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DOI 10.1016/j.expneurol.2014.08.004

Медицинская библиотека · Experimental neurology · 2014

Noninvasive detection of sleep/wake changes and cataplexy-like behaviors in orexin/ataxin-3 transgenic narcoleptic mice across the disease onset.

Sato Masatoshi, Sagawa Yohei, Hirai Nobuhide, Sato Shinichi, Okuro Masashi, Kumar Samika, Kanbayashi Takashi, Shimizu Tetsuo, Sakai Noriaki, Nishino Seiji

СтатьяПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

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.

Для цитирования: Sato Masatoshi, Sagawa Yohei, Hirai Nobuhide, Sato Shinichi, Okuro Masashi, Kumar Samika, Kanbayashi Takashi, Shimizu Tetsuo, Sakai Noriaki, Nishino Seiji. Noninvasive detection of sleep/wake changes and cataplexy-like behaviors in orexin/ataxin-3 transgenic narcoleptic mice across the disease onset.. Experimental neurology. 2014. DOI: 10.1016/j.expneurol.2014.08.004.

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