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Svoboda, J.

Publications and source records attributed to Svoboda, J..

6 recordsLinked to original sources

Domain Adaptation Enables Cross-site Classification of First-episode Schizophrenia from Multimodal Neuroimaging Data

Identifying robust neuroimaging markers associated with schizophrenia is essential for advancing research and informing clinical understanding. However, a major obstacle to clinical translation is the limited ability of neuroimaging-based classification models to generalise across scanning sites. In this study, we first establish best performing within-site models, and then systematically investigate cross-site generalisation in first-episode schizophrenia (FES) classification and evaluate strategies for mitigating site-related distribution shifts. Using data from two acquisition sites (n = 389 in total), we perform train-on-site/test-on-site experiments to analyze performance degradation under domain shift and examine the effectiveness of ComBat, optimal transport, and adversarial adaptation strategies. Across functional, structural, and diffusion-based features, both traditional machine learning (TML) and neural network (NN) models achieve comparable performance in within-site classification, with resting state fMRI functional connectivity providing the most robust unimodal features. When models are transferred across sites, performance degrades substantially across all approaches, highlighting the impact of site-related variability. Distribution-alignment methods partially mitigate this degradation, with ComBat and optimal transport yielding more consistent cross-site improvements than adversarial adaptation. Increasing model complexity alone does not result in systematic performance gains, and simple models combined with effective alignment strategies often perform comparably to more complex neural architectures, while multimodal feature fusion does not consistently outperform functional connectivity alone. Overall, our findings indicate that controlling for site effects is more critical than model complexity for achieving generalisable classification in FES, underscoring the importance of rigorous evaluation designs and explicit distribution-alignment strategies for neuroimaging-based predictive models with potential clinical utility.

neuroscience↗

Chondroitin 4-sulphate depletion enhances synaptic plasticity and memory in aging

Perineuronal nets (PNNs), specialised extracellular matrix structures enriched in chondroitin sulphate proteoglycans (CSPGs), are key regulators of synaptic plasticity, learning, and memory. Aging is characterised by a shift in chondroitin sulphate composition toward increased chondroitin-4-sulfation (C4S) and reduced C6S, a pattern associated with declining cognitive flexibility. Here, we investigated how selective reduction of C4S affects PNN structure, PV-interneuron connectivity, and cognitive performance across the lifespan. Conditional deletion of the C4-sulfotransferase Chst11 markedly reduced C4S levels and diminished dendritic PNN complexity while preserving somatic PNN structure. This partial destabilisation of PNNs increased excitatory synaptic input onto PV interneurons in both young and aged mice, without major alterations in basal hippocampal transmission or long-term potentiation. Behaviourally, Chst11 knockout mice showed robust and persistent protection against age-related cognitive decline. Working memory performance remained stable across aging, short-term spatial memory was enhanced from early adulthood onward, and object recognition memory was significantly prolonged at all retention delays, even in old age. Sociability and social novelty preference were also preserved longer in aging knockouts compared with controls. These improvements occurred despite an overall preservation of PNN architecture, indicating that modifying sulphation rather than removing CSPGs is sufficient to enhance plasticity. Our findings demonstrate that reducing C4S through Chst11 deletion confers long-lasting enhancements in cognitive function and mitigates aging-related decline. Targeting CS-GAG sulphation patterns may therefore represent a promising strategy for maintaining cognitive resilience and restoring plasticity in aging or neurodegenerative conditions.

neuroscience↗

CA1 ensemble plasticity is coupled to context change and modulated by task familiarity

When should plasticity mechanisms get recruited (stability-plasticity dilemma)? Environments change over time, re/entering a given context increases uncertainty and predicts the need for updating. Hippocampus (HPC) is key to tracking context change but also navigation in relation to moving targets. CA1 ensembles expressing immediate-early genes (IEGs) are contextually specific, while the amount of IEG expression correlates with HPC-dependent task demands. However, task effects on the IEG-expressing ensembles per se remain unclear. In three experiments, we tested the effect of context change and HPC task demands on CA1 IEG+ ensembles in rats. Experiment 1 showed that the IEG+ (Arc, Homer1a RNA) ensemble size drops to baseline level during uninterrupted 30 min exploration, reflecting familiarization and decreasing uncertainty, unless context change is present; the ensemble sizes reflect both context identity and context change. Experiment 2 showed no evidence of task-specificity of IEG+ ensembles during highly HPC-dependent mobile robot avoidance nor HPC-independent stationary robot avoidance. Experiment 3 replicated the findings of Experiment 2 for c-Fos protein. Nonetheless, the data suggest that ensembles shrink with task mastery/familiarity and grow with novelty presented by acquisition of behavioral extinction. Overall, our results shed light on the temporal dynamics, and the context and task control of CA1 IEG+ ensembles. The present results and the relevant literature suggest that context change resets the ensemble of IEG-expressing CA1 neurons and novelty delays the time-dependent ensemble shrinking. HIGHLIGHTSO_LIPlasticity and learning rate should reflect novelty and familiarity, i.e. uncertainty C_LIO_LIChange of context and task requirements increase uncertainty C_LIO_LIFamiliarization with context and task reduces uncertainty C_LIO_LIFor context, this pattern is matched by dynamics of IEG+ ensembles in CA1 C_LIO_LITask demands have modulating influence on CA1 IEG+ ensembles C_LI GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=140 SRC="FIGDIR/small/608588v1_ufig1.gif" ALT="Figure 1"> View larger version (26K): org.highwire.dtl.DTLVardef@12808c0org.highwire.dtl.DTLVardef@156ad3corg.highwire.dtl.DTLVardef@1876f0aorg.highwire.dtl.DTLVardef@8b13f4_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗

