Sex differences in the sleep architecture and sleep-disordered breathing in C57BL/6J mice

高碳酸血症 医学 容积描记器 呼吸暂停 缺氧(环境) 睡眠呼吸暂停 呼吸系统 通风(建筑) 睡眠(系统调用) 多导睡眠图 阻塞性睡眠呼吸暂停 内科学 麻醉 颈动脉体 呼吸 生理学 缺氧通气反应 睡眠阶段 高氧 呼吸控制 内分泌学 性别特征 外围设备 周期性呼吸 呼吸暂停-低通气指数 激素 睡眠和呼吸 心脏病学 呼吸 呼吸分钟容积 呼吸道疾病 通气不足 睡眠研究 快速眼动睡眠 呼吸频率 间歇性缺氧
作者
Dashdulam Davaanyam,Luu V. Pham,Huy Pho,Noah R Williams,Vsevolod Y. Polotsky,Lenise Jihe Kim
出处
期刊:Sleep [Oxford University Press]
标识
DOI:10.1093/sleep/zsag176
摘要

STUDY OBJECTIVES: Sex differences in sleep disorders have been reported. Sleep disordered-breathing (SDB) is more prevalent in men, whereas women are more prone to insomnia. Mouse models have been extensively used in sleep research, but sex differences are not routinely taken into account. We performed a comprehensive examination of sleep architecture, breathing during sleep, and chemosensitivity in male and female C57BL/6 J mice. METHODS: Mice instrumented with EEG/EMG electrodes underwent full-polysomnography inside a whole-body plethysmography chamber. Ventilatory responses to hypoxia (10% O2, 3% CO2) and to two regimens of hypercapnia (8% CO2 balanced in 20.9% O2 vs 8% CO2 balanced in 65% O2) were measured. Female mice underwent bilateral ovariectomy (OVX) and repeated the assessments. RESULTS: Female mice showed more frequent arousals from sleep, increased apnea frequency and increased respiratory variability compared to males. Hypoxic chemoreflex did not differ between sexes, but CO2 chemosensitivity was significantly augmented in females. The carotid body inactivation by hyperoxia attenuated CO2 chemoreflex responses in females, but not in males. OVX reduced CO2 chemosensitivity, but did not affect respiratory variability, while the apnea index increased. CONCLUSIONS: In C57BL/6 J mice, we found significant sex differences in sleep. Females manifested a more severe SDB phenotype characterized by more frequent arousals and heightened CO2 responsiveness compared to males. Our findings also suggested that more robust peripheral CO2 chemoreflexes may account for sleep disruptions in female mice. Our findings further implicate ovarian hormones in respiratory control.
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