Cargando…

Non-invasive ultrasonic neuromodulation of neuronal excitability for treatment of epilepsy

Non-invasive low-intensity pulsed ultrasound has been employed for direct neuro-modulation. However, its range and effectiveness for different neurological disorders have not been fully elucidated. Methods: We used multiple approaches of electrophysiology, immunohistochemistry, and behavioral tests...

Descripción completa

Detalles Bibliográficos
Autores principales: Lin, Zhengrong, Meng, Long, Zou, Junjie, Zhou, Wei, Huang, Xiaowei, Xue, Shan, Bian, Tianyuan, Yuan, Tifei, Niu, Lili, Guo, Yanwu, Zheng, Hairong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196311/
https://www.ncbi.nlm.nih.gov/pubmed/32373225
http://dx.doi.org/10.7150/thno.40520
_version_ 1783528700452536320
author Lin, Zhengrong
Meng, Long
Zou, Junjie
Zhou, Wei
Huang, Xiaowei
Xue, Shan
Bian, Tianyuan
Yuan, Tifei
Niu, Lili
Guo, Yanwu
Zheng, Hairong
author_facet Lin, Zhengrong
Meng, Long
Zou, Junjie
Zhou, Wei
Huang, Xiaowei
Xue, Shan
Bian, Tianyuan
Yuan, Tifei
Niu, Lili
Guo, Yanwu
Zheng, Hairong
author_sort Lin, Zhengrong
collection PubMed
description Non-invasive low-intensity pulsed ultrasound has been employed for direct neuro-modulation. However, its range and effectiveness for different neurological disorders have not been fully elucidated. Methods: We used multiple approaches of electrophysiology, immunohistochemistry, and behavioral tests as potential epilepsy treatments in non-human primate model of epilepsy and human epileptic tissues. Low-intensity pulsed ultrasound with a frequency of 750 kHz and acoustic pressure of 0.35 MPa (the spatial peak pulse average intensity, I(SPPA) = 2.02 W/cm(2)) were delivered to the epileptogenic foci in five penicillin-induced epileptic monkey models. An ultrasound neuro-modulation system with a frequency of 28 MHz and acoustic pressure of 0.13 MPa (I(SPPA) = 465 mW/cm(2)) compatible with patch-clamp systems was used to stimulate the brain slices prepared from fifteen patients with epilepsy. Results: After 30 min of low-intensity pulsed ultrasound treatment, total seizure count for 16 hours (sham group: 107.7 ± 1.2, ultrasound group: 66.0 ± 7.9, P < 0.01) and seizure frequency per hour (sham group: 15.6 ± 1.2, ultrasound group: 9.6 ± 1.5, P < 0.05) were significantly reduced. The therapeutic efficacy and underlying potential mechanism of low-intensity pulsed ultrasound treatment were studied in biopsy specimens from epileptic patients in vitro. Ultrasound stimulation could inhibit epileptiform activities with an efficiency exceeding 65%, potentially due to adjusting the balance of excitatory-inhibitory (E/I) synaptic inputs by the increased activity of local inhibitory neurons. Conclusion: Herein, we demonstrated for the first time that low-intensity pulsed ultrasound improves electrophysiological activities and behavioral outcomes in a non-human primate model of epilepsy and suppresses epileptiform activities of neurons from human epileptic slices. The study provides evidence for the potential clinical use of non-invasive low-intensity pulsed ultrasound stimulation for epilepsy treatment.
format Online
Article
Text
id pubmed-7196311
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-71963112020-05-05 Non-invasive ultrasonic neuromodulation of neuronal excitability for treatment of epilepsy Lin, Zhengrong Meng, Long Zou, Junjie Zhou, Wei Huang, Xiaowei Xue, Shan Bian, Tianyuan Yuan, Tifei Niu, Lili Guo, Yanwu Zheng, Hairong Theranostics Research Paper Non-invasive low-intensity pulsed ultrasound has been employed for direct neuro-modulation. However, its range and effectiveness for different neurological disorders have not been fully elucidated. Methods: We used multiple approaches of electrophysiology, immunohistochemistry, and behavioral tests as potential epilepsy treatments in non-human primate