Dong Menglu, Liang Xili, Zhu Tian, Xu Ting, Xie Liwei, Feng Yuan
Sleep Medicine Center, Department of Psychiatric, Nanfang Hospital, Southern Medical University, Guangzhou, People's Republic of China.
Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, State Key Laboratory of Applied Microbiology Southern China, Institute of Microbiology, Guangdong Academy of Sciences, Guangzhou, People's Republic of China.
Nat Sci Sleep. 2024 May 25;16:517-530. doi: 10.2147/NSS.S454297. eCollection 2024.
Obstructive sleep apnea (OSA) is a prevalent sleep breathing disorder characterized by intermittent hypoxia (IH), with continuous positive airway pressure (CPAP) as its standard treatment. However, the effects of intermittent hypoxia/reoxygenation (IH/R) on weight regulation in obesity and its underlying mechanism remain unclear. Gut microbiota has gained attention for its strong association with various diseases. This study aims to explore the combined influence of IH and obesity on gut microbiota and to investigate the impact of reoxygenation on IH-induced alterations.
Diet-induced obese (DIO) rats were created by 8-week high-fat diet (HFD) feeding and randomly assigned into three groups (n=15 per group): normoxia (NM), IH (6% O, 30 cycles/h, 8 h/day, 4 weeks), or hypoxia/reoxygenation (HR, 2-week IH followed by 2-week reoxygenation) management. After modeling and exposure, body weight and biochemical indicators were measured, and fecal samples were collected for 16S rRNA sequencing.
DIO rats in the IH group showed increased weight gain (p=0.0016) and elevated systemic inflammation, including IL-6 (p=0.0070) and leptin (p=0.0004). Moreover, IH rats exhibited greater microbial diversity (p<0.0167), and significant alterations in the microbial structure (p=0.014), notably the order , accompanied by an upregulation of bile acid metabolism predicted pathway (p=0.0043). Reoxygenation not only improved IH-exacerbated obesity, systemic inflammation, leptin resistance, and sympathetic activation, but also showed the potential to restore IH-induced microbial alterations. Elevated leptin levels were associated with (p=0.0008) and (p=0.0019), while body weight was linked to (p=0.0377). Additionally, the abundance of was negatively correlated with leptin levels (p=0.0006) and weight (p=0.0339).
IH leads to gut dysbiosis and metabolic disorders, while reoxygenation therapy demonstrates a potentially protective effect by restoring gut homeostasis and mitigating inflammation. It highlights the potential benefits of CPAP in reducing metabolic risk among obese patients with OSA.
阻塞性睡眠呼吸暂停(OSA)是一种常见的睡眠呼吸障碍,其特征为间歇性缺氧(IH),持续气道正压通气(CPAP)是其标准治疗方法。然而,间歇性缺氧/复氧(IH/R)对肥胖患者体重调节的影响及其潜在机制仍不清楚。肠道微生物群因其与多种疾病的密切关联而受到关注。本研究旨在探讨IH和肥胖对肠道微生物群的综合影响,并研究复氧对IH诱导变化的影响。
通过8周高脂饮食(HFD)喂养建立饮食诱导肥胖(DIO)大鼠,并随机分为三组(每组n = 15):常氧(NM)、IH(6%氧气,30次循环/小时,8小时/天,4周)或缺氧/复氧(HR,2周IH后2周复氧)处理。建模和暴露后,测量体重和生化指标,并收集粪便样本进行16S rRNA测序。
IH组的DIO大鼠体重增加(p = 0.0016),全身炎症升高,包括白细胞介素-6(IL-6,p = 0.0070)和瘦素(p = 0.0004)。此外,IH大鼠表现出更大的微生物多样性(p < 0.0167),微生物结构有显著改变(p = 0.014),特别是 目,同时胆汁酸代谢预测途径上调(p = 0.0043)。复氧不仅改善了IH加重的肥胖、全身炎症、瘦素抵抗和交感神经激活,还显示出恢复IH诱导的微生物改变的潜力。瘦素水平升高与 (p = 0.0008)和 (p = 0.0019)相关,而体重与 (p = 0.0377)相关。此外, 的丰度与瘦素水平(p = 0.0006)和体重(p = 0.0339)呈负相关。
IH导致肠道菌群失调和代谢紊乱,而复氧疗法通过恢复肠道稳态和减轻炎症显示出潜在的保护作用。这突出了CPAP在降低肥胖OSA患者代谢风险方面的潜在益处。