Upconversion‐Based Remote Deep Brain Modulation for Therapeutic Dissection of Parkinson's Disease

Abstract High frequency deep brain stimulation (DBS) is widely used for improving motor capability in patients with Parkinson's disease (PD). Here, an upconversion‐based strategy is described for remote deep brain modulation, which is an all‐optical solution for treating PD in rodent animals without any tethering interferences. It is demonstrated that both high frequency stimulation and inhibition of subthalamic nucleus (STN), can improve the motor function of Hemi‐Parkinsonian rodent models, potentially providing a specific and flexible therapeutic alternative for treating PD. A multi‐modal approach is further taken that combines optogenetics and electrophysiology recording, and found that high frequency optogenetic inhibition of STN work similarly as high frequency activation to rescue the pathologic electrical activity in the motor cortex and restore the motor deficiency in Hemi‐Parkinsonian rodents. It is also shown that indirect inhibitory modification of entopeduncular nucleus (EP) within the basal ganglia system, which is induced by either STN inhibition or activation, plays a critical role in the STN‐DBS induced therapeutic effects in the Hemi‐Parkinsonian animals. These results provide first experimental evidence supporting a working principle of STN‐DBS by disruption of anterograde signal transmission along the indirect pathway of basal ganglia, and can be instructive for future clinical treatment of PD with DBS.

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Publication Details

Journal
Advanced Therapeutics
Published
2025-04-14
DOI
https://doi.org/10.1002/adtp.202400543
Citations
1
Primary Topic
Neurological disorders and treatments
Type
article
Field-Weighted Citation Impact
1.39

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Upconversion‐Based Remote Deep Brain Modulation for Therapeutic Dissection of Parkinson's Disease

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Advanced Therapeutics
Neurological disorders and treatments
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article

Upconversion‐Based Remote Deep Brain Modulation for Therapeutic Dissection of Parkinson's Disease

Kai Xie, Xudong Lin, Jufang He, Haibing Yue, Zixun Wang, Wing‐Ho Yung, Wenchong Zhang, Peng Shi, Feng Wang, Tianying Sun, Xi Chen, Ming Liu, Zhen Xu, Qinghai Liao
article en
1 citations

Abstract

Abstract High frequency deep brain stimulation (DBS) is widely used for improving motor capability in patients with Parkinson's disease (PD). Here, an upconversion‐based strategy is described for remote deep brain modulation, which is an all‐optical solution for treating PD in rodent animals without any tethering interferences. It is demonstrated that both high frequency stimulation and inhibition of subthalamic nucleus (STN), can improve the motor function of Hemi‐Parkinsonian rodent models, potentially providing a specific and flexible therapeutic alternative for treating PD. A multi‐modal approach is further taken that combines optogenetics and electrophysiology recording, and found that high frequency optogenetic inhibition of STN work similarly as high frequency activation to rescue the pathologic electrical activity in the motor cortex and restore the motor deficiency in Hemi‐Parkinsonian rodents. It is also shown that indirect inhibitory modification of entopeduncular nucleus (EP) within the basal ganglia system, which is induced by either STN inhibition or activation, plays a critical role in the STN‐DBS induced therapeutic effects in the Hemi‐Parkinsonian animals. These results provide first experimental evidence supporting a working principle of STN‐DBS by disruption of anterograde signal transmission along the indirect pathway of basal ganglia, and can be instructive for future clinical treatment of PD with DBS.

Advanced TherapeuticsVol. 8(6)
Sun Yat-sen University (CN), City University of Hong Kong (HK), Hong Kong University of Science and Technology (HK), City University of Hong Kong, Shenzhen Research Institute (CN), University of Hong Kong (HK)
City University of Hong Kong, National Natural Science Foundation of China, Innovation and Technology Commission
Openalex Percentile: Top 21%
Neurological disorders and treatments
1.39
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