Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi, 214000, China.
Affiliated Hospital of Putian University, Putian, 351100, China.
Biomed Pharmacother. 2019 Apr;112:108580. doi: 10.1016/j.biopha.2019.01.041. Epub 2019 Feb 18.
Obstructive sleep apnea (OSA) and high salt content in modern diet has been particularly implicated in systemic hypertension, leading to increased morbidity and mortality. Gut dysbiosis, associated with increased risk of systemic immunological imbalance, plays a causal role in the development of cardiovascular diseases. Here, we investigated the effect of Lactobacillus rhamnosus GG strain (LGG) on the development of hypertension induced by OSA and high salt diet. In this study, hypertension was modeled in rats by feeding a high salt diet (HSD) for 6 wk and exposuring to chronic intermittent hypoxia (CIH) during the sleep cycle. We found that OSA combined with HSD increased the severity of hypertension through increasing level of blood Trimethylamine-Oxide (TMAO), release of Th1-related cytokine (IFN-γ) and inhibition of anti-inflammatory cytokine (TGF-β1), and affected the gut microbiome in rats, particularly by depleting Lactobacillus. In addition, expression of PERK1/2, PAkt and PmTOR increased in the aorta from rats with a CIH exposure and HSD. Consequently, treatment of model rats with LGG prevented aggravation of hypertension by reducing blood TMAO levels, modulating Th1/Th2 cytokine imbalance and suppressing phosphorylation levels of ERK1/2, Akt and mTOR. In line with these findings, our results connect high salt diet to the gut-immune axis and highlight the gut microbiome as a potential therapeutic target to counteract the development of OSA-induced hypertension basing on a high salt diet.
阻塞性睡眠呼吸暂停(OSA)和现代饮食中的高盐含量特别与系统性高血压有关,导致发病率和死亡率增加。与系统性免疫失衡风险增加相关的肠道菌群失调在心血管疾病的发展中起因果作用。在这里,我们研究了鼠李糖乳杆菌 GG 株(LGG)对 OSA 和高盐饮食引起的高血压发展的影响。在这项研究中,通过在睡眠周期中暴露于慢性间歇性缺氧(CIH)的同时用高盐饮食(HSD)喂养 6 周来在大鼠中建立高血压模型。我们发现,OSA 与 HSD 结合通过增加血液三甲胺氧化物(TMAO)水平、释放与 Th1 相关的细胞因子(IFN-γ)和抑制抗炎细胞因子(TGF-β1),从而加重高血压的严重程度,并影响大鼠的肠道微生物组,特别是通过消耗乳杆菌。此外,在接受 CIH 暴露和 HSD 的大鼠的主动脉中,PERK1/2、PAkt 和 PmTOR 的表达增加。因此,用 LGG 治疗模型大鼠可通过降低血液 TMAO 水平、调节 Th1/Th2 细胞因子失衡和抑制 ERK1/2、Akt 和 mTOR 的磷酸化水平来预防高血压的加重。与这些发现一致,我们的结果将高盐饮食与肠道-免疫轴联系起来,并强调肠道微生物组作为一种潜在的治疗靶点,以基于高盐饮食来对抗 OSA 引起的高血压的发展。