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Transient ultrasound stimulation has lasting effects on neuronal excitability

BACKGROUND: Transcranial ultrasound stimulation can acutely modulate brain activity, but the lasting effects on neurons are unknown. OBJECTIVE: To assess the excitability profile of neurons in the hours following transient ultrasound stimulation. METHODS: Primary rat cortical neurons were stimulated...

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Autores principales: Clennell, Benjamin, Steward, Tom G.J., Elley, Meg, Shin, Eunju, Weston, Miles, Drinkwater, Bruce W., Whitcomb, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973721/
https://www.ncbi.nlm.nih.gov/pubmed/33444809
http://dx.doi.org/10.1016/j.brs.2021.01.003
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author Clennell, Benjamin
Steward, Tom G.J.
Elley, Meg
Shin, Eunju
Weston, Miles
Drinkwater, Bruce W.
Whitcomb, Daniel J.
author_facet Clennell, Benjamin
Steward, Tom G.J.
Elley, Meg
Shin, Eunju
Weston, Miles
Drinkwater, Bruce W.
Whitcomb, Daniel J.
author_sort Clennell, Benjamin
collection PubMed
description BACKGROUND: Transcranial ultrasound stimulation can acutely modulate brain activity, but the lasting effects on neurons are unknown. OBJECTIVE: To assess the excitability profile of neurons in the hours following transient ultrasound stimulation. METHODS: Primary rat cortical neurons were stimulated with a 40 s, 200 kHz pulsed ultrasound stimulation or sham-stimulation. Intrinsic firing properties were investigated through whole-cell patch-clamp recording by evoking action potentials in response to somatic current injection. Recordings were taken at set timepoints following ultrasound stimulation: 0–2 h, 6–8 h, 12–14 h and 24–26 h. Transmission electron microscopy was used to assess synaptic ultrastructure at the same timepoints. RESULTS: In the 0–2 h window, neurons stimulated with ultrasound displayed an increase in the mean frequency of evoked action potentials of 32% above control cell levels (p = 0.023). After 4–6 h this increase was measured as 44% (p = 0.0043). By 12–14 h this effect was eliminated and remained absent 24–26 h post-stimulation. These changes to action potential firing occurred in conjunction with statistically significant differences between control and ultrasound-stimulated neurons in action potential half-width, depolarisation rate, and repolarisation rate, that were similarly eliminated by 24 h following stimulation. These effects occurred in the absence of alterations to intrinsic membrane properties or synaptic ultrastructure. CONCLUSION: We report that stimulating neurons with 40 s of ultrasound enhances their excitability for up to 8 h in conjunction with modifications to action potential kinetics. This occurs in the absence of major ultrastructural change or modification of intrinsic membrane properties. These results can inform the application of transcranial ultrasound in experimental and therapeutic settings.
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spelling pubmed-79737212021-03-23 Transient ultrasound stimulation has lasting effects on neuronal excitability Clennell, Benjamin Steward, Tom G.J. Elley, Meg Shin, Eunju Weston, Miles Drinkwater, Bruce W. Whitcomb, Daniel J. Brain Stimul Article BACKGROUND: Transcranial ultrasound stimulation can acutely modulate brain activity, but the lasting effects on neurons are unknown. OBJECTIVE: To assess the excitability profile of neurons in the hours following transient ultrasound stimulation. METHODS: Primary rat cortical neurons were stimulated with a 40 s, 200 kHz pulsed ultrasound stimulation or sham-stimulation. Intrinsic firing properties were investigated through whole-cell patch-clamp recording by evoking action potentials in response to somatic current injection. Recordings were taken at set timepoints following ultrasound stimulation: 0–2 h, 6–8 h, 12–14 h and 24–26 h. Transmission electron microscopy was used to assess synaptic ultrastructure at the same timepoints. RESULTS: In the 0–2 h window, neurons stimulated with ultrasound displayed an increase in the mean frequency of evoked action potentials of 32% above control cell levels (p = 0.023). After 4–6 h this increase was measured as 44% (p = 0.0043). By 12–14 h this effect was eliminated and remained absent 24–26 h post-stimulation. These changes to action potential firing occurred in conjunction with statistically significant differences between control and ultrasound-stimulated neurons in action potential half-width, depolarisation rate, and repolarisation rate, that were similarly eliminated by 24 h following stimulation. These effects occurred in the absence of alterations to intrinsic membrane properties or synaptic ultrastructure. CONCLUSION: We report that stimulating neurons with 40 s of ultrasound enhances their excitability for up to 8 h in conjunction with modifications to action potential kinetics. This occurs in the absence of major ultrastructural change or modification of intrinsic membrane properties. These results can inform the application of transcranial ultrasound in experimental and therapeutic settings. Elsevier 2021 /pmc/articles/PMC7973721/ /pubmed/33444809 http://dx.doi.org/10.1016/j.brs.2021.01.003 Text en © 2021 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Clennell, Benjamin
Steward, Tom G.J.
Elley, Meg
Shin, Eunju
Weston, Miles
Drinkwater, Bruce W.
Whitcomb, Daniel J.
Transient ultrasound stimulation has lasting effects on neuronal excitability
title Transient ultrasound stimulation has lasting effects on neuronal excitability
title_full Transient ultrasound stimulation has lasting effects on neuronal excitability
title_fullStr Transient ultrasound stimulation has lasting effects on neuronal excitability
title_full_unstemmed Transient ultrasound stimulation has lasting effects on neuronal excitability
title_short Transient ultrasound stimulation has lasting effects on neuronal excitability
title_sort transient ultrasound stimulation has lasting effects on neuronal excitability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973721/
https://www.ncbi.nlm.nih.gov/pubmed/33444809
http://dx.doi.org/10.1016/j.brs.2021.01.003
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