Cocaine-induced increases in motivation require 2-arachidonoylglycerol mobilization and CB1 receptor activation in the ventral tegmental area

Autor(es)

Engi, Sheila A. ^{[1, 2]} ; Beebe, Erin J. ^[2] ; Ayvazian, Victoria M. ^[2] ; Cruz, Fabio C. ^[1] ; Cheer, Joseph F. ^{[3, 2]} ; Wenzel, Jennifer M. ^[2] ; Zlebnik, Natalie E. ^[2]

Afiliação do(s) autor(es)

^[1] Univ Fed Sao Paulo UNIFESP, Dept Pharmacol, Sao Paulo, SP - Brazil

^[2] Univ Maryland, Sch Med, Dept Anat & Neurobiol, Baltimore, MD 21201 - USA

^[3] Univ Maryland, Sch Med, Dept Psychiat, Baltimore, MD 21201 - USA

• Tipo de documento: Artigo Científico
• Fonte: Neuropharmacology; v. 193, AUG 1 2021.
• Citações Web of Science: 0

Resumo

A wide body of evidence supports an integral role for mesolimbic dopamine (DA) in motivated behavior. In brief, drugs that increase DA in mesolimbic terminal regions, like cocaine, enhance motivation, while drugs that decrease DA concentration reduce motivation. Data from our laboratory and others shows that phasic activation of mesolimbic DA requires signaling at cannabinoid type-1 (CB1) receptors in the ventral tegmental area (VTA), and systemic delivery of CB1 receptor antagonists reduces DA cell activity and attenuates motivated behaviors. Recent findings demonstrate that cocaine mobilizes the endocannabinoid 2-arachidonoylglycerol (2-AG) in the VTA to cause phasic activation of DA neurons and terminal DA release. It remains unclear, however, if cocaineinduced midbrain 2-AG signaling contributes to the motivation-enhancing effects of cocaine. To examine this, we trained male and female rats on a progressive ratio (PR) task for a food reinforcer. Each rat underwent a series of tests in which they were pretreated with cocaine alone or in combination with systemic or intra-VTA administration of the CB1 receptor antagonist rimonabant or the 2-AG synthesis inhibitor tetrahydrolipstatin (THL). Cocaine increased motivation, measured by augmented PR breakpoints, while rimonabant dose-dependently decreased motivation. Importantly, intra-VTA administration of rimonabant or THL, at doses that did not decrease breakpoints on their own, blocked systemic cocaine administration from increasing breakpoints in male and female rats. These data suggest that cocaine-induced increases in motivation require 2-AG signaling at CB1 receptors in the VTA and may provide critical insight into cannabinoid-based pharmacotherapeutic targets for the successful treatment of substance abuse. (AU)

• Processo FAPESP: 19/23286-3 - Efeitos da exposição a canabinóides no desenvolvimento da circuitaria dopaminérgica mesocorticolímbica de adolescentes
• Beneficiário: Sheila Antonagi Engi
• Modalidade de apoio: Bolsas no Exterior - Estágio de Pesquisa - Pós-Doutorado