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Learning and memory (L&M) are critically modulated by dopaminergic (DA) projections from the ventral tegmental area (VTA) to distributed forebrain circuits. Disruption of these pathways is implicated in cognitive and emotional dysfunction across neuropsychiatric disorders, yet how these projections generate diverse and sometimes opposing behavioral outcomes remains unresolved. Here, we synthesize recent optogenetic and chemogenetic studies to examine the roles of VTA DA projections to the prefrontal cortex (PFC), hippocampus (HPF), and basolateral amygdala (BLA) across distinct L&M phases. We synthesize evidence showing that comparable patterns of dopaminergic activity can produce bidirectional behavioral effects depending on both the target circuit and the learning phase, particularly in paradigms such as fear learning and extinction. We propose a unifying "phase-by-target" framework in which VTA DA acts as a phase-specific instructional signal whose functional outcome is determined by the engaged circuit. Within this model, DA facilitates contextual encoding in the HPF, supports inhibitory control in the PFC, and enables associative updating in the BLA. This framework reconciles conflicting findings across the literature and suggests that pathological states may arise from mismatches between dopaminergic signaling, learning phase, and circuit engagement. By providing a circuit-level account of DA function, this model identifies circuit-specific vulnerabilities as potential therapeutic targets in neuropsychiatric and neurodegenerative disorders.
Kiren et al. (Tue,) studied this question.
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