| Literature DB >> 25118620 |
Masatoshi Sato1, Yohei Sagawa1, Nobuhide Hirai2, Shinichi Sato3, Masashi Okuro4, Samika Kumar2, Takashi Kanbayashi5, Tetsuo Shimizu5, Noriaki Sakai2, Seiji Nishino6.
Abstract
Sleep and behavioral monitoring of young mice is necessary for understating the progress of symptoms in congenital and acquired diseases associated with sleep and movement disorders. In the current study, we have developed a non-invasive sleep monitoring system that identifies wake and sleep patterns of newborn mice using a simple piezoelectric transducer (PZT). Using this system, we have succeeded in detecting age-dependent occurrences and changes in sleep fragmentation of orexin/ataxin-3 narcoleptic mice (a narcoleptic mouse model with postnatal hypocretin/orexin cell death) across the disease onset. We also detected REM sleep/cataplexy patterns (i.e., immobility with clear heartbeat [IMHB] signals due to the flaccid posture) by the PZT system, and found that sudden onset of REM sleep-like episodes specifically occur in narcoleptic, but not in wild type mice, suggesting that these episodes are likely cataplexy. In contrast, gradual onset of IMHB likely reflects occurrence of REM sleep. In summary, we have shown that the PZT system is useful as a non-invasive sleep and behavior monitoring system to analyze the developmental aspects of sleep and movement disorders in mice models.Entities:
Keywords: Cataplexy; Disease onset; Hypocretin/orexin; Mice; Narcolepsy; Piezoelectric system; REM sleep
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Year: 2014 PMID: 25118620 PMCID: PMC4648267 DOI: 10.1016/j.expneurol.2014.08.004
Source DB: PubMed Journal: Exp Neurol ISSN: 0014-4886 Impact factor: 5.330