Division of Pulmonary and Critical Care Medicine, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Anesthesiology and Critical Care Medicine, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.
Sleep. 2023 Aug 14;46(8). doi: 10.1093/sleep/zsad158.
Obesity and male sex are main risk factors for sleep-disordered breathing (SDB). We have shown that male diet-induced obesity (DIO) mice develop hypoventilation, sleep apnea, and sleep fragmentation. The effects of DIO on breathing and sleep architecture in females have not been investigated. We hypothesized that female mice are less susceptible to the detrimental effects of DIO on sleep and SDB compared to males. Female DIO-C57BL/6J and lean C57BL/6J mice underwent 24-hour metabolic studies and were exposed to 8% CO2 to measure the hypercapnic ventilatory response (HCVR), and sleep studies. Ventilatory response to arousals was calculated as ratio of the average and peak minute ventilation (VE) during each arousal relative to the baseline VE. Breathing stability was measured with Poincaré plots of VE. Female obesity was associated with decreased metabolism, indicated by reduced oxygen consumption (VO2) and CO2 production (VCO2). VE in 8% CO2 and HCVR were significantly attenuated during wakefulness. NREM sleep duration was reduced in DIO mice, but REM sleep was preserved. Ventilation during NREM and REM sleep was augmented compared to lean mice. Arousal frequency was similar between groups. Obesity increased the frequency of spontaneous arousals, whereas the apnea index was 4-fold reduced in DIO compared to lean mice. Obesity decreased pre- and post-apnea arousals. Obese mice had more stable breathing with reduced ventilatory response to arousals, compared to lean females. We conclude that obese female mice are protected against SDB, which appears to be related to an attenuated CO2 responsiveness, compared to the lean state.
肥胖和男性性别是睡眠呼吸障碍(SDB)的主要危险因素。我们已经表明,雄性饮食诱导肥胖(DIO)小鼠会出现通气不足、睡眠呼吸暂停和睡眠片段化。DIO 对雌性呼吸和睡眠结构的影响尚未得到研究。我们假设与雄性相比,雌性小鼠对 DIO 对睡眠和 SDB 的有害影响的敏感性较低。雌性 DIO-C57BL/6J 和瘦 C57BL/6J 小鼠接受了 24 小时代谢研究,并暴露于 8%CO2 以测量高碳酸血症通气反应(HCVR)和睡眠研究。唤醒时的通气反应计算为每个唤醒期间平均和峰值分钟通气量(VE)与基线 VE 的比值。通过 VE 的 Poincaré 图测量呼吸稳定性。女性肥胖与代谢降低有关,表现为耗氧量(VO2)和二氧化碳产生量(VCO2)减少。清醒时,8%CO2 中的 VE 和 HCVR 明显减弱。DIO 小鼠的 NREM 睡眠时间减少,但 REM 睡眠得到保留。与瘦小鼠相比,NREM 和 REM 睡眠期间的通气增加。两组之间的唤醒频率相似。肥胖增加了自发唤醒的频率,而 DIO 小鼠的呼吸暂停指数比瘦小鼠低 4 倍。肥胖减少了呼吸暂停前和呼吸暂停后的唤醒。与瘦女性相比,肥胖小鼠的呼吸更稳定,对唤醒的通气反应降低。我们得出结论,肥胖雌性小鼠受到 SDB 的保护,这似乎与 CO2 反应性减弱有关,与瘦状态相比。