Mindscape Collective is now The Consciousness Library. Same library, new name. You may need to sign in again. About the change
Skip to content

Christina M. Ruiz

2 papers in the library · 1 citation · publishing 2024-2025

Papers

Adolescent THC impacts on mPFC dopamine-mediated cognitive processes in male and female rats

bioRxiv (Cold Spring Harbor Laboratory) April 15, 2024 Maricela X. Martinez, Vanessa Alizo Vera, Christina M. Ruiz et al. 1 citation preprint

Adolescent exposure to THC, the main psychoactive component of cannabis, persistently alters dopamine-dependent cognitive functions in a sex-specific manner in rats. Adult rats treated with THC during adolescence showed reduced acquisition of cue-guided reward seeking, but minimal changes in set-shifting or decision-making under uncertainty. When given amphetamine, these rats were more sensitive to its effects on reducing preference for improbable rewards compared to controls. Directly stimulating dopamine neurons in the ventral tegmental area or their projections to the medial prefrontal cortex did not affect decision-making in control rats, but slightly disrupted choices in THC-exposed rats. These results indicate that adolescent THC exposure has specific, lasting effects on cognition and amphetamine sensitivity that may not involve direct dopamine pathway changes.

Adolescent THC impacts on mPFC dopamine-mediated cognitive processes in male and female rats.

Psychopharmacology February 1, 2025 Maricela X. Martinez, Vanessa Alizo Vera, Christina M. Ruiz et al.

Adolescent THC exposure in rats leads to sex-dependent effects on learning to seek rewards guided by cues, but has minimal impact on cognitive flexibility or decision-making under uncertainty. Adult rats treated with THC during adolescence showed reduced discounting of improbable reward options when given amphetamine, indicating heightened sensitivity to dopamine augmentation. Direct chemogenetic stimulation of dopamine neurons in the ventral tegmental area or their projections to the medial prefrontal cortex did not alter decision-making in control rats, but slightly disrupted choices in THC-exposed rats. These findings suggest that adolescent THC exposure produces specific, persistent cognitive changes that may alter responses to amphetamine through mechanisms independent of the VTA-mPFC dopamine pathway.