Your browser doesn't support javascript.
loading
Role of 5-HT2A receptors in the effects of ayahuasca on ethanol self-administration using a two-bottle choice paradigm in male mice.
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.
Afiliación
  • Serra YA; Department of Health Sciences, Universidade Estadual de Santa Cruz, Rod. Ilhéus/Itabuna, Km 16, Ilhéus, BA, 45662-0, Brazil.
  • Barros-Santos T; Department of Biological Sciences, Universidade Estadual de Santa Cruz, Ilhéus, BA, Brazil.
  • Anjos-Santos A; Drug Design and Synthesis Section, Molecular Targets and Medications Discovery Branch, National Institute On Drug Abuse and the National Institute On Alcohol Abuse and Alcoholism, Bethesda, MD, USA.
  • Kisaki ND; Department of Health Sciences, Universidade Estadual de Santa Cruz, Rod. Ilhéus/Itabuna, Km 16, Ilhéus, BA, 45662-0, Brazil.
  • Jovita-Farias C; Department of Health Sciences, Universidade Estadual de Santa Cruz, Rod. Ilhéus/Itabuna, Km 16, Ilhéus, BA, 45662-0, Brazil.
  • Leite JPC; Department of Biological Sciences, Universidade Estadual de Santa Cruz, Ilhéus, BA, Brazil.
  • Santana MCE; Department of Biological Sciences, Universidade Estadual de Santa Cruz, Ilhéus, BA, Brazil.
  • Coimbra JPSA; Department of Biological Sciences, Universidade Estadual de Santa Cruz, Ilhéus, BA, Brazil.
  • de Jesus NMS; Department of Biological Sciences, Universidade Estadual de Santa Cruz, Ilhéus, BA, Brazil.
  • Sulima A; Drug Design and Synthesis Section, Molecular Targets and Medications Discovery Branch, National Institute On Drug Abuse and the National Institute On Alcohol Abuse and Alcoholism, Bethesda, MD, USA.
  • Barbosa PCR; Department of Health Sciences, Universidade Estadual de Santa Cruz, Rod. Ilhéus/Itabuna, Km 16, Ilhéus, BA, 45662-0, Brazil.
  • Malpezzi-Marinho ELA; Department of Biological Sciences, Universidade Estadual de Santa Cruz, Ilhéus, BA, Brazil.
  • Rice KC; Drug Design and Synthesis Section, Molecular Targets and Medications Discovery Branch, National Institute On Drug Abuse and the National Institute On Alcohol Abuse and Alcoholism, Bethesda, MD, USA.
  • Oliveira-Lima AJ; Department of Health Sciences, Universidade Estadual de Santa Cruz, Rod. Ilhéus/Itabuna, Km 16, Ilhéus, BA, 45662-0, Brazil.
  • Berro LF; Department of Health Sciences, Universidade Estadual de Santa Cruz, Rod. Ilhéus/Itabuna, Km 16, Ilhéus, BA, 45662-0, Brazil. lberro@umc.edu.
  • Marinho EAV; Department of Psychiatry and Human Behavior, Center for Innovation and Discovery in Addictions, University of Mississippi Medical Center, 2500 N State St, Jackson, MS, 39216, USA. lberro@umc.edu.
Psychopharmacology (Berl) ; 239(6): 1679-1687, 2022 Jun.
Article en En | MEDLINE | ID: mdl-35253069
ABSTRACT
RATIONALE Ayahuasca has been proposed as a potential treatment of alcohol (ethanol) use disorder (AUD). The serotonin 5-HT2A receptor agonist N,N-dimethyltryptamine (DMT) is the main psychoactive component of ayahuasca, suggesting that its therapeutic effects may be mediated by 5-HT2A receptors.

OBJECTIVES:

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-HT2A receptors in those effects.

METHODS:

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-HT2A 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.

RESULTS:

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.

CONCLUSIONS:

Treatment with ayahuasca during alcohol abstinence blocked the expression of alcohol self-administration in mice, and 5-HT2A receptor activation is critical for those effects to emerge. Our findings support a potential for ayahuasca and other 5-HT2A receptor agonists as adjunctive pharmacotherapies for the treatment of AUD.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Banisteriopsis Límite: Animals Idioma: En Revista: Psychopharmacology (Berl) Año: 2022 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Banisteriopsis Límite: Animals Idioma: En Revista: Psychopharmacology (Berl) Año: 2022 Tipo del documento: Article País de afiliación: Brasil