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Lowes, D. C.

Publications and source records attributed to Lowes, D. C..

3 recordsLinked to original sources

Striatal acetylcholine enables latent-state creation during reversal learning

Like dopamine, acetylcholine is modulated in the striatum by reward-predicting cues and outcomes, yet its computational role remains unclear. Here, we manipulated dorsomedial striatal acetylcholine in mice performing a reversal learning task using genetic and physiologically guided optogenetic approaches. Inhibiting phasic acetylcholine modulation impaired reversal learning, while enhancing modulation during non-rewarded trials facilitated reversal learning. Trial-by-trial acetylcholine dynamics were best explained by a reinforcement learning model in which new latent states are created when experience is poorly explained by existing states. A circuit-constrained model further suggested that acetylcholine promotes plasticity when reward-omission is ambiguous, leading to a surprising prediction: making reward omission explicit should reduce the need for acetylcholine. We confirmed this in a new experiment in which an auditory omission cue substantially reduced the reversal-learning deficit caused by genetic acetylcholine knockdown. These findings suggest that striatal acetylcholine supports reversal learning by promoting state construction in reinforcement learning.

neuroscience↗

Altered striatal dopamine regulation in ADGRL3 knockout mice

Dopaminergic signaling is essential for regulating movement, learning, and reward. Disruptions in this system are linked to neuropsychiatric disorders such as ADHD. ADGRL3, an adhesion G protein-coupled receptor highly expressed in the brain, is genetically associated with increased ADHD risk. ADGRL3 knockout in animals alters expression of dopaminergic markers and induces dopamine-related behavioral changes. However, its precise role in modulating dopamine signaling remains unclear. We investigated how ADGRL3 knockout affects striatal dopamine release in mice using ex vivo fast-scan cyclic voltammetry and in vivo fiber photometry with a dopamine sensor. Ex vivo measurements showed increased electrically-evoked dopamine release across the striatum. Conversely, in vivo recordings revealed reduced task-induced dopamine signals in the nucleus accumbens during an operant fixed interval task. This reduction was not due to impaired dopamine availability, as amphetamine-evoked release was unchanged. These findings suggest ADGRL3 modulates dopamine release in complex ways via different pre- and postsynaptic mechanisms.

neuroscience↗

Ventral tegmental area GABA neurons mediate stress-induced anhedonia.

Stressful experiences frequently precede depressive episodes1. Depression results in anhedonia, or disrupted reward-seeking, in most patients2. In humans3,4 and rodents5,6, stress can disrupt reward-seeking, providing a potential mechanism by which stress can precipitate depression7-9. Yet despite decades investigating how stress modulates dopamine neuron transmission between the ventral tegmental area (VTA) and nucleus accumbens (NAc), the underpinnings of the stress-anhedonia transition remain elusive10-13. Here we show that during restraint stress, VTA GABA neurons drive low frequency NAc LFP oscillations, rhythmically modulating NAc firing rates. The strength of these stress-induced NAc oscillations predict the degree of impaired reward-seeking upon release from restraint. Inhibiting VTA GABA neurons disrupts stress-induced NAc oscillations and reverses the effect of stress on reward-seeking. By contrast, mimicking these oscillations with rhythmic VTA GABA stimulation in the absence of stress blunts subsequent reward-seeking. These experiments demonstrate that VTA GABA inputs to the NAc are both necessary and sufficient for stress-induced decreases in reward seeking behavior, elucidating a key circuit-level mechanism underlying stress-induced anhedonia.

neuroscience↗