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Millan, Z.

Publications and source records attributed to Millan, Z..

2 recordsLinked to original sources

Representational geometry of punishment learning across basolateral amygdala neurons

Punishment learning allows animals to suppress actions that cause harm while maintaining actions that earn reward. Although the basolateral amygdala is necessary for punishment learning, how its population activity changes across learning, and how this activity reflects an action's consequences, remain unknown. We used longitudinal calcium imaging to track 1,147 basolateral amygdala neurons in male mice across instrumental training, punishment, choice test, and punishment extinction. Punishment learning transformed basolateral amygdala neuron activity associated with the punished action. This activity diverged from that associated with the unpunished action and became aligned with activity evoked by the punisher itself. This alignment was action and contingency specific. It preserved the direction of individual neurons' responses to the punisher: neurons activated by the punisher become more activated by the punished action alone, whereas neurons inhibited by the punisher become more inhibited by the punished action alone. We then asked whether reward and punishment were encoded separately or on a common value dimension across basolateral amygdala neurons. Punishment added a strong shock component to action-related activity without reducing its reward component, while reward and shock themselves occupied largely orthogonal population directions. Thus, during punishment learning, basolateral amygdala population activity can encode opposing consequences of the same action instead of simply changing what that action is worth.

neuroscience↗

Dual GLP-1/FGF21 agonism suppresses voluntary alcohol consumption, alcohol choice, and nucleus accumbens dopamine modulation

Excessive alcohol consumption remains a major public health challenge with limited therapeutic options. Both glucagon-like peptide-1 (GLP-1) and fibroblast growth factor-21 (FGF21) independently regulate alcohol intake through complementary metabolic and reward pathways, but their combined potential has not been explored. Here, we report that a long-acting dual agonist, GLP1-ELP-FGF21 modulates behavioural, neurophysiological, and cognitive components of alcohol seeking in mice. A single GLP1-ELP-FGF21 dose reversibly reduces voluntary alcohol intake for at least 72 hours in male mice, has sustained effects in female mice, and markedly blunts nucleus accumbens dopamine transients aligned to the initiation and termination of lick bouts during alcohol consumption. To assess its effects on decision-making, we used a novel two-choice (alcohol versus food) decision task modelled with evidence-accumulation frameworks. Alcohol choice behaviour conformed to evidence accumulation decision models: Linear Ballistic Accumulator (LBM) and Racing diffusion models (RDM). Critically, GLP1-ELP-FGF21 selectively reduces choices for alcohol and slows the latent accumulation rate for alcohol options, without affecting food-directed choice or non-decision processes. Sensory-specific satiety devaluation confirms that reductions in reward value are explained by reductions in accumulation rates. Together, these results highlight GLP1-ELP-FGF21 as a therapeutic strategy for alcohol use disorder via modulation of central reward pathways and decision-making when confronted with alcohol reward

animal behavior and cognition↗