Holographic Ultrasound Modulates Neural Activity in a 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine-Induced Mouse Model of Parkinson's Disease.

IF 11 1区 综合性期刊 Q1 Multidisciplinary
Research Pub Date : 2024-11-06 eCollection Date: 2024-01-01 DOI:10.34133/research.0516
Hui Zhou, Fei Li, Zhengrong Lin, Long Meng, Dan Chen, Qingping Zhang, Lili Niu
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引用次数: 0

Abstract

Ultrasound (US) has emerged as a noninvasive neurostimulation method for motor control in Parkinson's disease (PD). Previous in vivo US neuromodulation studies for PD were single-target stimulation. However, the motor symptoms of PD are linked with neural circuit dysfunction, and multi-target stimulation is conducted in clinical treatment for PD. Thus, in the present study, we achieved multi-target US stimulation using holographic lens transducer based on the Rayleigh-Sommerfeld diffraction integral and time-reversal methods. We demonstrated that holographic US stimulation of the bilateral dorsal striatum (DS) could improve the motor function in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced mouse model of PD. The holographic US wave (fundamental frequency: 3 MHz, pulse repetition frequency: 500 Hz, duty cycle: 20%, tone-burst duration: 0.4 ms, sonication duration: 1 s, interstimulus interval: 4 s, spatial-peak temporal-average intensity: 180 mw/cm2) was delivered to the bilateral DS 20 min per day for consecutive 10 d after the last injection of MPTP. Immunohistochemical c-Fos staining demonstrated that holographic US significantly increased the c-Fos-positive neurons in the bilateral DS compared with the sham group (P = 0.003). Moreover, our results suggested that holographic US stimulation of the bilateral DS ameliorated motor dysfunction (P < 0.05) and protected the dopaminergic (DA) neurons (P < 0.001). The neuroprotective effect of holographic US was associated with the prevention of axon degeneration and the reinforcement of postsynaptic densities [growth associated protein-43 (P < 0.001), phosphorylated Akt (P = 0.001), β3-tubulin (P < 0.001), phosphorylated CRMP2 (P = 0.037), postsynaptic density (P = 0.023)]. These data suggested that holographic US-induced acoustic radiation force has the potential to achieve multi-target neuromodulation and could serve as a reliable tool for the treatment of PD.

全息超声调节 1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的帕金森病小鼠模型的神经活动。
超声波(US)已成为一种非侵入性神经刺激方法,用于帕金森病(PD)的运动控制。之前针对帕金森病的体内 US 神经调控研究都是单目标刺激。然而,帕金森病的运动症状与神经回路功能障碍有关,因此临床治疗帕金森病时采用了多靶点刺激。因此,在本研究中,我们基于瑞利-索默费尔德衍射积分法和时间反转法,利用全息透镜换能器实现了多靶点US刺激。我们证实了全息 US 刺激双侧背侧纹状体(DS)可以改善 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的帕金森病小鼠模型的运动功能。全息 US 波(基频:3 MHz,脉冲重复频率:500 Hz,占空比:20%,音爆持续时间:0.4 ms,超声持续时间:0.5 ms)可改善 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的帕金森病小鼠的运动功能:0.4毫秒,超声持续时间1秒,刺激间隔在最后一次注射 MPTP 后的连续 10 天内,每天对双侧 DS 连续注射 20 分钟(4 秒,空间-峰值-时间-平均强度:180 mw/cm2)。免疫组化 c-Fos 染色表明,与假组相比,全息 US 能显著增加双侧 DS 中 c-Fos 阳性神经元的数量(P = 0.003)。此外,我们的结果表明,全息 US 刺激双侧 DS 可改善运动功能障碍(P < 0.05)并保护多巴胺能(DA)神经元(P < 0.001)。全息 US 的神经保护作用与轴突变性的预防和突触后密度的加强有关 [生长相关蛋白-43(P < 0.001)、磷酸化 Akt(P = 0.001)、β3-tubulin(P < 0.001)、磷酸化 CRMP2(P = 0.037)、突触后密度(P = 0.023)]。这些数据表明,全息美国诱导声辐射力具有实现多靶点神经调节的潜力,可作为治疗帕金森病的可靠工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Research
Research Multidisciplinary-Multidisciplinary
CiteScore
13.40
自引率
3.60%
发文量
0
审稿时长
14 weeks
期刊介绍: Research serves as a global platform for academic exchange, collaboration, and technological advancements. This journal welcomes high-quality research contributions from any domain, with open arms to authors from around the globe. Comprising fundamental research in the life and physical sciences, Research also highlights significant findings and issues in engineering and applied science. The journal proudly features original research articles, reviews, perspectives, and editorials, fostering a diverse and dynamic scholarly environment.
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