Back to Search Start Over

Harmine impairs memory performance of treated rats and nontreated cagemates

Authors :
José Alexandre de Souza Crippa
Antonio Waldo Zuardi
Jaime Eduardo Cecílio Hallak
Fernanda Fiel Peres
Suzy S. Niigaki
Tânia Cristina Libânio
Raí A. Eufrasio
Regina H. Silva
Mariana Bendlin Calzavara
Vanessa C. Abílio
Source :
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual), Universidade de São Paulo (USP), instacron:USP
Publication Year :
2021

Abstract

The interest in psychedelic substances as potential treatments for psychiatric disorders is increasing. The β-carboline harmine, an Ayahuasca component, presents hallucinogenic and antidepressant effects. Although Ayuahuasca-and consequently harmine-is usually consumed in rituals, the role of social contexts in the behavioral effects of harmine has not been investigated yet. In this sense, affective states may modulate cohabitants' behavior, including learning/memory. This work investigates the effects of harmine on the learning/memory performance of rats evaluated on the contextual and tone fear conditioning (CFC and TFC) and on the plus-maze discriminative avoidance (PMDAT) tasks. The possible influence of a harmine-treated cohabitant was assessed by evaluating rats housed in homogeneous cages-where all the animals were acutely administered with the same treatment (vehicle, 5, 10, or 15 mg/kg harmine), and in heterogeneous cages-where each animal received a different drug treatment. The main results are: (a) harmine impaired CFC (10 mg/kg) and PMDAT discrimination (all doses); and (b) harmine caused a memory deficit in CFC, TFC, and PMDAT of untreated rats kept in heterogeneous cages. Our results show that harmine induces a memory deficit in tasks with emotional contexts. Further, the cohabitation with animals treated with this drug also seems to impair memory performance of untreated animals. (PsycInfo Database Record (c) 2021 APA, all rights reserved).

Details

ISSN :
19362293
Volume :
30
Issue :
6
Database :
OpenAIRE
Journal :
Experimental and clinical psychopharmacology
Accession number :
edsair.doi.dedup.....2c302d29877e380adb5bb375945ddc3f