BiomaterialsBioengineeringPeer-reviewed journal article
Chronic alteration of Ca2+ and hemodynamic signals induced by intracortical microstimulation in the visual cortex of awake mice
Naofumi SuematsuiD, Alberto L. VazqueziD, Takashi D.Y. KozaiiD
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Abstract
Understanding the chronic effects of intracortical microstimulation (ICMS) and device implantation on cortical function is essential for the development of stable neuroprosthetics. We chronically implanted microelectrode into Thy1-GCaMP6s mice and conducted longitudinal mesoscopic widefield and two-photon Ca2#x002B; imaging alongside intrinsic optical signal recordings over 12 weeks. Six ICMS frequencies (10-500 Hz) and contralateral visual LED stimuli were delivered in repeated sessions. Oxygen extraction fraction (OEF) was estimated from dual-wavelength reflectance, and hemodynamic response functions (HRF) were derived via regularized deconvolution. Over the chronic period, 25-Hz ICMS evoked progressively larger Ca2+ responses whose duration was extending, while spatial spread remained stable around 500 {micro}m. Concurrently, OEF reductions deepened, reflecting increased relative blood supply, and the spatial extent of OEF signals contracted in the first week before expanding by day 21. After discharge-like Ca2+ events emerged in nearly half of mice, predominantly under 25-Hz ICMS. HRF peak amplitude increased between day 0 and days 7-21, with latency decreasing. Chronic ICMS induces progressive potentiation of neuronal and vascular responses alongside local neurovascular uncoupling on day 0 and sustained silencing of spontaneous activity near the implant. These dynamics exhibiting a stabilization 6-7 weeks after the implantation, coupled with frequency-dependent after discharges, underscore the need for adaptive stimulation strategies prior to the stabilization and to prevent the after discharge and implant designs that mitigate local suppression and ensure long-term stability of cortical neuroprostheses.
- organism: mouse
- assay: imaging
- research focus: cell type annotation
- approach: microscopy & imaging analysis
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