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Abstract
Aims: The open-loop nature of conventional deep brain stimulation (DBS) produces continuous and excessive stimulation to patients which contributes largely to increased prevalence of adverse side effects. Cerebellar ataxia is characterized by abnormal Purkinje cells (PCs) dendritic arborization, loss of PCs and motor coordination, and muscle weakness with no effective treatment. We aim to develop a real-time field-programmable gate array (FPGA) prototype targeting the deep cerebellar nuclei (DCN) to close the loop for ataxia using conditional double knockout mice with deletion of PC-specific LIM homeobox (Lhx)1 and Lhx5, resulting in abnormal dendritic arborization and motor deficits.
Methods: We implanted multielectrode array in the DCN and muscles of ataxia mice. The beneficial effect of open-loop DCN-DBS or closed-loop DCN-DBS was compared by motor behavioral assessments, electromyography (EMG), and neural activities (neurospike and electroencephalogram) in freely moving mice. FPGA board, which performed complex real-time computation, was used for closed-loop DCN-DBS system.
Results: Closed-loop DCN-DBS was triggered only when symptomatic muscle EMG was detected in a real-time manner, which restored motor activities, electroencephalogram activities and neurospike properties completely in ataxia mice. Closed-loop DCN-DBS was more effective than an open-loop paradigm as it reduced the frequency of DBS.
Conclusion: Our real-time FPGA-based DCN-DBS system could be a potential clinical strategy for alleviating cerebellar ataxia and other movement disorders.
© 2024 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd.
Methods: We implanted multielectrode array in the DCN and muscles of ataxia mice. The beneficial effect of open-loop DCN-DBS or closed-loop DCN-DBS was compared by motor behavioral assessments, electromyography (EMG), and neural activities (neurospike and electroencephalogram) in freely moving mice. FPGA board, which performed complex real-time computation, was used for closed-loop DCN-DBS system.
Results: Closed-loop DCN-DBS was triggered only when symptomatic muscle EMG was detected in a real-time manner, which restored motor activities, electroencephalogram activities and neurospike properties completely in ataxia mice. Closed-loop DCN-DBS was more effective than an open-loop paradigm as it reduced the frequency of DBS.
Conclusion: Our real-time FPGA-based DCN-DBS system could be a potential clinical strategy for alleviating cerebellar ataxia and other movement disorders.
© 2024 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd.
| Original language | English |
|---|---|
| Article number | e14638 |
| Journal | CNS Neuroscience and Therapeutics |
| Volume | 30 |
| Issue number | 3 |
| Online published | 15 Mar 2024 |
| DOIs | |
| Publication status | Published - Mar 2024 |
Funding
This work is supported by the Innovation and Technology Commission of the Hong Kong Special Administrative Region Government (ITS/151/17 and ITS/168/19FP) award to Chi Ma.
Research Keywords
- cerebellar ataxia
- cerebellum
- deep brain stimulation
- electroencephalography
- electromyography
- field-programmable gate array
Publisher's Copyright Statement
- This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/
Fingerprint
Dive into the research topics of 'Real-time field-programmable gate array-based closed-loop deep brain stimulation platform targeting cerebellar circuitry rescues motor deficits in a mouse model of cerebellar ataxia'. Together they form a unique fingerprint.Projects
- 2 Finished
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ITF: Therapeutic Potential of a Novel Deep Brain Stimulation Target Site And Neural Prosthetic Device For Treating Parkinson’s Disease
MA, C. H. E. (Principal Investigator / Project Coordinator), KUMAR, G. (Co-Investigator) & TIN, C. (Co-Investigator)
1/07/20 → 31/08/22
Project: Research
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ITF: Therapeutic Potential Of Neural Motor Prostheses Device For The Treatment Of Spinocerebellar Ataxia
MA, C. H. E. (Principal Investigator / Project Coordinator), KUMAR, G. (Co-Investigator) & TIN, C. (Co-Investigator)
1/01/18 → 30/06/19
Project: Research
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