Effect of d-amphetamine repeated administration on rat antioxidant defences

Arch Toxicol. 1999 Mar;73(2):83-9. doi: 10.1007/s002040050591.

Abstract

The purpose of this study was to evaluate rat tissue antioxidant status after repeated administration of d-amphetamine. Three groups of four rats each were used: control, d-amphetamine sulphate dosed (s.c., 20 mg/kg per day), and pair-fed. After 14 days of d-amphetamine daily administration, superoxide dismutase (CuZnSOD and MnSOD), catalase, glutathione peroxidase (GPx), glutathione reductase (GRed), glutathione-S-transferase (GST), glutathione (GSH), cysteine and thiobarbituric acid reactive substances (TBARS) were measured in liver, kidney, and heart. Various serum and urine parameters were also analysed. d-Amphetamine treatment induced an increase of liver GSH, as well as a decrease of cysteine and MnSOD levels in this organ. A small increase in serum transaminases was also observed in comparison to the pair-fed group. Hepatic levels of TBARS, GPx, GRed and CuZnSOD were found to be similar among the three groups of rats. d-Amphetamine treatment induced an increase of kidney GST, GRed and catalase levels, and an elevation of N-acetyl-beta-D-glucosaminidase efflux to the urine, accompanied by a decrease in urinary creatinine, compared to the pair-fed group. In d-amphetamine treated animals, heart cysteine levels were significantly depleted when compared to the pair-fed group, but all three groups of rats were found to have similar heart antioxidant enzyme levels. These results indicate that repeated administration of d-amphetamine caused a certain degree of stress in liver and kidney, which was followed by adaptations of antioxidant defences. The mechanisms involved in d-amphetamine-induced toxicity may explain the different adaptations observed for the studied organs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Weight / drug effects
  • Cysteine / analysis*
  • Dextroamphetamine / administration & dosage
  • Dextroamphetamine / metabolism
  • Dextroamphetamine / toxicity*
  • Drinking / drug effects
  • Eating / drug effects
  • Liver / drug effects
  • Liver / enzymology*
  • Male
  • Organ Specificity
  • Oxidation-Reduction / drug effects*
  • Oxidative Stress
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Reactive Oxygen Species / metabolism*
  • Time Factors
  • Urine / chemistry

Substances

  • Reactive Oxygen Species
  • Cysteine
  • Dextroamphetamine