Quadriceps weakness is a primary concern following anterior cruciate ligament reconstruction (ACLR), and neuroimaging studies have revealed higher motor inhibition and structural atrophy of the corticospinal tract. To investigate the contributions of supraspinal mechanisms underlying spinal motoneuron impairments and quadriceps weakness, this study explored the firing patterns of motor units (MUs) in the vastus medialis muscle following ACLR. Twenty individuals with primary ACLR and twenty matched controls performed a unilateral knee extension torque-control task at 50% of maximal voluntary effort. High density electromyographic activity of the vastus medialis muscle was decomposed into constituent MU action potentials. Electroencephalography was used to localize cortical activity to sensory and motor brain regions. Active motor thresholds were acquired using transcranial magnetic stimulation. We compared motor unit properties, cortical activity, and corticospinal excitability between groups and limbs using mixed effect models and Cohen's effect sizes. Participants with ACLR had weaker quadriceps compared to contralateral and control limbs. Strength deficits were accompanied by recruitment of larger MUs with lower firing rates in the involved limb. Those with ACLR also had lower corticospinal excitability and lower contralateral hemisphere motor cortex activations during quadriceps contractions. Lower corticospinal excitability and lower activations in the sensory and motor cortices were weakly associated with smaller MU action potential amplitudes, while group was not. Larger, slower-firing quadriceps MUs are recruited at lower absolute and mass-normalized recruitment thresholds, but not relative recruitment thresholds after ACLR. Lower corticospinal excitability and motor cortex activity were associated with recruitment of smaller MUs irrespective of ACLR.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1152/japplphysiol.00641.2024 | DOI Listing |
Brain Commun
February 2025
Division of Neurorehabilitation, Department of Clinical Neurosciences, University Hospitals of Geneva, Geneva 14 1211, Switzerland.
Fatigue is the main cause of disability after traumatic brain injury and has negative impact on social, physical and cognitive functions, participation in daily activities, and ability to work. Since the neural underpinnings are largely unknown, few causal treatments are currently available. This study therefore aimed to investigate the neural correlates of subjective fatigue after traumatic brain injury, controlling for differences in cognitive performance, motor performance and subjective psychological covariates such as depression, anxiety and apathy.
View Article and Find Full Text PDFJ Appl Physiol (1985)
March 2025
Cognition, Neuroplasticity, & Sarcopenia (CNS) Lab, Institute of Exercise Physiology and Rehabilitation Science, University of Central Florida, Orlando, FL, USA.
Quadriceps weakness is a primary concern following anterior cruciate ligament reconstruction (ACLR), and neuroimaging studies have revealed higher motor inhibition and structural atrophy of the corticospinal tract. To investigate the contributions of supraspinal mechanisms underlying spinal motoneuron impairments and quadriceps weakness, this study explored the firing patterns of motor units (MUs) in the vastus medialis muscle following ACLR. Twenty individuals with primary ACLR and twenty matched controls performed a unilateral knee extension torque-control task at 50% of maximal voluntary effort.
View Article and Find Full Text PDFJ Neural Eng
March 2025
Centre for Rehabilitation Engineering, University of Glasgow, James Watt Building (South), G12 8QQ, Glasgow, G12 8QQ, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND.
The study objective was to characterise indices of learning and patterns of connectivity in two neurofeedback (NF) paradigms that modulate mu oscillations in opposite directions, and the relationship with change in excitability of the corticospinal tract (CST). Approach: Forty-three healthy volunteers participated in 3 NF sessions for upregulation (N=24) or downregulation (N=19) of individual alpha (IA) power at central location Cz. Brain signatures from multichannel electroencephalogram (EEG) were analysed, including oscillatory (power, spindles), non-oscillatory components (Hurst exponent), and effective connectivity (Directed Transfer Function) of participants who were successful at enhancing or suppressing IA power at Cz.
View Article and Find Full Text PDFEur J Neurosci
March 2025
School of Health and Rehabilitation Sciences, The University of Queensland, St Lucia, Queensland, Australia.
Transcranial alternating current stimulation (tACS) has been proposed to modulate neural activity through two primary mechanisms: entrainment and neuroplasticity. The current study aimed to probe both of these mechanisms in the context of the sensorimotor μ-rhythm using transcranial magnetic stimulation (TMS) and electroencephalography (EEG) to assess entrainment of corticospinal excitability (CSE) during stimulation (i.e.
View Article and Find Full Text PDFBrain Stimul
March 2025
Department of Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA; Center for Neurological Restoration, Neurological Institute, Cleveland Clinic, Cleveland, OH, USA; Cleveland Clinic Rehabilitation Hospitals, Department of Physical Medicine and Rehabilitation, Cleveland Clinic, Cleveland, OH, USA. Electronic address:
Background: Deep brain stimulation of the dentate nucleus (DN-DBS) is an emerging therapy to improve upper extremity (UE) motor function after stroke. This study sought to investigate the physiologic mechanisms of acute DN-DBS in chronic stroke survivors enrolled in a phase I trial for DN-DBS.
Methods: Twelve chronic stroke participants with moderate-to-severe UE impairment received (acute) single sessions (≥45 min) of active DBS and sham DBS in a sham-controlled, double-blind, cross-over experiment (order randomized).
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!