Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.07.22.666199

Non-invasive Stimulation of Contralateral Primary Motor Cortex Reduces the Amount of Skill Generalization to the Untrained Arm

Abstract

Successfully learned motor skills can generalize or transfer to the untrained arm. The neural substrate underlying such intermanual/interlimb generalization of newly acquired skill memory is unclear. Here, we focused on contralateral primary motor cortex (cM1) which is considered a key brain area for skill learning and memory consolidation. We probed the causal role of cM1 in intermanual skill generalization in a two-day study involving right-handed young individuals (n=31) who learned a novel motor skill reaching task. Immediately following (right-arm) learning, we delivered low-frequency (1Hz, 1800 pulses) repetitive transcranial magnetic stimulation (rTMS) to target left cM1 in one group of individuals (n=15), while another group (n=16) served as an active control in which ipsilateral M1 (iM1) was targeted. On the same day we measured corticospinal excitability (CSE) to assess learning-induced and rTMS-induced neuroplastic changes occurring in the targeted M1s. Next day after 24-hours, both groups were tested for intermanual skill generalization (left-arm), followed by a brief test of intralimb retention (right-arm). Our results show that stimulating cM1, versus iM1, reduced the amount of generalization to the untrained arm on the next day, without affecting its (re)learning ability or the follow-up retention performance of the trained arm. Further, rTMS stimulation induced a net facilitation in CSE- with higher facilitation tending to correlate to lower generalization in a subset of high learners in cM1 group. Taken together, this study highlights the role of cM1 in skill generalization such that it seems to mediate the early transfer of learning to the untrained arm. NEW AND NOTEWORTHYIntermanual skill generalization from trained to the untrained arm is causally mediated by the contralateral (trained) primary motor cortex (cM1) as opposed to the ipsilateral (untrained) motor cortex. Low-frequency stimulation of M1 in our study led to a facilitation of corticospinal excitability, while impairing the amount of skill generalization in the cM1 group. This highlights a rather paradoxical and opposite effect of non-invasive brain stimulation, such as rTMS, on motor behavior and associated motor excitability. Our data also suggest involvement of additional brain areas for such motor skill behavior that were rendered unperturbed by rTMS in this case and, thus, contributed to an overall positive skill performance achieved by both arms the next day.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Yadav, G., Chauvaux, M., Duque, J.. 2025-07-26. Non-invasive Stimulation of Contralateral Primary Motor Cortex Reduces the Amount of Skill Generalization to the Untrained Arm. https://doi.org/10.1101/2025.07.22.666199

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

KEEP EXPLORING

Related preprints

Connexin 40 deficiency alters the temporal profile of postictal oxygen dynamics following focal seizures.

Epilepsy is increasingly recognized as a disorder involving both neuronal and vascular dysfunction. While connexin signaling has been implicated in epileptogenesis, the contribution of vascular connexins to seizure associated cerebrovascular pathology remains poorly understood. Connexin40 (Cx40) is an endothelial gap junction protein that plays a crucial role in vascular communication and blood-flow regulation. Seizures induce dynamic changes in cerebral perfusion and oxygenation, including prolonged postictal hypoperfusion/hypoxia. To determine whether Cx40 influences postictal hypoxia following focal seizures, we examined seizure characteristics and postictal oxygen dynamics in Cx40 knockout (Cx40-/-) mice using an established focal hippocampal seizure model. Electrically kindled seizures were elicited in wild-type and Cx40-/- mice, and local hippocampal tissue oxygenation was continuously monitored before and after seizure induction. Seizure duration did not differ between genotypes, indicating comparable seizure severity. Interestingly, Cx40 deletion altered the temporal pattern of postictal oxygen recovery, producing greater early hypoxia and a delayed secondary rebound in pO2 despite similar peak oxygen levels and overall hypoxic burden. These findings demonstrate that loss of Cx40 selectively alters the temporal profile of postictal oxygen dynamics without affecting seizure duration. Taken together, the results suggest that endothelial gap junctional communication contributes to postictal vascular recovery and identify Cx40 as a potential modulator of seizure associated neurovascular dysfunction.

neuroscience↗

Attention Across Scales: From Individual Variation to Social Hierarchies and Brain Networks in Semi-Free-Ranging Macaques

Attention is a fundamental brain function supporting perception, decision-making, and social behavior, and its dysfunction profoundly impairs daily life. It is both dynamic and stable, varying across observations and individuals, changing across the lifespan, and being shaped by social and environmental experience. Yet capturing this complexity remains a central challenge in neuroscience. Here, we integrated longitudinal behavioral assessments of semi-free-ranging macaques living in naturalistic social groups with resting-state fMRI. We quantified performance across days, ages, and social hierarchies and related it to intrinsic brain organization. Distinct attentional phenotypes emerged, including individuals with reduced attentional control. Performance followed an inverted-U lifespan trajectory, improving from childhood to adulthood before declining. Social status modulated attentional performance. Critically, nonlinear lifespan trajectories and associations with individual attentional differences were most clearly expressed in frontoparietal connectivity. Together, these findings reveal how sustained attention is organized across scales, providing a biological framework for its individual diversity, social modulation, and neural basis.

neuroscience↗

Decoding natural scenes from patterned optogenetic responses in mouse visual cortex

A central challenge in developing visual cortical prostheses is to determine how visual stimuli should be transformed into effective patterns of cortical stimulation. Although advances in stimulation technologies, including optogenetics, provide increasingly precise control over cortical activity, it remains unclear whether artificially evoked activity can reproduce the information content of naturally evoked visual representations. Here we establish a quantitative framework for evaluating visual encoding strategies by decoding cortical responses evoked by natural vision and patterned optogenetic stimulation. We developed a novel dual-modal paradigm in awake mice to bridge the gap between endogenous photostimulation and artificial network driving. By co-expressing the high-performance calcium indicator GCaMP6s and the red-shifted, ultra-sensitive opsin rsChRmine-oScarlet in the primary visual cortex (V1), we successfully translated dynamic natural movie frames into patterned, spatiotemporal optogenetic stimulation. Quantitative comparisons of macro-scale dynamics demonstrated that this patterned optogenetic injection evokes cortical states highly comparable and representationally aligned with those driven by actual visual photostimulation. To systematically evaluate the fidelity of these responses, we developed STAR, a deep learning model featuring spatial and temporal attention mechanisms, and successfully reconstructed the frames of natural movies from V1 signals under both experimental modalities. Collectively, our results demonstrate that complex sensory information can be both naturally encoded and synthetically injected into V1 circuits with high decoding fidelity. This work provides an empirical and computational proof-of-concept for intelligent, closed-loop biomimetic encoders, establishing a robust framework for next-generation cortical visual neuroprostheses and bidirectional brain-machine interfaces.

neuroscience↗