bioRxiv Science⌕ Search
Home/Archive/bioRxiv

bioRxiv · 10.1101/472324

The impact of modern jazz dance on the electrical brain activity

Wind, J.·Schöllhorn, W.
View original source ↗Export metadata ↓

Abstract

Dance as one of the earliest cultural assets of mankind is practised in different cultures, mostly for wellbeing or for treating psycho-physiological disorders like Parkinson, depression, autism. However, the underlying neurophysiological mechanisms are still unclear and only few studies address the effects of particular dance styles. For a first impression, we were interested in the effects of modern jazz dance (MJD) on the brain activation that would contribute to the understanding of these mechanisms. 11 female subjects rehearsed a MJD choreography for three weeks (1h per week) and passed electroencephalographic (EEG) measurements in a crossover-design thereafter. The objectives were to establish the differences between dancing physically and participating just mentally with or without music. Therefore, each subject realized the four following test conditions: dancing physically to and without music, dancing mentally to and without music. Each of the conditions were performed for 15 minutes. Before and after each condition, the EEG activities were recorded under resting conditions (2 min. eyes-open, 2 min. eyes-closed) followed by a subsequent wash-out phase of 10 minutes.\n\nThe results of the study revealed no time effects for the mental dancing conditions, either to or without music. An increased electrical brain activation was followed by the physical dancing conditions with and without music for the theta, alpha-1, alpha-2, beta and gamma frequency band across the entire scalp. Especially the higher frequencies (alpha-2, beta, gamma) showed increased brain activation across all brain areas. Higher brain activities for the physical dancing conditions were identified in comparison to the mental dancing condition. No statistically significant differences could be found as to dancing to or without music. Our findings demonstrate evidence for the immediate influence of modern jazz dance and its sweeping effects on all brain areas for all measured frequency bands, when dancing physically. In comparison, dancing just mentally does not result in similar effects.

Source connections

Explore related subjects

neurosciencePreprint

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Wind, J., Schöllhorn, W.. 2018-11-16. The impact of modern jazz dance on the electrical brain activity. https://doi.org/10.1101/472324

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

KEEP EXPLORING

Related preprints

bioRxiv2026

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↗
bioRxiv2026

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↗
bioRxiv2026

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↗