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Chalencon, L.

Publications and source records attributed to Chalencon, L..

2 recordsLinked to original sources

Cell-type-specific encoding of effort-based decision-making in the dorsal raphe nucleus

Effort-based decision-making, the process of weighing reward benefits against effort costs, is essential for adaptive behavior. Although the dorsal raphe nucleus (DRN) contributes to reward processing and effort-related behaviors, how specific DRN neuronal subtypes contribute to effort-based decision-making remains poorly understood. Using fiber photometry to record DRN serotonergic and GABAergic neurons during an effort-based decision-making task, we found that tonic fluctuations in DRN serotonergic activity were selectively associated with persistent selection of the high-value option. Furthermore, we found that while neither neuronal population was sensitive to relative reward magnitude, effort expenditure selectively enhanced decision- and reward-related signals carried by serotonergic and GABAergic neurons, respectively. Together, these findings support a cell type-specific model in which serotonergic activity provides a signal linking persistent motivational states to effortful choice, whereas GABAergic activity may contribute to evaluating or updating reward outcomes after effort expenditure. SIGNIFICANCE STATEMENTChoosing whether a reward is worth the effort required to obtain it is essential for adaptive behavior, yet the neural mechanisms underlying this process remain incompletely understood. Here, we identify distinct contributions of serotonin- and GABAergic neurons in the dorsal raphe nucleus, a major source of brain serotonin, to effort-based decision-making. Serotonergic neurons were preferentially engaged in sustained motivational state and action selection, and GABAergic neurons in the processing of reward outcomes following costly actions. Our findings reveal a cell type-specific organization of effort-based reward seeking in the dorsal raphe nucleus and provide a framework for understanding how motivational states, decisions, and reward outcomes are coordinated.

neuroscience↗

Cellular and molecular coding of habit-driven behavior in the dorsal raphe nucleus

Chronic stress has potent effects on reward-seeking behavior, reducing hedonic drive but also biasing individuals toward habitual responding at the expense of goal-directed action. While prior studies have implicated corticostriatal circuits in these shifts, the contribution of the dorsal raphe nucleus (DRN) - a central neuromodulatory hub that regulates motivational states - remains poorly understood. Here, we identify a key role for DRN neurons in mediating stress-induced transitions from goal-directed to habit-driven behavior. Using two-photon calcium imaging in awake behaving mice, we show that DRN neurons encode representations of both effort expenditures and reward acquisition that are integrated at the single-neuron level. Chronic stress selectively enhances reward-related responses in habit-driven individuals, and deficits in reward-related activity in DRN neurons predict future habit formation after chronic stress. Single-nucleus transcriptional profiling revealed that chronic stress drives habit-related gene expression changes in GABAergic DRN neurons, including upregulation of genes implicated in synapse function and inhibitory signaling, and identified potential pharmacological treatment targets. Optogenetic inhibition of DRN GABA neurons rescued stress effects on habit formation, driving stable shifts in operant responding that persisted for days. Together, these findings establish the DRN as a critical modulator of stress-induced behavioral inflexibility, and identify a new role for DRN GABAergic neurons in determining stress susceptibility and driving stable and persistent switches in operant responding during recovery from chronic stress.

neuroscience↗