacol Toxicol. 2008 Jul;103(1):36-42. doi: 10.1111/j.1742-7843.2008.00228.x. Epub 2008 Jul 1.

Abstract

Cytosolic malic enzyme (ME-1) is a nicotinamide adenine dinucleotide phosphate (NADP)-dependent enzyme that generates NADPH. The activity of this enzyme, the reversible oxidative decarboxylation of malate to yield pyruvate, links glycolytic pathway to citric acid cycle. The high level of ME-1 expression in liver, and its involvement in NADPH production, suggests reduced ME-1 activity might compromise hepatic production of reduced glutathione (GSH) by the NADPH-dependent enzyme glutathione reductase, and hence affect xenobiotic detoxification. The role of ME-1 in liver detoxification was evaluated in Mod1 deficient mice (mod1(-/-)) by evaluating their sensitivity to acetaminophen-induced liver injury. The results show that mod1(-/-) mice are not more sensitive to acetaminophen hepato-toxicity. Although GSH levels were initially depleted more in the mod1(-/-) liver than in wild-type controls, the GSH levels recovered quickly. In conclusion, our data indicate that ME-1 deficiency does not adversely affect GSH-dependent detoxification.

MeSH terms

  • Acetaminophen / toxicity*
  • Analgesics / toxicity*
  • Animals
  • Chemical and Drug Induced Liver Injury / enzymology*
  • Chemical and Drug Induced Liver Injury / pathology
  • Cytosol / enzymology
  • Genotype
  • Glutathione / metabolism
  • Liver / enzymology*
  • Liver / pathology
  • Malate Dehydrogenase / genetics
  • Malate Dehydrogenase / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • NADP / metabolism

Substances

  • Analgesics
  • Acetaminophen
  • NADP
  • Malate Dehydrogenase
  • Glutathione