bioRxiv Science⌕ Search

bioRxiv · 10.1101/2021.09.07.459353

Concurrent Multimodal Data Acquisition During Brain Scanning is within Reach

Abstract

BackgroundPrevious brain-scanning research exploring the neural mechanisms underpinning visuomotor planning and control has mostly been done without simultaneous motion-tracking and eye-tracking. Employing concurrent methodologies would enhance understanding of the brain mechanisms underlying visuomotor integration of cognitive, visual, ocular, and motor aspects of reaching and grasping behaviours. Therefore, this work presents the methods and validation for a high-speed, multimodal and synchronized system to holistically examine neural processes that are involved in visually-guided movement. MethodsThe multimodal methods included high speed 3D motion tracking (Qualisys), 2D eye-tracking (SR Research), and magnetoencephalography (MEG; Elekta) that were synchronized to millisecond precision. Previous MRIs were taken to provide improved spatial localization. The methods section describes the system layout and acquisition parameters to achieve multimodal synchronization. Pilot results presented here are preliminary data from a larger study including 29 participants. Using a pincer grip, five people (3 male, 2 female, ages 30-32) reached for and grasped a translucent dowel 50 times, after it was pseudorandomly illuminated. The object illumination was the Go cue. Seven discrete time points (events) throughout the task were chosen for investigation of simultaneous brain, hand and eye activity associated with specific visual (Go cue), oculomotor (1st saccade after Go), motor (Reaction Time; RT, Maximum Velocity: MV, Maximum Grip Width; MGW) or cognitive (Ready, End) mechanisms. Time-frequency analyses were performed on the MEG data sourced from the left precentral gyrus to explore task-related changes time-locked to these chosen events. Pilot resultsBasic kinematic parameters including RT, MV, MGW, Movement Time, and Total Time were similar to previous, seminal research by Castiello, Paulignan and Jeannerod, (1991), using a similar task. Although no gaze instructions were given, eye-tracking results indicated volunteers mostly gazed at or near the target object when Ready (72%), and then hardly looked away throughout the rest of the task at the important events sampled here (92% - 98%). At the End event, when lifting the dowel, on average, participants gazed at or near the target object 100% of the time. Although saccades > 100 ms after Go, but prior to RT were made on average in about one fourth (M = 13, SD = 6) of trials, a mixed model (REML) indicated their latency in timing after the Go was significantly (F = 13.376, p = .001) associated with RT scores on those trials (AIC = 724, R m2 = 0.407, Rc2= 0.420). Neural activity relative to baseline in the beta band was desynchronized for the visually guided reach periods, beginning prior to Go, and remaining sustained until beyond End, after the grasp and lift were executed. ConclusionThis study presents the layout, acquisition parameters and validation for a multimodal, synchronized system designed to record data from the hand, eye and brain simultaneously, with millisecond precision during an ecologically-valid prehension task with physical, 3D objects. The pilot results align with previous research made with single or bimodal data recordings. This multimodal method enables full-brain modelling that can holistically map the precise location and timing of neural activity involved in the visual, oculomotor, motor and cognitive aspects of reach-to-grasp planning and control.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Sola Molina, R. M., Lamp, G., Hugrass, L. E., Beaton, R., De Man, M., Wise, L., Crewther, D. P., Goodale, M., Crewther, S. G.. 2021-09-09. Concurrent Multimodal Data Acquisition During Brain Scanning is within Reach. https://doi.org/10.1101/2021.09.07.459353

