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Dimitrov, M.

Publications and source records attributed to Dimitrov, M..

2 recordsLinked to original sources

Hippocampal networks support reinforcement learning in partially observable environments

Mastering navigation in environments with limited visibility is crucial for survival. Although the hippocam-pus has been associated with goal-oriented navigation, its role in real-world behaviour remains unclear. To investigate this, we combined deep reinforcement learning (RL) modelling with behavioural and neural data analysis. First, we trained RL agents in partially observable environments using egocentric and allocentric tasks. We show that agents equipped with recurrent hippocampal circuitry, but not purely feedforward networks, learned the tasks in line with animal behaviour. Next, using dimensionality reduction, our agents predicted reward, strategy, and temporal rep-resentations, which we validated experimentally using hippocampal recordings. Moreover, hippocampal RL agents predicted state-specific trajectories, mirroring empirical findings. In contrast, agents trained in fully observable en-vironments failed to capture experimental observations. Finally, we show that hippocampal-like RL agents demon-strated improved generalisation across novel task conditions. In summary, our findings suggest an important role of hippocampal networks in facilitating reinforcement learning in naturalistic environments.

neuroscience↗

Differences in social brain function in autism spectrum disorder are linked to the serotonin transporter

Alterations in the serotonergic control of brain pathways responsible for facial-emotion processing in people with autism spectrum disorder (ASD) may be a target for intervention. However, the molecular underpinnings of autistic-neurotypical serotonergic differences are challenging to access in vivo. Receptor-Enriched Analysis of functional Connectivity by Targets (REACT) has helped define molecular-enriched fMRI brain networks based on a priori information about the spatial distribution of neurochemical systems from available PET templates. Here, we used REACT to estimate the dominant fMRI signal related to the serotonin transporter (5-HTT) distribution during processing of aversive facial expressions of emotion processing in adults with and without ASD. We first predicted a group difference in baseline (placebo) functioning of this system. We next used a single 20 mg oral dose of citalopram, i.e. a serotonin reuptake inhibitor, to test the hypothesis that network activity in people with and without ASD would respond differently to inhibition of 5-HTT. To confirm the specificity of our findings, we also repeated the analysis with 5-HT1A, 5-HT1B, 5-HT2A, and 5-HT4 receptor maps. We found a baseline group difference in the 5-HTT-enriched response to faces in the ventromedial prefrontal cortex. A single oral dose of citalopram shifted the response in the ASD group towards the neurotypical baseline but did not alter response in the control group. Our findings suggest that the 5HTT-enriched functional network is dynamically different in ASD during processing of socially relevant stimuli. Whether this acute neurobiological response to citalopram in ASD translates to a clinical target will be an important next step.

neuroscience↗