Effects of acute hyperammonemia in vivo on oxidative metabolism in nonsynaptic rat brain mitochondria

Metab Brain Dis. 1997 Mar;12(1):69-82. doi: 10.1007/BF02676355.

Abstract

The effects of hyperammonemia induced in vivo by injecting rats with ammonium acetate on oxidative phosphorylation, malate-aspartate shuttle, some related enzyme activities and metabolite levels in brain mitochondria were studied ex vivo. Rats were found to be either ammonia-sensitive (showing convulsions) or ammonia-resistant (without convulsions) after intraperitoneal injection of ammonium acetate (7 mmol/kg). Ammonium acetate administration to ammonia-sensitive rats led to inhibition of State 3 rates of brain mitochondria utilizing pyruvate, glutamate, isocitrate, and succinate as substrates and to decreased respiratory control index. In brain mitochondria isolated from ammonia-resistant animals, the ammonia-induced effect on such State 3 rates was not observed. In brain mitochondria from hyperammonemic rats without convulsions, a small increase in the activity of malate dehydrogenase was observed; glutamate dehydrogenase, succinate dehydrogenase, and aspartate aminotransferase were not affected. In brain mitochondria from rats with ammonia-induced convulsions, the activities of malate dehydrogenase and succinate dehydrogenase were reduced significantly. Ammonium acetate injection to rats was associated with a 5-fold increase in the brain mitochondrial ammonium ion content and a decrease (ca. 50%) in brain mitochondrial glutamate and aspartate; brain mitochondrial malate and 2-oxoglutarate levels remained unchanged. The rate of the malate-aspartate shuttle in brain mitochondria of hyperammonemic rats was decreased by 20% as compared to corresponding rate in control rats. We conclude that acute administration of ammonium acetate induces serious disturbances in the electron-transport chain, interferences of the malate-aspartate shuttle, alterations of the levels of shuttle intermediates and inhibition of the activities of malate and succinate dehydrogenases in brain mitochondria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / pharmacology
  • Ammonia / blood*
  • Animals
  • Aspartate Aminotransferases / metabolism
  • Aspartic Acid / metabolism
  • Brain Chemistry / drug effects
  • Brain Chemistry / physiology*
  • Glutamate Dehydrogenase / metabolism
  • In Vitro Techniques
  • Kinetics
  • Malate Dehydrogenase / metabolism
  • Malates / metabolism
  • Male
  • Mitochondria / drug effects
  • Mitochondria / enzymology
  • Mitochondria / metabolism*
  • Oxidation-Reduction
  • Oxygen Consumption / drug effects
  • Oxygen Consumption / physiology
  • Rats
  • Rats, Wistar
  • Succinate Dehydrogenase / metabolism

Substances

  • Acetates
  • Malates
  • Aspartic Acid
  • Ammonia
  • Malate Dehydrogenase
  • Succinate Dehydrogenase
  • Glutamate Dehydrogenase
  • Aspartate Aminotransferases
  • ammonium acetate