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探索缓解阻塞性睡眠呼吸暂停的药理机制:腺苷A2A受体对PI3K/Akt/HIF-1通路的下调作用(综述)

Exploring the pharmacological mechanisms for alleviating OSA: Adenosine A2A receptor downregulation of the PI3K/Akt/HIF‑1 pathway (Review).

作者信息

Ma Nini, Liu Peijie, Li Ning, Hu Yushi, Kang Liang

机构信息

School of Sports Medicine and Health, Chengdu Sport University, Chengdu, Sichuan 641418, P.R. China.

Institute of Sports Medicine and Health, Chengdu Sport University, Chengdu, Sichuan 641418, P.R. China.

出版信息

Biomed Rep. 2024 Nov 28;22(2):21. doi: 10.3892/br.2024.1899. eCollection 2025 Feb.

Abstract

Obstructive sleep apnea (OSA) is the most common type of sleep apnea, which leads to episodes of intermittent hypoxia due to obstruction of the upper airway. A key feature of OSA is the upregulation and stabilization of hypoxia-inducible factor 1 (HIF-1), a crucial metabolic regulator that facilitates rapid adaptation to changes in oxygen availability. Adenosine A2A receptor (A2AR), a major adenosine receptor, regulates HIF-1 under hypoxic conditions, exerting anti-inflammatory properties and affecting lipid metabolism. The present study explored the roles of A2AR in OSA regulation, specifically focusing on its effects via the PI3K/Akt/HIF-1 pathway. The findings enhance our understanding the pharmacological potential of A2AR in OSA management and suggest future research directions in exploring its clinical applications.

摘要

阻塞性睡眠呼吸暂停(OSA)是最常见的睡眠呼吸暂停类型,由于上呼吸道阻塞导致间歇性缺氧发作。OSA的一个关键特征是缺氧诱导因子1(HIF-1)的上调和稳定,HIF-1是一种关键的代谢调节因子,有助于快速适应氧供应的变化。腺苷A2A受体(A2AR)是主要的腺苷受体,在缺氧条件下调节HIF-1,具有抗炎特性并影响脂质代谢。本研究探讨了A2AR在OSA调节中的作用,特别关注其通过PI3K/Akt/HIF-1途径的作用。这些发现加深了我们对A2AR在OSA管理中的药理学潜力的理解,并为探索其临床应用提出了未来的研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2e2/11668141/c9a5f83cfd47/br-22-02-01899-g00.jpg

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