关斯佳, 张琦, 祝欣欣, 曲爱娟. 过氧化物酶体增殖物激活受体α在代谢性心血管疾病中的研究进展J. 药学学报, 2025, 60(12): 3595-3604. DOI: 10.16438/j.0513-4870.2025-0920
引用本文: 关斯佳, 张琦, 祝欣欣, 曲爱娟. 过氧化物酶体增殖物激活受体α在代谢性心血管疾病中的研究进展J. 药学学报, 2025, 60(12): 3595-3604. DOI: 10.16438/j.0513-4870.2025-0920
GUAN Si-jia, ZHANG Qi, ZHU Xin-xin, QU Ai-juan. The role of peroxisome proliferator-activated receptor α in metabolic cardiovascular diseasesJ. Acta Pharmaceutica Sinica, 2025, 60(12): 3595-3604. DOI: 10.16438/j.0513-4870.2025-0920
Citation: GUAN Si-jia, ZHANG Qi, ZHU Xin-xin, QU Ai-juan. The role of peroxisome proliferator-activated receptor α in metabolic cardiovascular diseasesJ. Acta Pharmaceutica Sinica, 2025, 60(12): 3595-3604. DOI: 10.16438/j.0513-4870.2025-0920

过氧化物酶体增殖物激活受体α在代谢性心血管疾病中的研究进展

The role of peroxisome proliferator-activated receptor α in metabolic cardiovascular diseases

  • 摘要: 代谢性心血管疾病是一类由肥胖、高血压、代谢相关性脂肪性肝病(metabolic-associated fatty liver disease, MAFLD) 和糖尿病等代谢危险因素共同驱动的心血管疾病, 其发生发展与代谢紊乱、炎症反应等病理过程密切相关。过氧化物酶体增殖物激活受体α (peroxisome proliferator-activated receptor α, PPARα) 作为核受体超家族成员, 对维持机体代谢稳态至关重要。近年研究表明, PPARα可通过调控机体脂质代谢、抑制炎症及氧化应激等, 在代谢性心血管疾病中发挥保护作用。本文系统综述PPARα的分子结构及其生物学功能, 重点讨论其在代谢性心血管疾病中的作用机制, 并对PPARα激动剂在临床前研究与临床试验中的疗效及面临的挑战进行总结, 以期为代谢性心血管疾病防治提供理论依据和策略方向。

     

    Abstract: Metabolic cardiovascular diseases are a category of cardiovascular conditions driven by metabolic risk factors, such as obesity, hypertension, metabolic-associated fatty liver disease (MAFLD), and diabetes, in which metabolism disturbance and inflammatory responses are key contributors. Peroxisome proliferator-activated receptor α (PPARα), a member of the nuclear receptor superfamily, plays a critical role in the maintenance of metabolic homeostasis. Recent studies have indicated that PPARα exerts beneficial effects on metabolic cardiovascular diseases via regulating lipid metabolism, inflammatory responses, and mitigating oxidative stress. This review summarized the molecular structure and biological functions of PPARα, with a focus on the underlying mechanisms in PPARα regulating metabolic cardiovascular diseases and translational significance of PPARα agonists in preclinical-clinical studies, aiming to establish novel therapeutic paradigms for these disorders.​

     

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