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老年大脑中的微血管衰竭:氧化应激,炎症和内皮衰退的融合途径
Jordana Mariane Neyra Chauca1, Maclovia Vázquez VanDyck1, Armando Espinoza Santana2
1Facultad de Medicina, Universidad Autónoma de Guadalajara, Guadalajara 45129, Mexico.
Biomedicines
|January 28, 2026
概括
衰老通过氧化应激,炎症和内皮衰老损害了微循环,影响了外围动脉疾病和大脑健康. 这种系统性问题影响了血脑屏障的完整性和神经血管功能.
科学领域:
- 血管生物学 血管生物学
- 衰老研究研究 衰老研究
- 神经科学是一个神经科学.
背景情况:
- 老化逐渐影响微循环系统,影响外周和脑血管的内皮稳定性.
- 氧化失衡,炎症和内皮疲劳会破坏微血管网络的稳定,将外围动脉疾病 (PAD) 与大脑功能障碍联系起来.
- 恶化的氧化还原稳定会损害内皮屏障功能和通信,促进神经血管损伤.
研究的目的:
- 审查氧化应激,炎症,内皮衰老和血脑屏障 (BBB) 破坏之间的相互作用的机械证据.
- 为了比较外围动脉疾病和大脑微循环病理,以确定共享的分子驱动因素.
- 了解衰老中内皮质恶化的全身机制.
主要方法:
- 叙述性审查整合实验,临床和翻译研究.
- 对外围动脉疾病和老化大脑循环的比较分析.
- 专注于将氧化应激,炎症,衰老和BBB完整性联系在一起的分子机制.
主要成果:
- 氧化应激会破坏线粒体功能,紧张的结节和血管生成.
- 炎症通过细胞因子激活和白细胞粘附来放大内皮功能障碍.
- 内皮衰老导致氧化的减少,毛细血管稀疏和屏障完整性的损害,这在PAD和老化大脑中很常见.
结论:
- 老化大脑中的微血管衰竭是系统性内皮质恶化的延伸.
- 共同的分子通路连接了外周和大脑的微循环功能障碍,表明了统一的衰老表型.
- 向内皮弹性和BBB完整性为老年人群提供治疗策略.
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