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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.
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1 Northwestern University, Department of Medicine, Feinberg School of Medicine, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, Center for Sleep & Circadian Biology, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507)
2 Northwestern University, Center for Sleep & Circadian Biology, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, Department of Neurobiology, Weinberg College of Arts and Sciences, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Bristol Myers Squibb, Neuroscience Discovery, Informatics and Predictive Sciences, Cambridge, USA (GRID:grid.419971.3) (ISNI:0000 0004 0374 8313)
3 Northwestern University, Department of Neuroscience, Feinberg School of Medicine, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla and CIBERNED, Instituto de Biomedicina de Sevilla, Seville, Spain (GRID:grid.414816.e) (ISNI:0000 0004 1773 7922)
4 University of California Berkeley, Department of Molecular & Cell Biology, Berkeley, USA (GRID:grid.47840.3f) (ISNI:0000 0001 2181 7878)
5 Northwestern University, Center for Sleep & Circadian Biology, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, Department of Neurobiology, Weinberg College of Arts and Sciences, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507)
6 University of California Berkeley, Department of Molecular & Cell Biology, Berkeley, USA (GRID:grid.47840.3f) (ISNI:0000 0001 2181 7878); Aligning Science Across Parkinson’s (ASAP) Collaborative Research Network, Chevy Chase, USA (GRID:grid.513948.2) (ISNI:0000 0005 0380 6410)
7 Northwestern University, Department of Neuroscience, Feinberg School of Medicine, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Aligning Science Across Parkinson’s (ASAP) Collaborative Research Network, Chevy Chase, USA (GRID:grid.513948.2) (ISNI:0000 0005 0380 6410)
8 Northwestern University, Center for Sleep & Circadian Biology, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, Department of Neurobiology, Weinberg College of Arts and Sciences, Evanston, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, The Ken & Ruth Davee Department of Neurology, Feinberg School of Medicine, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507); Northwestern University, Department of Psychiatry & Behavioral Sciences, Feinberg School of Medicine, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507)