Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.11.25.690375

Evidence for separate processes underlying movement and decision vigor in a reward-oriented task

Abstract

The vigor of movement and decision-making is fundamental to many reward-oriented behaviors. While some theories propose that movement and decision are jointly invigorated to maximize a global utility (e.g., mixing reward, effort, and time), alternative perspectives suggest that the brain can separately invigorate them when advantageous. We tested these competing hypotheses using a foraging-like task that allowed experimentally assessing the vigor of movement (reaching to reward location) and that of decision-making (harvesting reward). By using a block-wise design, we measured the effects of independent manipulations of time and effort on reach and harvest durations. Decoupled effects were found on reach and harvest durations, with no inter-individual consistency between them. A model allowing separate, yet inter-dependent, optimizations of movement and decision vigor based on distinct time costs sensitive to recent temporal history predicted these results more accurately than a global utility model. These findings indicate that movement and decision vigor may flexibly depend on whether shared versus distinct time costs underlie behavior; co-regulation would arise when the vigor of movement and decision is governed by a shared time cost but decoupling may emerge when relevant for the task. Significance statementCoordinating movement and decision-making is fundamental to many reward-oriented behaviors. Current theories suggest that the brain may invigorate behavior by co-regulating movement and decision, but some experimental findings rather point to a decoupling. To shed new light on this debate, we developed a foraging-like task promoting independent and comparable manipulation of time and effort. We show that movement and decision are mostly decoupled in this task, invigorated by distinct time-cost signals. Previously experienced delays tend to amplify these time costs, thereby exerting a strong influence on behavior and indirectly linking movement and decision. Co-regulation or decoupling may hinge on whether movement and decision vigor relies on shared or distinct time-cost signals.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Conessa, A., Boutin, A., Berret, B.. 2025-11-28. Evidence for separate processes underlying movement and decision vigor in a reward-oriented task. https://doi.org/10.1101/2025.11.25.690375

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

The Unreasonable Effectiveness of Cell Types in Describing Neuronal Physiological Features

Single-cell RNA sequencing (scRNA-seq) captures detailed gene expression profiles at scale, while patch-clamp recordings measure intrinsic neuronal electrophysiological properties. Modeling the relations between these two modalities remains a challenge. Here, we compare how well electrophysiological features can be predicted by traditional transcriptomic cell type classification, representations derived from a foundational model (scGPT) pretrained on large-scale scRNA-seq datasets, ion channel-coding genes, and highly variable genes. Using paired transcriptomic and electrophysiological patch-sequencing data from 495 human neurons from neurosurgical tissue, we find that cluster-level cell type representations consistently outperform highly variable gene selection, ion channel gene selection, and context-enriched scGPT embeddings. Notably, performance varies across model architectures and initializations, and the best results are obtained by combining the outputs of separate cell type and scGPT-based models. Together, these findings suggest that traditional discrete cellular classification is highly effective in predicting physiological features. For maximum performance it can be complemented by pretrained transformer models.

neuroscience↗

A nonlinear inhibition pathway underlying cortical responses to tuned holographic optogenetic perturbations

Optogenetics enables causal manipulation of cortical activity. Perturbation responses can be counterintuitive due to network interactions, making theory essential for predicting them. Existing approaches often rely on linear approximations, which fail for many biologically relevant perturbations. Here we develop a nonlinear theory of responses to holographic perturbations in cell-type-specific recurrent networks with structured connectivity. We fit a nonlinear model to mouse V1 data, which shows cotuned-ensemble suppression: perturbing spatially clustered neurons with similar preferred orientations yields markedly stronger short-range suppression than perturbing untuned ensembles. We show that cotuned-ensemble suppression arises from a feature-tuned, nonlinear inhibition pathway implicating somatostatin-positive (SST) interneurons. The theory predicts that cotuned ensembles suppress parvalbumin-positive (PV) neurons but facilitate SST neurons, and links the degree of cotuned-ensemble suppression or facilitation to the variance of the SST response. This framework identifies mechanisms by which nonlinear inhibition sculpts cortical dynamics and establishes a predictive basis for targeted optogenetic interventions.

neuroscience↗

Proteomic signatures of APOE ε4 across human tissues and cell types in Alzheimers disease

The apolipoprotein E {varepsilon}4 (APOE {varepsilon}4) allele is the strongest genetic risk factor for late-onset Alzheimers disease (AD). However, the underlying molecular mechanisms remain unclear. This study included 1691 participants from the Religious Orders Study and Rush Memory and Aging Project (ROSMAP), 1226 participants from the Accelerating Medicines Partnership - Alzheimers Disease (AMP-AD) Diverse Cohorts Study, and 735 participants from the Alzheimers Disease Neuroimaging Initiative (ADNI). To characterise APOE {varepsilon}4 molecular effects, we analysed proteomic data from plasma, cerebrospinal fluid (CSF), and induced pluripotent stem cell (iPSC)-derived astrocytes and neurons, as well as transcriptomic and proteomic data from multiple brain regions. The association of APOE {varepsilon}4 with AD neuropathology was also examined. APOE {varepsilon}4 carriers shared a plasma proteomic signature enriched for immune processes, irrespective of AD diagnosis. A machine learning classifier trained on this signature discriminated APOE {varepsilon}4 carriers from non-carriers in an independent cohort using CSF proteomics. APOE {varepsilon}4 carriage was associated with higher Braak stages and Consortium to Establish a Registry for Alzheimers Disease (CERAD) score. However, only limited APOE {varepsilon}4-associated transcriptomic and proteomic changes were observed in bulk brain tissue, with poor cross-layer concordance. Proteomic analyses of iPSC-derived astrocytes and neurons further revealed cell-type-specific APOE {varepsilon}4-associated changes. APOE {varepsilon}4 is associated with a consistent proteomic signature across plasma and CSF. Its molecular effects in the brain differ across cell types, brain regions and molecular layers. These findings support the need for cell-type-resolved multi-omic studies to elucidate how APOE {varepsilon}4 confers AD risk.

neuroscience↗