Artigo Acesso aberto Produção Nacional Revisado por pares

Adenosine A2A Receptors in the Rat Prelimbic Medial Prefrontal Cortex Control Delay-Based Cost-Benefit Decision Making

2018; Frontiers Media; Volume: 11; Linguagem: Inglês

10.3389/fnmol.2018.00475

ISSN

1662-5099

Autores

Douglas Teixeira Leffa, Pablo Pandolfo, Nélio Gonçalves, Nuno J. Machado, Carolina Melo de Souza, Joana I. Real, António C. Silva, Henrique B. Silva, Attila Köfalvi, Rodrigo A. Cunha, Samira G. Ferreira,

Tópico(s)

Receptor Mechanisms and Signaling

Resumo

Adenosine A2A receptors (A2AR) were recently described to control synaptic plasticity and network activity in the prefrontal cortex (PFC). We now probed the role of these PFC A2AR by evaluating the behavioral performance (locomotor activity, anxiety-related behavior, cost-benefit decision making and working memory) of rats upon viral shA2AR-mediated downregulation of A2AR selectively in the prelimbic medial prefrontal cortex (PLmPFC). The most evident alteration observed in shA2AR-treated rats, when compared to sh-control-treated rats, was a decrease in the choice of the large reward upon an imposed delay of 15 seconds assessed in a T-maze-based cost-benefit decision-making paradigm, suggestive of impulsive decision making. Spontaneous locomotion in the open field was not altered, suggesting no changes in exploratory behavior. Furthermore, rats treated with shA2AR in the PLmPFC also displayed a tendency for higher anxiety levels in the elevated plus maze (less entries in the open arms), but not in the open field test (time spent in the center was not affected). Finally, working memory performance was not significantly altered, as revealed by the spontaneous alternation in the Y-maze test and the latency to reach the platform in the repeated trial Morris water maze. These findings constitute the first direct demonstration of a role of PFC A2AR in the control of behavior in physiological conditions, showing their major contribution for the control of delay-based cost-benefit decisions.

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