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Neuromodulation accompanying focused ultrasound-induced blood-brain barrier opening

Burst-mode focused ultrasound (FUS) induces microbubble cavitation in the vasculature and temporarily disrupts the blood-brain barrier (BBB) to enable therapeutic agent delivery. However, it remains unclear whether FUS-induced BBB opening is accompanied by neuromodulation. Here we characterized the...

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Autores principales: Chu, Po-Chun, Liu, Hao-Li, Lai, Hsin-Yi, Lin, Chung-Yin, Tsai, Hong-Chieh, Pei, Yu-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614673/
https://www.ncbi.nlm.nih.gov/pubmed/26490653
http://dx.doi.org/10.1038/srep15477
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author Chu, Po-Chun
Liu, Hao-Li
Lai, Hsin-Yi
Lin, Chung-Yin
Tsai, Hong-Chieh
Pei, Yu-Cheng
author_facet Chu, Po-Chun
Liu, Hao-Li
Lai, Hsin-Yi
Lin, Chung-Yin
Tsai, Hong-Chieh
Pei, Yu-Cheng
author_sort Chu, Po-Chun
collection PubMed
description Burst-mode focused ultrasound (FUS) induces microbubble cavitation in the vasculature and temporarily disrupts the blood-brain barrier (BBB) to enable therapeutic agent delivery. However, it remains unclear whether FUS-induced BBB opening is accompanied by neuromodulation. Here we characterized the functional effects of FUS-induced BBB opening by measuring changes in somatosensory evoked potentials (SSEPs) and blood-oxygen-level dependent (BOLD) responses. Rats underwent burst-mode FUS (mechanical index (MI) of 0.3, 0.55 or 0.8) to the forelimb region in the left primary somatosensory cortex to induce BBB opening. Longitudinal measurements were followed for up to 1 week to characterize the temporal dynamics of neuromodulation. We observed that 0.8-MI FUS profoundly suppressed SSEP amplitude and prolonged latency, and this effect lasted 7 days. 0.55-MI FUS resulted in minimal and short-term suppression of SSEP for less than 60 minutes and didn’t affect latency. BOLD responses were also suppressed in an MI-dependent manner, mirroring the effect on SSEPs. Furthermore, repetitive delivery of 0.55-MI FUS every 3 days elicited no accumulative effects on SSEPs or tissue integrity. This is the first evidence that FUS-induced BBB opening is accompanied by reversible changes in neuron responses, and may provide valuable insight toward the development of FUS-induced BBB opening for clinical applications.
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spelling pubmed-46146732015-10-29 Neuromodulation accompanying focused ultrasound-induced blood-brain barrier opening Chu, Po-Chun Liu, Hao-Li Lai, Hsin-Yi Lin, Chung-Yin Tsai, Hong-Chieh Pei, Yu-Cheng Sci Rep Article Burst-mode focused ultrasound (FUS) induces microbubble cavitation in the vasculature and temporarily disrupts the blood-brain barrier (BBB) to enable therapeutic agent delivery. However, it remains unclear whether FUS-induced BBB opening is accompanied by neuromodulation. Here we characterized the functional effects of FUS-induced BBB opening by measuring changes in somatosensory evoked potentials (SSEPs) and blood-oxygen-level dependent (BOLD) responses. Rats underwent burst-mode FUS (mechanical index (MI) of 0.3, 0.55 or 0.8) to the forelimb region in the left primary somatosensory cortex to induce BBB opening. Longitudinal measurements were followed for up to 1 week to characterize the temporal dynamics of neuromodulation. We observed that 0.8-MI FUS profoundly suppressed SSEP amplitude and prolonged latency, and this effect lasted 7 days. 0.55-MI FUS resulted in minimal and short-term suppression of SSEP for less than 60 minutes and didn’t affect latency. BOLD responses were also suppressed in an MI-dependent manner, mirroring the effect on SSEPs. Furthermore, repetitive delivery of 0.55-MI FUS every 3 days elicited no accumulative effects on SSEPs or tissue integrity. This is the first evidence that FUS-induced BBB opening is accompanied by reversible changes in neuron responses, and may provide valuable insight toward the development of FUS-induced BBB opening for clinical applications. Nature Publishing Group 2015-10-22 /pmc/articles/PMC4614673/ /pubmed/26490653 http://dx.doi.org/10.1038/srep15477 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Chu, Po-Chun
Liu, Hao-Li
Lai, Hsin-Yi
Lin, Chung-Yin
Tsai, Hong-Chieh
Pei, Yu-Cheng
Neuromodulation accompanying focused ultrasound-induced blood-brain barrier opening
title Neuromodulation accompanying focused ultrasound-induced blood-brain barrier opening
title_full Neuromodulation accompanying focused ultrasound-induced blood-brain barrier opening
title_fullStr Neuromodulation accompanying focused ultrasound-induced blood-brain barrier opening
title_full_unstemmed Neuromodulation accompanying focused ultrasound-induced blood-brain barrier opening
title_short Neuromodulation accompanying focused ultrasound-induced blood-brain barrier opening
title_sort neuromodulation accompanying focused ultrasound-induced blood-brain barrier opening
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614673/
https://www.ncbi.nlm.nih.gov/pubmed/26490653
http://dx.doi.org/10.1038/srep15477
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