PV+ optogenetic stimulations at specific frequencies in specific brain regions can restore navigational flexibility in an acute MK801 mouse model of schizophrenia

Impairments of decision-making and behavioral flexibility in schizophrenia (SCZ) are currently the most investigated features. One convincing hypothesis explaining this cognitive impairment is the excitatory/inhibitory (E/I) ratio imbalance in brain regions such as the medial prefrontal cortex (mPFC) and the ventral hippocampus (vHPC). An increased GLUergic excitatory activity and a decreased GABAergic inhibitory activity induces an mPFC-vHPC {gamma}/{theta} band desynchronization in many tasks testing behavioral flexibility. However, these tasks were carried out using "perceptual" decision-making/flexibility but not navigational decision-making/flexibility. Our study addressed the role of frequency-specific optogenetic stimulations of GABAergic parvalbumin-positive (PV+) interneurons in mPFC (50Hz, {gamma}-like) and vHPC (10Hz, {theta}-like) in an acute-MK801 mouse model of navigational inflexibility. We used the active place avoidance task on a rotating arena. Results showed that frequency-specific optogenetic stimulations of mPFC or vHPC acted differently in restoring navigational flexibility, advancing our knowledge of the pivotal role of PV+ activity in SCZ-like navigational decision-making/flexibility.

animal behavior and cognition↗

Incidental Temporal Binding in Rats: A Novel Behavioral Task Relevant to Episodic Memory

We designed a behavioral task called One-Trial Trace Escape Reaction (OTTER), in which rats incidentally associate two temporally discontinuous stimuli: a neutral acoustic cue (CS) with an aversive stimulus (US) which occurs two seconds later (CS-2s-US sequence). Rats are first habituated to two similar environmental contexts (A and B), each consisting of an interconnected dark and light chamber. Next, rats experience the CS-2s-US sequence in the dark chamber of one of the contexts (either A or B); the US is terminated immediately after a rat escapes into the light chamber. The CS-2s-US sequence is presented only once to ensure the incidental acquisition of the association. The recall is tested 24 h later when rats are presented with only the CS in the alternate context (B or A), and their behavioral response is observed. Our results show that 59 % of the rats responded to the CS by escaping to the light chamber, although they experienced only one CS-2s-US pairing. The OTTER task offers a flexible high throughput tool to study memory acquired incidentally after a single experience. Incidental acquisition of association between temporally discontinuous events is highly relevant to episodic memory formation.

animal behavior and cognition↗

The role of optogenetic stimulations of parvalbumin-positive interneurons in the prefrontal cortex and the ventral hippocampus on an acute MK801 model of schizophrenia-like cognitive inflexibility

Background and HypothesisSchizophrenia research arose in the last decades, focusing more on its neural basis. Executive functions such as decision making and cognitive flexibility are the main cognitive areas that are impaired and are considered schizophrenia endophenotypes. Recently, cognitive impairment has been connected with the ablation of glutamatergic NMDARs resulting in increased cortical activity. Selective NMDARs antagonists such as dizocilpine have been used to model cognitive inflexibility in schizophrenia. Moreover, a decreased GABAergic inhibitory activity has been shown elsewhere along with the enhanced cortical activity. This NMDARs/GABA unbalanced ratio may reduce the entrainment of prefrontal gamma and hippocampal theta rhythm, resulting in a prefrontal-hippocampal gamma/theta band desynchronization. Study DesignThe study addressed the role of acute administrations of dizocilpine to model schizophrenia-like cognitive inflexibility in rats. We used a new version of the attentional set-shifting task, where rats learned switching/reversing the relevant rule. Moreover, we used the new ASST after dizocilpine systemic injections to test cognitive flexibility. Finally, we used in vivo optogenetic stimulations at specific light pulses of parvalbumin-positive interneurons in the prefrontal cortex and ventral hippocampus. ResultsThe first experiments showed that acute dizocilpine in rats reproduced schizophrenia-like cognitive inflexibility. The second set of experiments demonstrated that appropriate optogenetic light pulses frequencies could rescue the cognitive flexibility previously altered by acute dizocilpine. ConclusionsThese findings advance our knowledge on the pivotal role of parvalbumin interneurons in schizophrenia-like cognitive impairment and may serve as a standpoint for further research of this severe psychiatric disorder.

neuroscience↗