Adaptation of hepatic ammonia metabolism after chronic valproate administration in epileptics treated with phenytoin

Eur Neurol. 1985;24(3):191-5. doi: 10.1159/000115793.

Abstract

The effects of phenytoin (PHT) on the modifications of ammonia (NH+4) metabolism caused by sodium valproate (VPA) are here studied in order to identify the drug combinations susceptible of evoking stuporous states in epileptics, a rare condition attributed to a hyperammonemic encephalopathy induced by VPA. During chronic treatment with PHT or VPA-PHT, the acute injection of VPA increases the kidney's output of NH+4. During chronic PHT treatments, the acute injection of VPA modifies the liver's NH+4 metabolism and the arterial hyperammonemia is high (mean = 90 mumol/l). During chronic VPA-PHT treatments, the acute injection of VPA does not affect the hepatic NH+4 metabolism, suggesting that adaptation occurs, and the arterial hyperammonemia is moderate (mean = 60 numol/l). Disturbances of the hepatic adaptive mechanisms may explain certain complications observed during multiple-drug regimens.

MeSH terms

  • Adaptation, Physiological
  • Adult
  • Ammonia / blood
  • Ammonia / metabolism*
  • Drug Interactions
  • Drug Therapy, Combination
  • Epilepsy / blood
  • Epilepsy / drug therapy*
  • Epilepsy / metabolism
  • Humans
  • Kidney / metabolism
  • Liver / metabolism*
  • Middle Aged
  • Phenytoin / pharmacology*
  • Phenytoin / therapeutic use
  • Valproic Acid / adverse effects
  • Valproic Acid / pharmacology*
  • Valproic Acid / therapeutic use

Substances

  • Valproic Acid
  • Phenytoin
  • Ammonia