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Pascual Valdunciel, A.

Publications and source records attributed to Pascual Valdunciel, A..

4 recordsLinked to original sources

Neurofeedback Training on Motor Cancellation Enhances Peripheral but not Cortical Beta Band Oscillations

Beta oscillations (13-30 Hz) are a prominent sensorimotor neural rhythm and an important biomarker in neurorehabilitation. These oscillations propagate along the corticospinal pathway and are expressed in the discharge patterns of spinal motor neurons, enabling the assessment of corticomuscular coupling. Moreover, peripheral beta band oscillations have recently emerged as a potential control signal for motor augmentation interfaces. However, it remains unclear whether peripheral beta activity simply reflects cortical oscillations or is partly shaped by peripheral mechanisms, and to what extent it can be voluntarily controlled. To address these questions, we developed a 10-day neurofeedback protocol in which participants learned to up-regulate peripheral beta band activity. Subjects were trained to exploit movement cancellation, a behaviour naturally associated with increased cortical and muscle beta band activity, as a two-state strategy to voluntarily modulate peripheral beta band power. Each session included a guided familiarization phase based on a GO/NO-GO task, in which participants familiarized with movement cancellation through guided visual cues, followed by an asynchronous control phase in which they self-initiated the same strategy without external guidance to increase peripheral beta band activity in a target window. Participants progressively improved their ability to voluntarily modulate peripheral beta band activity. Peripheral beta band power during movement cancellation increased significantly across training days in both the familiarization and asynchronous control phases. Intramuscular coherence in the beta band also increased, indicating enhanced common synaptic input to the motor neuron pool in this band. In contrast, cortical beta power and corticomuscular coherence remained unchanged. Together, these findings demonstrate that peripheral beta band activity is a dynamic neural feature that can be voluntarily shaped through training, supporting its potential as a non-invasive control signal for future neurorehabilitation and motor augmentation technologies.

bioengineering↗

High-frequency common inputs entrain motoneuron subpopulations differently

Spinal motoneuron (MN) pools behave as linear systems that transmit common synaptic input to muscles. However, MNs are biophysically heterogeneous and intrinsically nonlinear. How different MN subpopulations integrate and transmit high-frequency inputs remains poorly understood, partly because conventional analyses treat the MN pool as a single functional system rather than examining subpools with different firing rates. Here, we addressed this gap using a combination of computational simulations and human MN recordings. Simulations of MNs receiving a common synaptic input at varying frequencies showed that MNs firings become phase-locked to input oscillations when the input frequency approximates the neurons firing rate or its harmonics. We refer to this frequency-dependent synchronization as entrainment. Importantly, this subpool-specific effect was masked when MN activity was analysed at the whole-pool level. Because entrained MNs effectively sample the input at their firing instants, we developed a MN-firing locked method that uses individual MN firings as endogenous triggering events for peristimulus frequencygrams across the pool. In simulations, this method revealed entrainment-driven firing rate modulations across MN subpools. We then applied this MN-firing locked method to MNs decomposed from high-density surface electromyography recordings obtained during isometric contractions in healthy individuals. We found that faster-firing MNs exhibited larger transient firing rate increases, time-locked to slower MN activity. Furthermore, these modulations correlated with common input in the alpha and beta bands implicating high frequency common input as the driving source. Together, these findings demonstrate that MN nonlinearities generate heterogeneous, frequency-dependent dynamics that remain hidden in conventional pool-level analyses.

neuroscience↗

TMS-Evoked Corticospinal Beta Oscillations in Humans Recorded from Muscles

BackgroundTranscranial magnetic stimulation (TMS) can entrain oscillatory brain activity, offering a promising approach to study motor-related neural oscillations such as beta rhythms. However, how TMS-induced corticospinal oscillations are generated, propagated, and related to endogenous activity remains unclear, partly due to limitations in brain recording techniques. Recording muscle activity provides an alternative and physiologically grounded window into corticospinal dynamics. MethodsWe investigated whether subthreshold TMS over the motor cortex induces corticospinal oscillatory activity detectable in muscles, and whether these responses share neural generators with endogenous beta rhythms. Single-pulse subthreshold TMS was applied over the motor cortex in healthy participants while electromyography (EMG) was recorded from tonically active muscles. Stimulation intensity, coil orientation, and stimulation site were systematically varied. Concurrent electroencephalography (EEG) was used to assess cortical responses and corticomuscular transmission. In additional experiments, advanced EMG techniques were employed to track motor neuron pools and characterize how TMS-evoked oscillations are transmitted at the motor unit level. ResultsTMS elicited a robust and short-latency increase in beta-band activity in the EMG. The analysis of the elicited muscle responses and the comparison of results across different TMS configurations indicate that the beta responses resulted from activation of inhibitory interneurons in the targeted primary motor cortex. Importantly, the characteristics of cortico-muscular coherence and beta projection to the muscles indicate that the elicited beta responses with TMS have same cortical sources as endogenously generated beta activity. ConclusionsThese findings demonstrate that muscle recordings provide a sensitive and physiologically meaningful readout of TMS-induced corticospinal beta oscillations.

neuroscience↗

Modulation of spinal circuits following phase-dependent electrical stimulation of afferent pathways

Peripheral electrical stimulation (PES) of afferent pathways is a tool commonly used to induce neural adaptations in some neural disorders such as pathological tremor or stroke. However, the neuromodulatory effects of stimulation interventions synchronized with physiological activity (closed-loop strategies) have been scarcely researched in the upper-limb. Here, the short-term spinal effects of a 20-minute stimulation of afferent pathways protocol applied with a closed-loop strategy named Selective and Adaptive Timely Stimulation (SATS) was explored. The SATS strategy was applied to the radial nerve in-phase (INP) or out-of-phase (OOP) with respect to the muscle activity of the extensor carpi radialis (ECR). The neural adaptations at the spinal cord level were assessed for the flexor carpi radialis (FCR) by measuring disynaptic Group I inhibition, Ia presynaptic inhibition, and Ib facilitation from the H-reflex, and estimation of the neural drive before, immediately after, and 30 minutes after the intervention. SATS strategy was proved to deliver synchronous stimulation with the real-time measured muscle activity with an average delay of 17{+/-}8 ms. SATS-INP induced an increase of the disynaptic Group I inhibition (77{+/-}23 % of baseline conditioned FCR H-reflex), while SATS-OOP elicited the opposite effect (125{+/-}46 %). Not all the subjects maintained the changes after 30 minutes. Additionally, no other significant specific neural adaptations were found for the rest of measurements. These results suggest that the short-term modulatory effects of phase-dependent PES occur at the specific targeted spinal pathways for the wrist muscles in healthy individuals. Overall, timely recruitment of afferent pathways with the muscle activity is a fundamental principle which should be considered in tailoring PES protocols for the specific neural circuits to be modulated.

neuroscience↗