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Radioligand-binding study of noribogaine, a likely metabolite of ibogaine.

S M Pearl, K Herrick-Davis, Milt Teitler, Stanley D Glick

Brain Research March 27, 1995 DOI: 10.1016/0006-8993(95)00123-8 (opens in new tab)

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AI-extracted from the abstract
Characteristics Radioligand-binding study Peer reviewed
Topics Ibogaine
Citations 78
Key points Noribogaine has higher affinity than ibogaine for kappa, mu, and delta opioid receptors, suggesting it may contribute to ibogaine's pharmacological effects.

Abstract

Radioligand-binding studies were performed to ascertain the actions of noribogaine, a suspected metabolite of ibogaine, on opioid receptors. Consistent with previous results, ibogaine showed highest affinity for kappa opioid receptors (Ki = 3.77 +/- 0.81 microM), less affinity for mu receptors (Ki = 11.04 +/- 0.66 microM) and no affinity for delta receptors (Ki > 100 microM). Noribogaine showed a higher affinity than ibogaine for all of the opioid receptors: kappa Ki = 0.96 +/- 0.08 microM, mu Ki = 2.66 +/- 0.62 microM and delta Ki = 24.72 +/- 2.26 microM. These data suggest that noribogaine is active in vivo and that it may contribute to ibogaine's pharmacological effects.

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