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Noribogaine acute administration in rats promotes wakefulness and suppresses REM sleep.

Juan Pedro Castro-Nin, Diego Serantes, Paola Rodríguez, Bruno González, Ignacio Carrera, Pablo Torterolo, Joaquín González

Psychopharmacology July 1, 2024 DOI: 10.1007/s00213-024-06572-2 via PubMed

Summary

AI-generated from the abstract

Noribogaine, the main metabolite of the psychedelic ibogaine, promotes wakefulness while reducing slow-wave sleep and blocking REM sleep in rats, according to polysomnographic recordings. This pattern of sleep/wake alterations is similar to that previously reported for ibogaine itself. The findings provide new evidence on how iboga alkaloids act in the brain, suggesting that noribogaine contributes to the sleep-suppressing effects observed after ibogaine administration.

Study at a glance

Characteristics Experimental study Peer reviewed
Population Rats
Intervention Noribogaine
Topics Ibogaine
Keywords Psychedelics Key metabolite Compounds Sleep physiology sleep
Citations 4
Key finding Noribogaine promotes wakefulness, reduces slow-wave sleep, and blocks REM sleep in rats, mirroring the effects of ibogaine.

Abstract

Ibogaine is a potent atypical psychedelic that has gained considerable attention due to its antiaddictive and antidepressant properties in preclinical and clinical studies. Previous research from our group showed that ibogaine suppresses sleep and produces an altered wakefulness state, which resembles natural REM sleep. However, after systemic administration, ibogaine is rapidly metabolized to noribogaine, which also shows antiaddictive effects but with a distinct pharmacological profile, making this drug a promising therapeutic candidate. Therefore, we still ignore whether the sleep/wake alterations depend on ibogaine or its principal metabolite noribogaine. To answer this question, we conducted polysomnographic recordings in rats following the administration of pure noribogaine. Our results show that noribogaine promotes wakefulness while reducing slow-wave sleep and blocking REM sleep, similar to our previous results reported for ibogaine administration. Thus, we shed new evidence on the mechanisms by which iboga alkaloids work in the brain.

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