Focal thalamic infrared neural stimulation propagates dynamical transformations in auditory cortex

<i>Objective.</i>Infrared neural stimulation (INS) has emerged as a potent neuromodulation technology, offering safe and focal stimulation with superior spatial recruitment profiles compared to conventional electrical methods. However, the neural dynamics induced by INS stimulation remain poorly understood. Elucidating these dynamics will help develop new INS stimulation paradigms and advance its clinical application.<i>Approach.</i>In this study, we assessed the local network dynamics of INS entrainment in the auditory thalamocortical circuit using the chronically implanted rat model. Our approach focused on measuring INS energy-based local field potential (LFP) recruitment induced by focal thalamocortical stimulation. We further characterized linear and nonlinear oscillatory LFP activity in response to single-pulse and periodic INS and performed spectral decomposition to uncover specific LFP band entrainment to INS. Finally, we examined spike-field transformations across the thalamocortical synapse using spike-LFP coherence coupling measures.<i>Main results.</i>We found that INS significantly increases LFP amplitude as a log-linear function of INS energy per pulse, primarily entraining to LFP<i>β</i>and<i>γ</i>bands with synchrony extending to 200 Hz in some cases. A subset of neurons demonstrated nonlinear, chaotic oscillations linked to information transfer across cortical circuits. Finally, we utilized spike-field coherences to correlate spike coupling to LFP frequency band activity and suggest an energy-dependent model of network activation resulting from INS stimulation.<i>Significance.</i>We show that INS reliably drives robust network activity and can potently modulate cortical field potentials across a wide range of frequencies in a stimulus parameter-dependent manner. Based on these results, we propose design principles for developing full coverage, all-optical thalamocortical auditory neuroprostheses.

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Publication Details

Journal
Journal of Neural Engineering
Published
2025-11-05
DOI
https://doi.org/10.1088/1741-2552/ae1bdb
Citations
1
Primary Topic
Photoreceptor and optogenetics research
Type
article
Field-Weighted Citation Impact
0.91
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article

Focal thalamic infrared neural stimulation propagates dynamical transformations in auditory cortex

Brandon S. Coventry, Cuong P. Luu, Edward L. Bartlett
1 citations
Journal of Neural Engineering
Photoreceptor and optogenetics research
0.91
article

Focal thalamic infrared neural stimulation propagates dynamical transformations in auditory cortex

Brandon S. Coventry, Cuong P. Luu, Edward L. Bartlett
article en
1 citations

Abstract

<i>Objective.</i>Infrared neural stimulation (INS) has emerged as a potent neuromodulation technology, offering safe and focal stimulation with superior spatial recruitment profiles compared to conventional electrical methods. However, the neural dynamics induced by INS stimulation remain poorly understood. Elucidating these dynamics will help develop new INS stimulation paradigms and advance its clinical application.<i>Approach.</i>In this study, we assessed the local network dynamics of INS entrainment in the auditory thalamocortical circuit using the chronically implanted rat model. Our approach focused on measuring INS energy-based local field potential (LFP) recruitment induced by focal thalamocortical stimulation. We further characterized linear and nonlinear oscillatory LFP activity in response to single-pulse and periodic INS and performed spectral decomposition to uncover specific LFP band entrainment to INS. Finally, we examined spike-field transformations across the thalamocortical synapse using spike-LFP coherence coupling measures.<i>Main results.</i>We found that INS significantly increases LFP amplitude as a log-linear function of INS energy per pulse, primarily entraining to LFP<i>β</i>and<i>γ</i>bands with synchrony extending to 200 Hz in some cases. A subset of neurons demonstrated nonlinear, chaotic oscillations linked to information transfer across cortical circuits. Finally, we utilized spike-field coherences to correlate spike coupling to LFP frequency band activity and suggest an energy-dependent model of network activation resulting from INS stimulation.<i>Significance.</i>We show that INS reliably drives robust network activity and can potently modulate cortical field potentials across a wide range of frequencies in a stimulus parameter-dependent manner. Based on these results, we propose design principles for developing full coverage, all-optical thalamocortical auditory neuroprostheses.

Journal of Neural EngineeringVol. 22(6)
University of Wisconsin–Madison (US), Purdue University West Lafayette (US)
Openalex Percentile: Top 20%
Photoreceptor and optogenetics research
0.91
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