Ibogaine block of the NMDA receptor: In vitro and in vivo studies

Kang Chen, Tushar G. Kokate, Sean D. Donevan, F. Ivy Carroll, Michael A Rogawski

Research output: Contribution to journalArticle

34 Scopus citations

Abstract

Ibogaine is an hallucinogenic indole alkaloid claimed to have anti- addictive properties. Although its mechanism of action is unknown, binding studies have indicated that the drug may interact with N-methyl-D-aspartate (NMDA) receptors. We further investigated the nature of the interaction between ibogaine and NMDA receptors in voltage clamp and binding studies, and sought to confirm that the drug has NMDA receptor blocking activity in vivo. In whole-cell recordings from cultured rat hippocampal neurons, ibogaine caused a slow, concentration-dependent block of NMDA-induced currents (IC50, 3.1 μM at -60 mV). In contrast, ibogaine failed to affect either kainate- or γ-aminobutyric acid-evoked currents. The blockade of NMDA currents was use- and voltage-dependent, and the long lasting ibogaine block could be occluded by coapplication of Mg2+. Ibogaine also inhibited equilibrium [3H]dizocilpine binding to NMDA receptors in rat forebrain membranes (IC50, 3.2 μM). We conclude that ibogaine is an open channel NMDA receptor antagonist. Administration of ibogaine to mice resulted in complete protection in the maximal electroshock test (ED50, 31 mg/kg, i.p.) and partial protection against NMDA-induced lethality, confirming that ibogaine can block NMDA receptors in vivo.

Original languageEnglish (US)
Pages (from-to)423-431
Number of pages9
JournalNeuropharmacology
Volume35
Issue number4
DOIs
StatePublished - Apr 1996
Externally publishedYes

Keywords

  • [H]dizocilpine binding
  • hippocampus
  • Ibogaine
  • maximal electroshock (MES) test
  • NMDA receptor
  • seizure
  • voltage clamp recording

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Drug Discovery
  • Pharmacology

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