Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.04.08.717204

Automated Extraction and Meta-Analysis of a Century of Motor-Unit Research with NeuromechaniX

Abstract

The scientific literature on human motor units and electromyography (EMG) spans over a century (1925-2025), comprising research impossible to synthesize manually. We introduce NeuromechaniX, a domain-specific platform for automated extraction and meta-analysis of this literature. The core component, MUscraper, is a large language model pipeline that extracts approximately 200 structured metadata fields, organized into 17 major sections spanning participant demographics, EMG acquisition parameters, muscle identification, task protocols, decomposition methods, and motor-unit outcomes, from [~]2,000 publications on human limb muscles. This automated extraction transforms heterogeneous narrative reports into a standardized, queryable database at a scale not achievable through manual review. From this dataset, we analyzed motor-unit discharge rate across 208 studies examining seven muscles. Our analyses reveal that discharge rates differ significantly among muscles (p<0.001), with biceps brachii exhibiting the highest rates (15.9 pps), followed by first dorsal interosseous (13.7 pps) and tibialis anterior (13.5 pps), whereas gastrocnemius (11.3 pps), the vastii muscles (11.5 pps) and soleus show the lowest rates (9.9 pps). Sex-stratified analysis shows females exhibit higher discharge rates than males (14.5 vs 11.9 pps; Cohens d=0.38, p=0.018). In contrast, age-stratified analysis reveals non-significant differences between young and older adults (d=-0.24, p=0.072). Collectively, these results show that current views of human motor units are limited to a few muscles, with little data on females and older adults. The complete structured database is available through an open-access interactive platform (https://neuro-mechanix.com/metadata), enabling researchers to explore, filter, and download the extracted metadata. NeuromechaniX provides infrastructure for large-scale meta-research, identification of literature gaps, and hypothesis generation for the neuromechanics community.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Del Vecchio, A., Enoka, R. M.. 2026-04-10. Automated Extraction and Meta-Analysis of a Century of Motor-Unit Research with NeuromechaniX. https://doi.org/10.64898/2026.04.08.717204

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

KEEP EXPLORING

Related preprints

Thoracoabdominal pressure transmission during prone and supine cardiopulmonary resuscitation in fresh-frozen human cadavers

Background: Prone cardiopulmonary resuscitation (CPR) may be necessary when turning a prone patient supine would delay chest compressions. Although prone compressions can generate arterial pressures comparable with or greater than supine CPR, the pathway of pressure transmission is uncertain. We examined synchronized intrathoracic, intra-abdominal, and central arterial pressures in both supine and prone positions. Methods: Two thawed fresh-frozen adult cadavers underwent three, 2-minute mechanical CPR trials per position in a counterbalanced crossover sequence. Solid-state catheters recorded pleural, peritoneal, and central arterial pressures simultaneously. Trial-level outcomes included peak pressure, mean pressure, pressure-time area, and the mean peritoneal-to-pleural pressure gradient. Exploratory fixed-effects models included position, cadaver, and their interaction. Results: Prone CPR increased peak intrathoracic pressure by 7.04 mmHg, peak intra-abdominal pressure by 21.69 mmHg, and peak arterial pressure by 15.40 mmHg. Mean intra-abdominal and arterial pressures increased by 16.22 and 9.90 mmHg, respectively. The mean peritoneal-to-pleural gradient reversed direction from -8.46 mmHg supine to 4.85 mmHg prone. Intrathoracic pressure-time area increased 3.4-fold, from 1.62 to 5.46 mmHg{middle dot}s, and arterial pressure-time area increased 2.2-fold, from 2.96 to 6.42 mmHg{middle dot}s. Conclusions: Compared to supine, prone mechanical CPR generated higher arterial pressures and reversed the pressure relationship across the thoracoabdominal boundary in both cadavers. Higher abdominal pressure coincided with a larger intrathoracic pressure-time area, a pattern compatible with reduced caudal pressure dissipation.

physiology↗

Hypothalamic Farnesoid X Receptor deficiency alters energy balance by modulating hepatic glucose production and adipose tissue metabolism through central insulin signaling.

Objectives: The bile acid nuclear receptor Farnesoid X Receptor (FXR, NR1H4) is a major regulator of metabolism and energy homeostasis in peripheral organs. It modulates bile acid, glucose, and lipid metabolism, as well as fat mass and body weight. However, FXR is also expressed in the brain, particularly in the hypothalamus, a key center for the regulation of energy homeostasis. Although one study has demonstrated a role for brain FXR activation in energy balance, its specific hypothalamic role is still unknown. Here, we examined the role of FXR in the mediobasal hypothalamus in the regulation of energy balance. Methods: We used a genetic approach combined with metabolic phenotyping to determine the effect of FXR invalidation in the mediobasal hypothalamus on metabolic parameters involved in the central regulation of energy homeostasis. Results: Our results demonstrate that hypothalamic FXR deficiency induces a positive energy balance, resulting in a reduction in energy expenditure due to alterations in glucose metabolism accompanied by structural changes in white adipose tissues. Conclusion: This study uncovers a previously unrecognized role for hypothalamic FXR in the central homeostatic control of energy balance, providing new insights into its contribution to peripheral glucose metabolism and adipose tissue structural remodeling.

physiology↗

Rad and Phospholamban are Key Drivers of the Ventricular Adrenergic Response and Stress-Induced Arrhythmia

The adrenergic response is a fundamental mechanism that regulates heart rate (chronotropy), cardiac contractility (inotropy) and relaxation (lusitropy). Adrenergic stress is also a recognized trigger of arrhythmia in disease. Yet, our understanding of the underlying molecular basis remains incomplete. Protein kinase A (PKA) and the calcium/calmodulin-dependent kinase II (CaMKII) phosphorylate multiple targets proposed to participate in the adrenergic response, including the GTP-binding protein Rad, phospholamban (PLB) and ryanodine receptor 2 (RyR2). Here we demonstrate that phosphorylation of both Rad and PLB is necessary for inotropy and lusitropy. We show that changes in cardiac contractility and relaxation are primarily dependent on intracellular calcium handling. Finally, we report that Rad and PLB control stress-induced arrhythmogenesis, despite the phosphorylation of other pro-arrhythmic targets. We have identified the essential molecular components of the adrenergic response, resolving a long-standing debate in cardiac excitation-contraction coupling and refining current models of sympathetic regulation in health and disease.

physiology↗