Prolonged Central Thalamic Intermittent Theta-Burst Stimulation Rescued Memory Deficits in Alzheimer's Disease Mouse Model
Motivation: Addressing the global AD crisis by investigating CT-iTBS as a non-pharmacological treatment to enhance memory and cognition. Goal(s): To explore the therapeutic efficacy and determine the optimal treatment protocol of CT-iTBS in AD while unveiling its potential underlying mechanism for enhancing memory and cognitive functions. Approach: Utilized brain magnetic resonance imaging analysis, behavioral tests, and immunofluorescence staining for assessing the therapeutic effect of different durations of CT-iTBS treatment. Results: Prolonged CT-iTBS significantly enhanced cognitive and memory behaviors, altered brain functional connectivity, promoted a neuroprotective effect, and reduced amyloid accumulation in AD mouse model. These findings present a promising therapeutic avenue for AD patients. Impact: Our findings revealed a highly promising avenue for enhancing the quality of life for individuals with AD and provided insights into the potential underlying neuroprotective mechanisms of CT-iTBS in alleviating memory deficits.
Authors
- You‐Yin Chen (ORCID: https://orcid.org/0000-0003-4869-3857)
- Yi-Chun Lee (ORCID: https://orcid.org/0000-0002-6826-7049)
- Ting-Chieh Chen
- Ssu‐Ju Li (ORCID: https://orcid.org/0000-0001-9686-058X)
- Yu‐Chun Lo (ORCID: https://orcid.org/0000-0002-3595-5291)
- Yunting Liu (ORCID: https://orcid.org/0000-0003-3799-0362)
- Yao‐Wen Liang (ORCID: https://orcid.org/0009-0008-0112-5338)
- Ching-Wen Chang
- Sheng-Huang Lin
- Yi-Chen Lin
- Ching-Te Chen
Publication Details
- Journal
- Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
- Published
- 2024-11-26
- DOI
- https://doi.org/10.58530/2024/0162
- Primary Topic
- Neurological disorders and treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00