Protective effects of isoliquiritigenin against methamphetamine-induced neurotoxicity in mice

J Pharmacol Sci. 2009 Oct;111(2):216-20. doi: 10.1254/jphs.09153sc.

Abstract

Isoliquiritigenin (ISL) suppresses cocaine-induced extracellular dopamine levels and has a neuroprotective effect in cocaine-treated rat brain. Here, we examine the effect of ISL on methamphetamine-induced striatal neurotoxicity. Repeated injections of methamphetamine cause the loss of striatal dopamine transporter (DAT) and tyrosine hydroxylase (TH). Intraperitoneal injection of ISL prior to methamphetamine injection significantly prevented methamphetamine-induced reduction of DAT and TH. ISL also suppressed methamphetamine-induced activation of glial cells. Moreover, ISL impeded the expression of nitric oxide synthase and the activation of NF-kappaB through blockage of its phosphorylation. Our results suggest that ISL protects against methamphetamine-induced neurotoxicity by inhibition of NF-kappaB activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chalcones / pharmacology*
  • Corpus Striatum / drug effects
  • Cytoprotection*
  • Dopamine Plasma Membrane Transport Proteins / metabolism
  • Immunohistochemistry
  • Male
  • Methamphetamine / antagonists & inhibitors*
  • Methamphetamine / toxicity
  • Mice
  • Mice, Inbred C57BL
  • Neuroglia / drug effects
  • Neurotoxicity Syndromes / metabolism*
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Chalcones
  • Dopamine Plasma Membrane Transport Proteins
  • Methamphetamine
  • isoliquiritigenin
  • Tyrosine 3-Monooxygenase