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During walking and running, animals display rich and coordinated motor patterns that are generated and controlled within the central nervous system. Previous computational and experimental results suggest that the balance between excitation and inhibition in neural circuits may be critical for generating such structured motor patterns. In this paper, we explore the influence of this balance on the ability of a reservoir computing artificial neural network to learn human locomotor patterns, using mean-field theory and simulations. We created networks with varying neuron numbers, connection percentages and connection strengths for the excitatory and inhibitory neuron populations, and introduced the anatomical imbalance that quantifies the overall effect of the two populations. We trained the networks to reproduce muscle activation patterns derived from human recordings and evaluated their performance. Our results indicate that network dynamics and performance depend critically on the anatomical imbalance in the network. Excitation-dominated networks lead to saturated firing rates, thereby reducing the firing rate heterogeneity and leading to muscle coactivation and inflexible motor patterns. Inhibition-dominated networks, on the other hand, perform well, displaying balanced input to the neurons and sufficient heterogeneity in the neuron firing rate patterns. This suggests that motor pattern generation may be robust to increased inhibition but not increased excitation in neural networks.
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http://dx.doi.org/10.1007/s00422-025-01011-7 | DOI Listing |
Amyotroph Lateral Scler Frontotemporal Degener
September 2025
Faculdade de Medicina, Centro de Estudos Egas Moniz, Universidade de Lisboa, Lisboa, Portugal.
This study aimed to derive standardized regression-based (SRB) reliable change indices (RCIs) for the cognitive section of the Portuguese Edinburgh Cognitive and Behavioral ALS Screen (ECAS-C). Forty-nine MND patients undergoing the ECAS were followed-up (T1) at 7.2 ± 2 months (range = 5-12).
View Article and Find Full Text PDFNeurosci Bull
September 2025
Zhejiang Key Laboratory of Organ Development and Regeneration, College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, 311121, China.
The neurological manifestations of SHORT syndrome include intrauterine growth restriction, microcephaly, intellectual disability, hearing loss, and speech delay. SHORT syndrome is generally believed to be caused by PIK3R1 gene mutations and impaired PI3K-AKT activation. Recently, a clinical case report described a SHORT syndrome with a novel mutant in PRKCE gene encoding protein kinase Cε (PKCε).
View Article and Find Full Text PDFNeurosci Biobehav Rev
September 2025
Department of Psychiatry, The University of Melbourne, Melbourne, Victoria, Australia; Department of Psychiatry, The University of Melbourne, Austin Health, Melbourne, Victoria, Australia. Electronic address:
One of the characteristic presentations of functional neurological disorder (FND) is with motor symptoms, such as weakness and tremor. While these symptoms are both common and disabling, how they arise at a mechanistic level remains unclear. This review provides an up-to-date account of the underpinnings of motor dysfunction in FND by integrating findings from neuroimaging, physiology, genetic, brain stimulation, and behavioral studies.
View Article and Find Full Text PDFBrain Stimul
September 2025
Department of Philosophy, University of Milan, Milan, via Festa Del Perdono, 7, 20122, Italy; Cognition in Action (CIA) Unit, PHILAB, University of Milan, Via Santa Sofia, 9, 20122, Italy. Electronic address:
Background: To investigate covert motor processes, transcranial magnetic stimulation (TMS) studies often use motor-evoked potentials (MEPs) as a proxy for inferring the state of motor representations. Typically, these studies test motor representations of actions that can be produced by the isolated contraction of one muscle, limiting both the number of recorded muscles and the complexity of tested actions. Furthermore, univariate analyses treat MEPs from different muscles as independent, overlooking potentially meaningful intermuscular relationships encoded in MEPs amplitude patterns at the single-trial level.
View Article and Find Full Text PDFParkinsonism Relat Disord
September 2025
Federal University of São Paulo, Department of Neurology and Neurosurgery, São Paulo, SP, Brazil.
Background: Huntington disease-like 2 (HDL2) is an autosomal dominant disorder caused by an abnormal CAG/CTG repeat in exon 2A of junctophilin-3. This is the most common Huntington's Disease phenocopy and is characterized by psychiatric, cognitive, and movement disorders. This study aimed to describe the clinical phenotype of HDL2 patients in Brazil and compare the findings with those in the literature.
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