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Ibogaine selectively inhibits nicotinic receptor-mediated catecholamine release.

A S Schneider, J E Nagel, S J Mah

European Journal of Pharmacology December 19, 1996 DOI: 10.1016/s0014-2999(96)00815-1 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics In vitro experimental study Peer reviewed
Population Cultured chromaffin cells
Intervention Ibogaine
Dose 1-10 µM, 100 µM
Topics Ibogaine
Citations 20
Key findings Low concentrations of ibogaine selectively inhibit nicotinic receptor-mediated catecholamine release, indicating action at the nicotinic acetylcholine receptor ion channel.

Abstract

The effects of ibogaine, a putative anti-addictive drug, on stimulated catecholamine release were examined in cultured chromaffin cells to clarify its mechanism(s) of action. Low concentrations of ibogaine (1-10 microM) had a selective inhibitory action on nicotinic receptor-mediated catecholamine release, while higher concentrations (100 microM) inhibited additional modes of stimulated catecholamine release. These results suggest a selective inhibitory action of ibogaine at the nicotinic acetylcholine receptor, possibly at the receptor ion channel site.

Comparable studies

Other preclinical and animal studies on ibogaine, most cited first.

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