Role of 5-HT 2A receptors in the effects of ayahuasca on ethanol self-administration using a two-bottle choice paradigm in male mice

Ayahuasca has been proposed as a potential treatment of alcohol (ethanol) use disorder (AUD). The serotonin 5-HT receptor agonist N,N-dimethyltryptamine (DMT) is the main psychoactive component of ayahuasca, suggesting that its therapeutic effects may be mediated by 5-HT receptors. The aim of the pr...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Psychopharmacology (Berlin, Germany) Germany), 2022-06, Vol.239 (6), p.1679
Hauptverfasser: Serra, Yasmim A, Barros-Santos, Thaísa, Anjos-Santos, Alexia, Kisaki, Natali D, Jovita-Farias, Caio, Leite, João P C, Santana, Maria C E, Coimbra, João P S A, de Jesus, Nailton M S, Sulima, Agnieszka, Barbosa, Paulo C R, Malpezzi-Marinho, Elena L A, Rice, Kenner C, Oliveira-Lima, Alexandre J, Berro, Laís F, Marinho, Eduardo A V
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Ayahuasca has been proposed as a potential treatment of alcohol (ethanol) use disorder (AUD). The serotonin 5-HT receptor agonist N,N-dimethyltryptamine (DMT) is the main psychoactive component of ayahuasca, suggesting that its therapeutic effects may be mediated by 5-HT receptors. The aim of the present study was to investigate the effects of ayahuasca on the expression of ethanol self-administration using a two-bottle choice procedure and the role of 5-HT receptors in those effects. Male mice had intermittent access to ethanol (10% v/v) in a two-bottle choice procedure for 30 days. Animals were then submitted to 3 treatment phases, each followed by ethanol re-exposure tests. During the treatment phase, every 3 days, animals received i.p. injections of either vehicle or the 5-HT receptor antagonist M100907 (M100, 1 mg/kg) followed by an i.g. (gavage) administration of vehicle or ayahuasca (100 mg/kg) and were exposed to the self-administration apparatus with no ethanol availability. During re-exposure tests, animals were submitted to the same conditions as during acquisition, with no treatments prior to those sessions. Treatment with ayahuasca blocked the expression of ethanol self-administration, decreasing ethanol intake and preference during re-exposure tests. Pretreatment with M100 blocked the effects of ayahuasca on ethanol drinking without significantly attenuating ethanol self-administration. Treatment with ayahuasca during alcohol abstinence blocked the expression of alcohol self-administration in mice, and 5-HT receptor activation is critical for those effects to emerge. Our findings support a potential for ayahuasca and other 5-HT receptor agonists as adjunctive pharmacotherapies for the treatment of AUD.
ISSN:1432-2072
DOI:10.1007/s00213-022-06104-w