华中科技大学学报(医学版) ›› 2026, Vol. 55 ›› Issue (5): 752-758.doi: 10.3870/j.issn.1672-0741.25.10.012

• 综述 • 上一篇    下一篇

过氧化物酶体增殖物激活受体δ在血管重构中的作用机制研究进展*

唐溪涓, 贺立群△   

  1. 华中科技大学同济医学院附属武汉中西医结合医院心血管内科,武汉 430022
  • 收稿日期:2025-10-10 发布日期:2026-10-30
  • 通讯作者: △E-mail:liqunhe0902@hust.edu.cn
  • 作者简介:唐溪涓,女,1999年生,医学硕士,住院医师,E-mail:ttt_132@hust.edu.cn
  • 基金资助:
    *湖北省卫生健康委科研项目(No. WJ2023F043)

Mechanisms of Peroxisome Proliferator-Activated Receptor δ in Vascular Remodeling

Tang Xijuan, He Liqun△   

  1. Department of Cardiology, Traditional Chinese and Western Medicine Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022
  • Received:2025-10-10 Published:2026-10-30
  • Contact: △E-mail:liqunhe0902@hust.edu.cn

摘要: 血管重构是诸多心血管疾病的核心病理环节,过氧化物酶体增殖物激活受体δ(PPARδ)作为核受体家族的重要成员,不仅在调控能量代谢、炎症反应、氧化应激等生理过程中发挥重要作用,还通过调控血管平滑肌细胞增殖迁移、细胞外基质重塑等多种复杂病理生理过程来影响血管重构进程。深入研究PPARδ在血管重构中的具体作用机制,有助于揭示心血管疾病的发病机制,发现新的干预靶点,从而降低心血管事件风险,改善患者预后。该文对PPARδ的结构、功能以及近年来其在血管重构过程中的作用及机制相关研究进行综述,以期为心血管疾病提供新的治疗靶点。

关键词: 过氧化物酶体增殖物激活受体δ, 血管重构, 氧化应激, 血管平滑肌细胞, 巨噬细胞

Abstract: Vascular remodeling is a pivotal pathological process in numerous cardiovascular diseases. Peroxisome proliferator-activated receptor delta (PPARδ), a key member of the nuclear receptor family, not only plays a crucial role in regulating physiological processes such as energy metabolism, inflammatory responses, and oxidative stress, but also influences the vascular remodeling process by modulating various complex pathophysiological mechanisms, including the proliferation and migration of vascular smooth muscle cells and extracellular matrix remodeling. In-depth exploration of the specific mechanisms by which PPARδ affects vascular remodeling can help elucidate the pathogenesis of cardiovascular diseases, identifying novel intervention targets, mitigating the risk of cardiovascular events, and improving patient prognosis. This article reviews the structure and function of PPARδ and its recent research on the impact and mechanisms in vascular remodeling, aiming to offer new therapeutic targets for cardiovascular diseases.

Key words: PPARδ, vascular remodeling, oxidative stress, vascular smooth muscle cells, macrophages

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