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Lüscher, C.

Publications and source records attributed to Lüscher, C..

2 recordsLinked to original sources

VTA dopamine neurons multiplex external with internal representations of goal-directed action

Dopamine (DA) neurons of the ventral tegmental area (VTA) track external cues and rewards to generate a reward prediction error (RPE) signal during Pavlovian conditioning. Here we explored how RPE is implemented for a self-paced, operant task in freely moving mice. The animal could trigger a reward-predicting cue by remaining in a specific location of an operant box for a brief time before moving to a spout for reward collection. In vivo single-unit recordings revealed phasic responses to the cue and reward in correct trials, while with failures the activity paused, reflecting positive and negative error signals of a reward prediction. In addition, a majority of VTA DA neurons also encoded parameters of the goal-directed action (e.g. movement velocity, acceleration, distance to goal and licking) by changes in tonic firing rate. Such multiplexing of individual neurons was only apparent while the mouse was engaged in the task. We conclude that a multiplexed internal representation during the task modulates VTA DA neuron activity, indicating a multimodal prediction error that shapes behavioral adaptation of a self-paced goal-directed action.

neuroscience

Dopamine neurons projecting to medial shell of the nucleus accumbens drive heroin reinforcement

The dopamine (DA) hypothesis posits the increase of mesolimbic dopamine levels as a defining commonality of addictive drugs, initially causing reinforcement, eventually leading to compulsive consumption. While much experimental evidence from psychostimulants supports this hypothesis, it has been challenged for opioid reinforcement. Here, we use genetically encoded DA and calcium indicators as well as cFos to reveal that heroin activates DA neurons located in the medial part of the VTA, preferentially projecting to the medial shell of the nucleus accumbens (NAc). Chemogenetic and optogenetic manipulations of VTA DA or GABA neurons establish a causal link to heroin reinforcement. Inhibition of DA neurons blocked heroin self-administration, while heroin inhibited optogenetic self-stimulation of DA neurons. Likewise, heroin occluded the self-inhibition of VTA GABA neurons. Together, these experiments support a model of disinhibition of a subset of VTA DA neurons in opioid reinforcement.

neuroscience