model of epilepsy and human epileptic tissues. Low-intensity pulsed ultrasound with a frequency of 750 kHz and acoustic pressure of 0.35 MPa (the spatial peak pulse average intensity, I(SPPA) = 2.02 W/cm(2)) were delivered to the epileptogenic foci in five penicillin-induced epileptic monkey models. An ultrasound neuro-modulation system with a frequency of 28 MHz and acoustic pressure of 0.13 MPa (I(SPPA) = 465 mW/cm(2)) compatible with patch-clamp systems was used to stimulate the brain slices prepared from fifteen patients with epilepsy. Results: After 30 min of low-intensity pulsed ultrasound treatment, total seizure count for 16 hours (sham group: 107.7 ± 1.2, ultrasound group: 66.0 ± 7.9, P < 0.01) and seizure frequency per hour (sham group: 15.6 ± 1.2, ultrasound group: 9.6 ± 1.5, P < 0.05) were significantly reduced. The therapeutic efficacy and underlying potential mechanism of low-intensity pulsed ultrasound treatment were studied in biopsy specimens from epileptic patients in vitro. Ultrasound stimulation could inhibit epileptiform activities with an efficiency exceeding 65%, potentially due to adjusting the balance of excitatory-inhibitory (E/I) synaptic inputs by the increased activity of local inhibitory neurons. Conclusion: Herein, we demonstrated for the first time that low-intensity pulsed ultrasound improves electrophysiological activities and behavioral outcomes in a non-human primate model of epilepsy and suppresses epileptiform activities of neurons from human epileptic slices. The study provides evidence for the potential clinical use of non-invasive low-intensity pulsed ultrasound stimulation for epilepsy treatment. Ivyspring International Publisher 2020-04-12 /pmc/articles/PMC7196311/ /pubmed/32373225 http://dx.doi.org/10.7150/thno.40520 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Lin, Zhengrong
Meng, Long
Zou, Junjie
Zhou, Wei
Huang, Xiaowei
Xue, Shan
Bian, Tianyuan
Yuan, Tifei
Niu, Lili
Guo, Yanwu
Zheng, Hairong
Non-invasive ultrasonic neuromodulation of neuronal excitability for treatment of epilepsy
title Non-invasive ultrasonic neuromodulation of neuronal excitability for treatment of epilepsy
title_full Non-invasive ultrasonic neuromodulation of neuronal excitability for treatment of epilepsy
title_fullStr Non-invasive ultrasonic neuromodulation of neuronal excitability for treatment of epilepsy
title_full_unstemmed Non-invasive ultrasonic neuromodulation of neuronal excitability for treatment of epilepsy
title_short Non-invasive ultrasonic neuromodulation of neuronal excitability for treatment of epilepsy
title_sort non-invasive ultrasonic neuromodulation of neuronal excitability for treatment of epilepsy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196311/
https://www.ncbi.nlm.nih.gov/pubmed/32373225
http://dx.doi.org/10.7150/thno.40520
work_keys_str_mv AT linzhengrong noninvasiveultrasonicneuromodulationofneuronalexcitabilityfortreatmentofepilepsy
AT menglong noninvasiveultrasonicneuromodulationofneuronalexcitabilityfortreatmentofepilepsy
AT zoujunjie noninvasiveultrasonicneuromodulationofneuronalexcitabilityfortreatmentofepilepsy
AT zhouwei noninvasiveultrasonicneuromodulationofneuronalexcitabilityfortreatmentofepilepsy
AT huangxiaowei noninvasiveultrasonicneuromodulationofneuronalexcitabilityfortreatmentofepilepsy
AT xueshan noninvasiveultrasonicneuromodulationofneuronalexcitabilityfortreatmentofepilepsy
AT biantianyuan noninvasiveultrasonicneuromodulationofneuronalexcitabilityfortreatmentofepilepsy
AT yuantifei noninvasiveultrasonicneuromodulationofneuronalexcitabilityfortreatmentofepilepsy
AT niulili noninvasiveultrasonicneuromodulationofneuronalexcitabilityfortreatmentofepilepsy
AT guoyanwu noninvasiveultrasonicneuromodulationofneuronalexcitabilityfortreatmentofepilepsy
AT zhenghairong noninvasiveultrasonicneuromodulationofneuronalexcitabilityfortreatmentofepilepsy