Cargando…
Near-Infrared Light Increases Functional Connectivity with a Non-thermal Mechanism
Although techniques for noninvasive brain stimulation are under intense investigation, an approach that has received limited attention is transcranial photobiomodulation (tPBM), the delivery of near-infrared light to the brain with a laser or light-emitting diode directed at the scalp. Here we emplo...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152883/ https://www.ncbi.nlm.nih.gov/pubmed/34296085 http://dx.doi.org/10.1093/texcom/tgaa004 |
_version_ | 1783698685157179392 |
---|---|
author | Dmochowski, Grzegorz M Shereen, Ahmed Duke Berisha, Destiny Dmochowski, Jacek P |
author_facet | Dmochowski, Grzegorz M Shereen, Ahmed Duke Berisha, Destiny Dmochowski, Jacek P |
author_sort | Dmochowski, Grzegorz M |
collection | PubMed |
description | Although techniques for noninvasive brain stimulation are under intense investigation, an approach that has received limited attention is transcranial photobiomodulation (tPBM), the delivery of near-infrared light to the brain with a laser or light-emitting diode directed at the scalp. Here we employed functional magnetic resonance imaging to measure the blood-oxygenation-level–dependent signal in n = 20 healthy human participants while concurrently stimulating their right frontal pole with a near-infrared laser. Functional connectivity with the illuminated region increased by up to 15% during stimulation, with a quarter of all connections experiencing a significant increase. The time course of connectivity exhibited a sharp rise approximately 1 min after illumination onset. Brain-wide connectivity increases were also observed, with connections involving the stimulated hemisphere showing a significantly larger increase than those in the contralateral hemisphere. We subsequently employed magnetic resonance thermometry to measure brain temperature during tPBM (separate cohort, n = 20) and found no significant temperature differences between active and sham stimulation. Our findings suggest that near-infrared light synchronizes brain activity with a nonthermal mechanism, underscoring the promise of tPBM as a new technique for stimulating brain function. |
format | Online Article Text |
id | pubmed-8152883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81528832021-07-21 Near-Infrared Light Increases Functional Connectivity with a Non-thermal Mechanism Dmochowski, Grzegorz M Shereen, Ahmed Duke Berisha, Destiny Dmochowski, Jacek P Cereb Cortex Commun Original Article Although techniques for noninvasive brain stimulation are under intense investigation, an approach that has received limited attention is transcranial photobiomodulation (tPBM), the delivery of near-infrared light to the brain with a laser or light-emitting diode directed at the scalp. Here we employed functional magnetic resonance imaging to measure the blood-oxygenation-level–dependent signal in n = 20 healthy human participants while concurrently stimulating their right frontal pole with a near-infrared laser. Functional connectivity with the illuminated region increased by up to 15% during stimulation, with a quarter of all connections experiencing a significant increase. The time course of connectivity exhibited a sharp rise approximately 1 min after illumination onset. Brain-wide connectivity increases were also observed, with connections involving the stimulated hemisphere showing a significantly larger increase than those in the contralateral hemisphere. We subsequently employed magnetic resonance thermometry to measure brain temperature during tPBM (separate cohort, n = 20) and found no significant temperature differences between active and sham stimulation. Our findings suggest that near-infrared light synchronizes brain activity with a nonthermal mechanism, underscoring the promise of tPBM as a new technique for stimulating brain function. Oxford University Press 2020-03-19 /pmc/articles/PMC8152883/ /pubmed/34296085 http://dx.doi.org/10.1093/texcom/tgaa004 Text en © The Author(s) 2020. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Dmochowski, Grzegorz M Shereen, Ahmed Duke Berisha, Destiny Dmochowski, Jacek P Near-Infrared Light Increases Functional Connectivity with a Non-thermal Mechanism |
title | Near-Infrared Light Increases Functional Connectivity with a Non-thermal Mechanism |
title_full | Near-Infrared Light Increases Functional Connectivity with a Non-thermal Mechanism |
title_fullStr | Near-Infrared Light Increases Functional Connectivity with a Non-thermal Mechanism |
title_full_unstemmed | Near-Infrared Light Increases Functional Connectivity with a Non-thermal Mechanism |
title_short | Near-Infrared Light Increases Functional Connectivity with a Non-thermal Mechanism |
title_sort | near-infrared light increases functional connectivity with a non-thermal mechanism |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152883/ https://www.ncbi.nlm.nih.gov/pubmed/34296085 http://dx.doi.org/10.1093/texcom/tgaa004 |
work_keys_str_mv | AT dmochowskigrzegorzm nearinfraredlightincreasesfunctionalconnectivitywithanonthermalmechanism AT shereenahmedduke nearinfraredlightincreasesfunctionalconnectivitywithanonthermalmechanism AT berishadestiny nearinfraredlightincreasesfunctionalconnectivitywithanonthermalmechanism AT dmochowskijacekp nearinfraredlightincreasesfunctionalconnectivitywithanonthermalmechanism |