Ningzhi Zhang, Feng Wei, Sisi Ning, Jialu Hu, Hongtao Shi, Zhifeng Yao, Minna Tang, Yongqiao Zhang, Jiaxin Gong, Junbo Ge, Zhaoqiang Cui
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引用次数: 0
Abstract
The increased incidence of hypertension associated with obstructive sleep apnea (OSA) presents significant physical, psychological, and economic challenges. Peroxisome proliferator-activated receptor gamma (PPARγ) plays a role in both OSA and hypertension, yet the therapeutic potential of PPARγ agonists and antagonists for OSA-related hypertension remains unexplored. Therefore, we constructed a chronic intermittent hypoxia (CIH)-induced hypertension rat model that mimics the pathogenesis of OSA-related hypertension in humans. The model involved administering PPARγ agonist rosiglitazone (RSG), PPARγ antagonist GW9662, or normal saline, followed by regular monitoring of blood pressure and thoracic aorta analysis using staining and electron microscopy. Intriguingly, our results indicated that both RSG and GW9662 appeared to potently counteract CIH-induced hypertension. In silico study suggested that GW9662's antihypertensive effect might mediated through angiotensin II receptor type 1 (AGTR1). Our findings provide insights into the mechanisms of OSA-related hypertension and propose novel therapeutic targets.
与阻塞性睡眠呼吸暂停(OSA)相关的高血压发病率的增加带来了巨大的生理、心理和经济挑战。过氧化物酶体增殖激活受体γ(PPARγ)在 OSA 和高血压中都起着作用,但 PPARγ 激动剂和拮抗剂对 OSA 相关高血压的治疗潜力仍有待探索。因此,我们建立了慢性间歇性缺氧(CIH)诱导的高血压大鼠模型,该模型模拟了人类 OSA 相关高血压的发病机制。该模型包括给予 PPARγ 激动剂罗格列酮 (RSG)、PPARγ 拮抗剂 GW9662 或生理盐水,然后定期监测血压并使用染色和电子显微镜分析胸主动脉。有趣的是,我们的研究结果表明,RSG 和 GW9662 似乎都能有效对抗 CIH 诱导的高血压。硅学研究表明,GW9662 的抗高血压作用可能是通过血管紧张素 II 受体 1 型(AGTR1)介导的。我们的研究结果揭示了 OSA 相关高血压的发病机制,并提出了新的治疗靶点。