神经退行性变
多巴胺能
黑质
脑深部刺激
神经科学
帕金森病
刺激
神经调节
医学
原发性震颤
疾病
生物
内科学
多巴胺
作者
Ching‐Hsiang Fan,Kuo‐Chen Wei,Nai-Hua Chiu,En‐Chi Liao,Hsien‐Chu Wang,Ruo‐Yu Wu,Yi-Ju Ho,Hong‐Lin Chan,Tsung‐Shing Andrew Wang,Ying‐Zu Huang,Tsung‐Hsun Hsieh,Chin‐Hsien Lin,Yu‐Chun Lin,Chih‐Kuang Yeh
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-07-15
卷期号:21 (14): 5967-5976
被引量:29
标识
DOI:10.1021/acs.nanolett.1c00886
摘要
Sonogenetics is a promising strategy allowing the noninvasive and selective activation of targeted neurons in deep brain regions; nevertheless, its therapeutic outcome for neurodegeneration diseases that need long-term treatment remains to be verified. We previously enhanced the ultrasound (US) sensitivity of targeted cells by genetic modification with an engineered auditory-sensing protein, mPrestin (N7T, N308S). In this study, we expressed mPrestin in the dopaminergic neurons of the substantia nigra in Parkinson's disease (PD) mice and used 0.5 MHz US for repeated and localized brain stimulation. The mPrestin expression in dopaminergic neurons persisted for at least 56 days after a single shot of adeno-associated virus, suggesting that the period of expression was long enough for US treatment in mice. Compared to untreated mice, US stimulation ameliorated the dopaminergic neurodegeneration 10-fold and mitigated the PD symptoms of the mice 4-fold, suggesting that this sonogenetic strategy has the clinical potential to treat neurodegenerative diseases.
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