Top-down corticostriatal control of adaptive restraint during motivational conflict

Adaptive behavior under threat requires withholding reward pursuit when past experiences predict danger. Here, we identified a corticostriatal circuit that enables behavioral restraint during motivational conflict. Using a seminaturalistic foraging task in male rats, we found that inactivation of the prelimbic cortex (PL) abolished restraint without impairing memory, and single-unit recordings revealed transient PL firing increases at decision points in conflict trials. c-Fos mapping showed selective engagement of the PL and nucleus accumbens core (NAcC) but not the nucleus accumbens shell. Inactivation further revealed that the anterior NAcC (aNAcC), but not the posterior NAcC, is necessary for restraint as posterior disruption broadly reduced reward-seeking regardless of threat. Silencing PL→aNAcC projections reproduced aNAcC effects without affecting memory or motivation, and this pathway was required under learned, but not innate, threats. Together, these findings identify a corticostriatal pathway through which PL control of aNAcC supports learned threat-guided restraint during reward seeking, revealing a top-down circuit architecture for adaptive action control during motivational conflict.

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Publication Details

Journal
Science Advances
Published
2026-09-11
DOI
https://doi.org/10.1126/sciadv.aeg2327
Primary Topic
Memory and Neural Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Top-down corticostriatal control of adaptive restraint during motivational conflict

Elizabeth Illescas-Huerta, Eduardo Hernández-Ortiz, Francisco Sotres-Bayón
Science Advances
Memory and Neural Mechanisms
article

Top-down corticostriatal control of adaptive restraint during motivational conflict

Elizabeth Illescas-Huerta, Eduardo Hernández-Ortiz, Francisco Sotres-Bayón
article en

Abstract

Adaptive behavior under threat requires withholding reward pursuit when past experiences predict danger. Here, we identified a corticostriatal circuit that enables behavioral restraint during motivational conflict. Using a seminaturalistic foraging task in male rats, we found that inactivation of the prelimbic cortex (PL) abolished restraint without impairing memory, and single-unit recordings revealed transient PL firing increases at decision points in conflict trials. c-Fos mapping showed selective engagement of the PL and nucleus accumbens core (NAcC) but not the nucleus accumbens shell. Inactivation further revealed that the anterior NAcC (aNAcC), but not the posterior NAcC, is necessary for restraint as posterior disruption broadly reduced reward-seeking regardless of threat. Silencing PL→aNAcC projections reproduced aNAcC effects without affecting memory or motivation, and this pathway was required under learned, but not innate, threats. Together, these findings identify a corticostriatal pathway through which PL control of aNAcC supports learned threat-guided restraint during reward seeking, revealing a top-down circuit architecture for adaptive action control during motivational conflict.

Science AdvancesVol. 12(37)
Universidad Nacional Autónoma de México (MX)
International Brain Research Organization, Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México
Peace, Justice and strong institutions
Openalex Percentile: Top 10%
Memory and Neural Mechanisms
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