Methamphetamine-induced striatal dopamine neurotoxicity and cyclooxygenase-2 protein expression in BALB/c mice

Neuropharmacology. 2000 Jan 28;39(3):399-406. doi: 10.1016/s0028-3908(99)00175-6.

Abstract

The expression of cyclooxygenase-2 (COX-2) and striatal dopamine (DA) depletion in BALB/cAnNcrj (BALB/c) mice following a neurotoxic dose of methamphetamine (METH) was investigated. METH-treatment (4 mg/kg x 4, 2 h intervals, s.c.) induced a significant hyperthermia and a persistent depletion of striatal DA levels 72 h after the treatment. COX-2, a marker of the cytotoxic effect of inflammation and oxidative stress and thiobarbituric acid (TBA) were significantly induced in the striatum 72 h after the METH-treatment, but not in the hippocampus. These results suggest that COX-2 may participate in METH-induced neurotoxicity in striatum.

MeSH terms

  • Animals
  • Body Temperature / drug effects
  • Body Temperature / physiology
  • Corpus Striatum / drug effects*
  • Corpus Striatum / metabolism
  • Cyclooxygenase 2
  • Dopamine / metabolism*
  • Dopamine Agents / pharmacology*
  • Isoenzymes / drug effects*
  • Isoenzymes / metabolism
  • Methamphetamine / pharmacology*
  • Mice
  • Mice, Inbred BALB C
  • Prostaglandin-Endoperoxide Synthases / drug effects*
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Thiobarbiturates / metabolism*

Substances

  • Dopamine Agents
  • Isoenzymes
  • Thiobarbiturates
  • Methamphetamine
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • thiobarbituric acid
  • Dopamine