Biology subjects

Prevost-Solie, C.

Publications and source records attributed to Prevost-Solie, C..

4 recordsLinked to original sources

bioRxiv2020

Dopamine neurons of the VTA encode active conspecific interaction and promote social learning through social reward prediction error.

Social interactions motivate behavior in many species, facilitating learning, foraging and cooperative behavior. However, how the brain encodes the reinforcing properties of social interactions remains elusive. Here using in vivo recording in freely moving mice, we show that Dopamine (DA) neurons of the Ventral Tegmental Area (VTA) increase their activity during active interactions with unfamiliar conspecific. Using a social instrumental task, we then show that VTA DA neuron activity signals social reward prediction error and drives social reinforcement learning. Thereby, our findings propose that VTA DA neurons are a neural substrate for a social learning signal driving motivated behavior. One Sentence SummaryDA neurons are a substrate for social reward learning through the Social Reward Prediction Error.

neuroscience↗

bioRxiv2019

Superior Colliculus to VTA pathway controls orienting behavior during conspecific interaction.

Social behaviours characterize cooperative, mutualistic aggressive or parental interactions that occurs among conspecifics. Although several neuronal substrates of social behaviour have been identified, whether defined circuits are dedicated to specific aspect of conspecific interaction is still an open question. Ventral Tegmental Area (VTA) contributes to the rewarding properties of conspecific interaction. However, how information related to conspecifics are conveyed to the VTA is still largely unknown. In this study, we identified a population of Superior Colliculus (SC) neurons projecting to the VTA which increase their activity before conspecific interaction and control orienting response towards unfamiliar conspecifics. Finally, we show that SC inputs target a subpopulation of Dopamine (DA) neurons within the VTA that in turn project to dorsolateral striatum (DLS). Our work supports the hypothesis that specialized sub-circuits are dedicated to process different aspect of social interaction.

neuroscience↗

bioRxiv2018

Neuronal signature of social novelty exploration in the VTA: implication for Autism Spectrum Disorder

Novel stimuli attract our attention, promote exploratory behavior, and facilitate learning. Atypical habituation and aberrant novelty exploration have been related with the severity of Autism Spectrum Disorders (ASD) but the underlying neuronal circuits are unknown. Here, we report that dopamine (DA) neurons of the ventral tegmental area (VTA) promote the behavioral responses to novel social stimuli, support preference for social novelty, and mediate the reinforcing properties of novel social interaction. Social novelty exploration is associated with the insertion of calcium-permeable GluA2-lacking AMPA-type glutamate receptors at excitatory synapses on VTA DA neurons. These novelty-dependent synaptic adaptations only persist upon repeated exposure to social stimuli and sustain social interaction. Global or DA neuron-specific inactivation of the ASD risk gene Neuroligin3 alters both social novelty exploration and the reinforcing properties of social stimuli. These behavioral deficits are accompanied by an aberrant expression of non-canonical GluA2-lacking AMPA-receptors at excitatory synapses on VTA DA neurons and an occlusion of novelty-induced synaptic plasticity. Altogether, these findings causally link impaired novelty exploration in an ASD mouse model to VTA DA circuit dysfunction.

neuroscience↗

bioRxiv2018

Acetylcholine-dependent phasic dopamine activity signals exploratory locomotion and choices

Dopamine neurons from the Ventral Tegmental Area (VTA) switch from tonic to phasic burst firing in response to reward-predictive cues and actions. Bursting is influenced by nicotinic acetylcholine receptors (nAChRs), which are not implicated in reinforcement learning, but rather in exploration and uncertainty-seeking. The leading model assigns these functions to tonic dopamine firing. To investigate this paradox, we recorded the activity of VTA dopamine neurons during a spatial decision-making task. When reward was certain, mice adopted a stereotyped behavior, and dopamine neurons signaled reward. When confronted with uncertain rewards or a novel environment, mice exhibited exploration. Modulation of phasic, but not tonic, dopamine activity predicted uncertainty-seeking and locomotor exploration. Deletion of nAChRs disrupted the influence of uncertainty and novelty on dopamine firing and behavior, sparing reward signaling and learning. Hence, nAChR modulation of dopamine neurons can influence cognitive functions on a short timescale, through the modulation of phasic, synchronous bursting.

neuroscience↗