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To make adaptive decisions, we build an internal model of the associative relationships in an environment and use it to make predictions and inferences about specific available outcomes. Detailed, identity-specific cue-reward memories are a core feature of such cognitive maps. Here we used fiber photometry, cell-type and pathway-specific optogenetic manipulation, Pavlovian cue-reward conditioning and decision-making tests in male and female rats, to reveal that ventral tegmental area dopamine (VTA) projections to the basolateral amygdala (BLA) drive the encoding of identity-specific cue-reward memories. Dopamine is released in the BLA during cue-reward pairing; VTA→BLA activity is necessary and sufficient to link the identifying features of a reward to a predictive cue but does not assign general incentive properties to the cue or mediate reinforcement. These data reveal a dopaminergic pathway for the learning that supports adaptive decision-making and help explain how VTA neurons achieve their emerging multifaceted role in learning.
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http://dx.doi.org/10.1038/s41593-024-01586-7 | DOI Listing |
Mol Psychiatry
August 2025
Division of Depression and Anxiety Disorders, McLean Hospital, Department of Psychiatry, Harvard Medical School, Belmont, MA, 02478, USA.
Alcohol seeking during abstinence is mediated in part by strong associations between the pharmacological effects of alcohol and the environment within which alcohol is administered. The amygdala, particularly the basolateral amygdala (BLA), is a key neural substrate of environmental cue and reward associations since it is involved in associative learning and memory recall. However, we still lack a clear understanding of how alcohol affects the activity of BLA neurons, which may encode information that drives environmental cue-dependent, alcohol-related behaviors.
View Article and Find Full Text PDFBehav Brain Res
August 2025
Oral Physiology, Department of Oral Functional Science, Division of Oral Medical Science, Faculty of Dental Medicine and Graduate School of Dental Medicine, Hokkaido University, Japan.
The basolateral amygdala (BLA) plays a critical role in aversive learning and decision‑making, yet its specific contribution to the expression of conditioned taste aversion (CTA) remains incompletely understood. Here, we examined how transient chemogenetic inhibition of the BLA influences licking microstructure and approach-avoidance behavior toward a conditioned saccharin solution. Male C57BL/6 mice received bilateral BLA injections of AAV8‑hSyn‑hM4Di‑mCherry (experimental) or AAV8‑hSyn‑mCherry (control).
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
State Key Laboratory of Medical Neurobiology, Institutes of Brain Science, MOE Frontier Center for Brain Science, Department of Neurology of Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Context-triggered retrieval of drug withdrawal memories (CTR-DWM) is a major cause of drug relapse. Most studies of the context-triggered retrieval of morphine withdrawal memories (CTR-MWM) have mainly focused on the functional interactions within the central structures of the brain. It remains unknown how an increase in corticosterone, which is an important response under drug withdrawal state, participates in CTR-MWM.
View Article and Find Full Text PDFCurr Biol
August 2025
Department of Neurosciences, School of Medicine, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, OH 44106, USA. Electronic address:
The CA3 region of the hippocampus is essential for associative memory. CA3 pyramidal neurons receive three canonical excitatory inputs-recurrent collaterals from other CA3 pyramidal neurons, mossy fiber input from the dentate gyrus (DG), and perforant path input from the entorhinal cortex-that terminate at specific dendritic compartments and have distinct functions. Yet, the additional extrahippocampal inputs to CA3 are less clear.
View Article and Find Full Text PDFJ Comp Neurol
August 2025
Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
The shell of the nucleus accumbens (NAcSh) regulates motivation and reward via its dense projection to the ventral pallidum (VP). This ventral striatopallidal system has also been shown to regulate the activity of midbrain dopamine neurons and the release of dopamine in the NAcSh. The present study applied monosynaptic rabies tracing in the rat to quantify the brain-wide sources of synaptic input to neurons in the medial NAcSh that project to the ventromedial VP.
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