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High resolution ultrasonic neural modulation observed via in vivo two-photon calcium imaging
Neural modulation plays a major role in delineating the circuit mechanisms and serves as the cornerstone of neural interface technologies. Among the various modulation mechanisms, ultrasound enables noninvasive label-free deep access to mammalian brain tissue. To date, most if not all ultrasonic neu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169577/ https://www.ncbi.nlm.nih.gov/pubmed/34952226 http://dx.doi.org/10.1016/j.brs.2021.12.005 |
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author | Cheng, Zongyue Wang, Chenmao Wei, Bowen Gan, Wenbiao Zhou, Qifa Cui, Meng |
author_facet | Cheng, Zongyue Wang, Chenmao Wei, Bowen Gan, Wenbiao Zhou, Qifa Cui, Meng |
author_sort | Cheng, Zongyue |
collection | PubMed |
description | Neural modulation plays a major role in delineating the circuit mechanisms and serves as the cornerstone of neural interface technologies. Among the various modulation mechanisms, ultrasound enables noninvasive label-free deep access to mammalian brain tissue. To date, most if not all ultrasonic neural modulation implementations are based on ~1 MHz carrier frequency. The long acoustic wavelength results in a spatially coarse modulation zone, often spanning over multiple function regions. The modulation of one function region is inevitably linked with the modulation of its neighboring regions. Moreover, the lack of in vivo cellular resolution cell-type-specific recording capabilities in most studies prevents the revealing of the genuine cellular response to ultrasound. To significantly increase the spatial resolution, we explored the application of high-frequency ultrasound. To investigate the neuronal response at cellular resolutions, we developed a dual-modality system combining in vivo two-photon calcium imaging and focused ultrasound modulation. The studies show that the ~30 MHz ultrasound can suppress the neuronal activity in awake mice at 100-mm scale spatial resolutions, paving the way for high-resolution ultrasonic neural modulation. The dual-modality in vivo system validated through this study will serve as a general platform for studying the dynamics of various cell types in response to ultrasound. |
format | Online Article Text |
id | pubmed-9169577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-91695772022-06-06 High resolution ultrasonic neural modulation observed via in vivo two-photon calcium imaging Cheng, Zongyue Wang, Chenmao Wei, Bowen Gan, Wenbiao Zhou, Qifa Cui, Meng Brain Stimul Article Neural modulation plays a major role in delineating the circuit mechanisms and serves as the cornerstone of neural interface technologies. Among the various modulation mechanisms, ultrasound enables noninvasive label-free deep access to mammalian brain tissue. To date, most if not all ultrasonic neural modulation implementations are based on ~1 MHz carrier frequency. The long acoustic wavelength results in a spatially coarse modulation zone, often spanning over multiple function regions. The modulation of one function region is inevitably linked with the modulation of its neighboring regions. Moreover, the lack of in vivo cellular resolution cell-type-specific recording capabilities in most studies prevents the revealing of the genuine cellular response to ultrasound. To significantly increase the spatial resolution, we explored the application of high-frequency ultrasound. To investigate the neuronal response at cellular resolutions, we developed a dual-modality system combining in vivo two-photon calcium imaging and focused ultrasound modulation. The studies show that the ~30 MHz ultrasound can suppress the neuronal activity in awake mice at 100-mm scale spatial resolutions, paving the way for high-resolution ultrasonic neural modulation. The dual-modality in vivo system validated through this study will serve as a general platform for studying the dynamics of various cell types in response to ultrasound. 2022 2021-12-21 /pmc/articles/PMC9169577/ /pubmed/34952226 http://dx.doi.org/10.1016/j.brs.2021.12.005 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Cheng, Zongyue Wang, Chenmao Wei, Bowen Gan, Wenbiao Zhou, Qifa Cui, Meng High resolution ultrasonic neural modulation observed via in vivo two-photon calcium imaging |
title | High resolution ultrasonic neural modulation observed via in vivo two-photon calcium imaging |
title_full | High resolution ultrasonic neural modulation observed via in vivo two-photon calcium imaging |
title_fullStr | High resolution ultrasonic neural modulation observed via in vivo two-photon calcium imaging |
title_full_unstemmed | High resolution ultrasonic neural modulation observed via in vivo two-photon calcium imaging |
title_short | High resolution ultrasonic neural modulation observed via in vivo two-photon calcium imaging |
title_sort | high resolution ultrasonic neural modulation observed via in vivo two-photon calcium imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169577/ https://www.ncbi.nlm.nih.gov/pubmed/34952226 http://dx.doi.org/10.1016/j.brs.2021.12.005 |
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