内皮衰老及其对阿尔茨海默氏病血管生成的影响
Irina Georgieva1, Jana Tchekalarova2, Dimitar Iliev3
1Institute of Biophysics and Biomedical Engineering, Bulgarian Academy of Sciences, Acad. George Bonchev, Str. Bl. 21, 1113 Sofia, Bulgaria.
International journal of molecular sciences
|July 29, 2023
概括
细胞衰老和氧化应激会破坏血管形成 (血管生成),导致衰老和阿尔茨海默病. 像运动这样的生活方式干预措施可能会带来治疗效益.
科学领域:
- 血管生物学 血管生物学
- 神经科学是一个神经科学.
- 衰老研究研究 衰老研究
背景情况:
- 内皮细胞由于环境压力而经历衰老和亡.
- 改变血管功能会影响血管生成和内皮健康,导致与年龄相关的疾病.
- 大脑的健康取决于血管的完整性和营养供应.
研究的目的:
- 审查衰老中的衰老,氧化应激,细胞外囊泡和细胞外矩阵的相互作用.
- 强调血管新生在衰老和阿尔茨海默氏症 (AD) 中的作用.
- 探索调节血管生成和血管衰老的治疗策略.
主要方法:
- 现有文献的叙述性审查.
- 对内皮衰老与血管生成之间的关系进行分析.
- 在AD相关的血管生成中讨论信号通路 (Delta-Notch,VEGF).
主要成果:
- 血管新生受损,以失调和泄漏为特征,有助于神经退行.
- 在AD中失调的血管生成与改变的Delta-Notch和VEGF信号联系在一起.
- 细胞外囊泡在衰老中发挥作用,并可能作为AD生物标志物.
结论:
- 内皮衰老和血管生成中断是衰老和AD等神经退行性疾病的关键因素.
- 针对血管新生和血管衰老的治疗干预措施,如运动和热量限制,显示出希望.
- 对细胞外囊泡的进一步研究可能会产生早期AD检测方法.
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