Abstract
Disrupted sleep has a profound adverse impact on lives of Parkinson’s disease (PD) patients and their caregivers. Sleep disturbances are exceedingly common in PD, with substantial heterogeneity in type, timing, and severity. Among the most common sleep-related symptoms reported by PD patients are insomnia, excessive daytime sleepiness, and sleep fragmentation, characterized by interruptions and decreased continuity of sleep. Alterations in brain wave activity, as measured on the electroencephalogram (EEG), also occur in PD, with changes in the pattern and relative contributions of different frequency bands of the EEG spectrum to overall EEG activity in different vigilance states consistently observed. The mechanisms underlying these PD-associated sleep-wake abnormalities are poorly understood, and they are ineffectively treated by conventional PD therapies. To help fill this gap in knowledge, a new progressive model of PD – the MCI-Park mouse – was studied. Near the transition to the parkinsonian state, these mice exhibited significantly altered sleep-wake regulation, including increased wakefulness, decreased non-rapid eye movement (NREM) sleep, increased sleep fragmentation, reduced rapid eye movement (REM) sleep, and altered EEG activity patterns. These sleep-wake abnormalities resemble those identified in PD patients. Thus, this model may help elucidate the circuit mechanisms underlying sleep disruption in PD and identify targets for novel therapeutic approaches.
Original language | English (US) |
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Article number | 54 |
Journal | npj Parkinson's Disease |
Volume | 10 |
Issue number | 1 |
DOIs | |
State | Published - Dec 2024 |
Funding
This study was funded by Department of Defense grants W81XWH2110582 (F.W.T.) and W81XWH2110749 (D.J.S.), National Institute of Aging grant P01AG011412 (M.H.V., F.W.T.), Aligning Science Against Parkinson\u2019s (ASAP) grant 020551 (Y.D., D.J.S.), and the JPB Foundation (D.J.S.). The funders performed no role in study design, data collection, analysis or interpretation of data, the decision to publish, or writing of this manuscript. The authors would like to thank J. Sun, R. Xiang, C. Chen, and Y. Liu from the Dan laboratory for assistance in completing studies at University of California, Berkeley.
ASJC Scopus subject areas
- Neurology
- Clinical Neurology
- Cellular and Molecular Neuroscience