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

KEEP EXPLORING

Related preprints

Epidermal Langerhans Cells Act as Neuroimmune Regulators of Pain and Itch

Neuroimmune interactions in the skin coordinate immune defense and somatosensory perception, yet how immune cells shape sensory signaling remains poorly defined. Here, we show that Langerhans cells (LCs), epidermal antigen-presenting cells, function as local immune-derived amplifiers of cutaneous sensory signaling. Anatomical and transcriptomic analyses reveal preferential LC association with non-peptidergic sensory neurons. LC activation increases neuronal and behavioral responses to thermal, mechanical, and pruritic stimuli without directly exciting sensory neurons, whereas LC inhibition or ablation selectively reduces pruritogen-evoked itch. We identified semaphorin 7A as a candidate LC-expressed mediator. Semaphorin 7A sensitized cultured sensory neurons to chloroquine and histamine, and neutralizing semaphorin 7A abolished the increase in chloroquine-evoked scratching produced by LC activation. Its receptor PlexinC1 was expressed by most MrgprA3 pruriceptors and blocking PlexinC1 reduced semaphorin 7A-evoked neuronal responses. Together, these findings identify epidermal LCs as local immune-derived amplifiers that regulate the responsiveness of cutaneous sensory circuits and identify semaphorin 7A as a mediator of LC-induced itch potentiation.

neuroscience↗

Feasible closed-loop stimulation for neural latent dynamics control

Modern neuroscience benefits from powerful computational and experimental methods for studying neural populations, including latent dynamics models that predict behavior with few dimensions. But despite their explanatory utility, latent factors are seldom targeted explicitly with experimental perturbations, leaving causal relationships to behavior and inferred dynamical landscapes untested. A promising solution is closed-loop, multi-channel optogenetic control, which, when paired with model predictions, could steer neural trajectories in real time--a feat impossible for traditional, hand-designed stimulation. However, because closed-loop latent control has not been demonstrated in vivo, the hardware and software requirements remain unclear--particularly the necessary stimulation dimensionality and how limited resources such as implant volume and bandwidth should be allocated between stimulation and recording capabilities. Preliminary experiments would thus help guide ongoing technological development. As large-scale exploration of these design spaces in vivo is prohibitively expensive, we conducted a high-throughput simulation survey using biophysically grounded spiking neural networks. We found that low-dimensional actuation is sufficient: in the reference configuration, ~20% of the stimulation channels achieved ~85% of peak control performance, far fewer than the number of neurons. Furthermore, allocating channels roughly equally between stimulation and recording optimized behavioral control, whereas pairing many electrodes with a single light source--the prevailing practice in experimental labs--performed poorly. Even without heavily optimizing modeling or control, we obtained >60% tracking error reduction and >90% evoked behavior accuracy on average for optimal channel counts. These results held across extensive parameter variations, suggesting that closed-loop latent control is feasible with accessible channel counts and establishing design principles for future tool development and in vivo experiments.

neuroscience↗

Identification of Kinome Biomarkers and Therapeutic Rescue in cGMP-Linked Retinal Degeneration

Inherited retinal degenerations, such as Retinitis Pigmentosa (RP) and Leber's congenital amaurosis (LCA), are major causes of progressive and irreversible vision loss. The large number of genes associated with these disorders makes their clinical and molecular characterization difficult, while systemic biomarkers for disease progression or treatment response remain limited. These challenges were addressed by targeting cGMP-associated mechanisms shared by RP and LCA and integrating systemic biomarker profiling with retinal outcomes. Kinase activity analysis (kinome analysis) in peripheral blood mononuclear cells distinguished healthy and diseased states and captured therapy-associated signatures in rd10 mice treated with LP-CN03, a liposomal formulation of the cGMP analog CN03. This first systemic analysis in a therapeutically responsive animal model highlights kinome analysis as a potential translational readout. Given shared cGMP signaling in RP and AIPL1-associated LCA, LP-CN03's therapeutic potential was further evaluated in a new CRISPR-Cas9-generated Aipl1-/- mouse model. Treatment with LP-CN03 preserved retinal structure and function, as shown by electroretinography, longitudinal optical coherence tomography, fundus imaging, optomotor testing, and photoreceptor-specific gene expression. Together, these findings provide independent in vivo evidence for the neuroprotective effect of LP-CN03 in both cGMP-related RP and LCA, also highlighting the translational value of kinome profiling.

neuroscience↗