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Effect of Yokukansan on sleep disturbance in a rat model of cerebrovascular dementia
Author(s) -
Nagao Masaki,
Takasaki Kotaro,
Nogami Ai,
Hirai Yuko,
Moriyama Hiroshi,
Uchida Naoki,
Kubota Kaori,
Katsurabayashi Shutaro,
Mishima Kenichi,
Nishimura Ryoji,
Iwasaki Katsunori
Publication year - 2014
Publication title -
traditional and kampo medicine
Language(s) - English
Resource type - Journals
ISSN - 2053-4515
DOI - 10.1002/tkm2.1008
Subject(s) - non rapid eye movement sleep , wakefulness , sleep disorder , anesthesia , prefrontal cortex , neuroscience of sleep , dementia , medicine , psychology , neuroscience , electroencephalography , cognition , disease
Aim Symptoms of dementia are classified into cognitive dysfunction and behavioral and psychological symptoms of dementia, including sleep disturbance. Yokukansan ( YKS ) is effective for sleep disturbance in patients with dementia, but the mechanisms are still unclear. In this study, we evaluated sleep disturbance in rats with cerebral ischemia. We investigated the effect of YKS on sleep disturbance in cerebral ischemia‐treated rats. Methods Cerebral ischemia was induced by twice occluding both of the common carotid arteries. Wakefulness, non‐rapid eye movement ( NREM ) sleep, and rapid eye movement ( REM ) sleep were classified using electroencephalography and electromyography. mRNA expression of sleep–wakefulness signals were quantified using reverse transcription–polymerase chain reaction. Results Rats with cerebral ischemia had a higher total wakefulness time and lower total NREM sleep time during the light phase. These changes were ameliorated with 1000 mg/kg YKS for 14 days, but not 3 mg/kg donepezil for 7 days. mRNA expression of the prefrontal cortical prostaglandin ( PG ) E 2 ( EP4 ) receptor and of the PGD 2 ( DP ) receptor was increased by cerebral ischemia. Elevated prefrontal cortical EP4 and DP receptor mRNA expression was reduced by YKS treatment. Conclusion Rats with cerebral ischemia had NREM sleep disturbance. YKS might reduce this sleep disturbance by preventing neuroinflammation, and this was mediated by the EP4 and DP receptors in the prefrontal cortex.