老化和流体剪切应激对血管内皮代谢和动脉样硬化的影响
Wei-Li Wang1, Yu-Tsung Shih2, Shu-Yi Wei1
1Institute of Cellular and System Medicine, National Health Research Institutes, Miaoli, Taiwan.
Journal of biomedical science
|September 2, 2025
概括
衰老会影响内皮细胞的新陈代谢,从而促进动脉样硬化. 本综述探讨了EC中与年龄相关的代谢变化及其在心血管疾病发展中的作用以及潜在的治疗点.
科学领域:
- 心血管生物学
- 内皮细胞代谢
- 老龄化研究
背景情况:
- 衰老是代谢综合征和动脉样硬化的主要危险因素,
- 内皮细胞 (ECs) 对于血管平衡至关重要,其功能障碍,包括障碍功能和炎症,启动动动脉形成.
- 由于衰老和血动力学因素,例如剪切压力,导致EC代谢发生显著改变,影响血管健康.
研究的目的:
- 审查与年龄相关的代谢重编程的最新进展.
- 阐明EC代谢功能障碍对动脉样硬化的贡献.
- 讨论EC新陈代谢和潜在治疗策略的方法.
主要方法:
- 对内皮细胞代谢,衰老和动脉样硬化的当前文献的综述.
- 分析液体剪切应力对EC代谢途径的影响.
- 探索年龄引起的代谢变化,包括糖解,脂肪酸,氨基酸代谢和线粒体呼吸.
主要成果:
- 衰老驱动了ECs的深度代谢重编程,包括破坏糖分和线粒体功能障碍.
- 在衰老的血管系统中,扰乱的振荡剪切应力 (OS) 促进了动脉动脉信号传递和EC炎症.
- 受年龄和剪切压力影响的EC的代谢失调是EC功能障碍和动脉样硬化的关键驱动因素.
结论:
- 内皮细胞代谢是与年龄相关的动脉样硬化的关键因素,但尚未得到充分研究.
- 向EC代谢途径为预防或延缓动脉样硬化提供了一个有前途的治疗途径.
- 了解EC代谢重编程对于开发抗老年性心血管疾病的新策略至关重要.
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