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衰老相关的微血管内皮功能障碍:关注血脑和血视网膜屏障。

Senescence-associated microvascular endothelial dysfunction: A focus on the blood-brain and blood-retinal barriers.

机构信息

Department of Biochemistry, Konkuk University School of Medicine, Republic of Korea; Research Institute of Medical Science, Konkuk University, Republic of Korea; IBST, Konkuk University, Republic of Korea.

Department of Biochemistry, Konkuk University School of Medicine, Republic of Korea.

出版信息

Ageing Res Rev. 2024 Sep;100:102446. doi: 10.1016/j.arr.2024.102446. Epub 2024 Aug 5.

Abstract

The blood-brain barrier (BBB) and blood-retinal barrier (BRB) constitute critical physiochemical interfaces, precisely orchestrating the bidirectional communication between the brain/retina and blood. Increased permeability or leakage of these barriers has been demonstrably linked to age-related vascular and parenchymal damage. While it has been suggested that the gradual aging process may coincide with disruptions in these barriers, this phenomenon is significantly exacerbated in individuals with age-related neurodegenerative disorders (ARND). This review focuses on the microvascular endothelium, a key constituent of BBB and BRB, highlighting the impact of endothelial senescence on barrier dysfunction and exploring recent discoveries regarding core pathways implicated in its breakdown. Subsequently, we address the "vascular senescence hypothesis" for ARND, with a particular emphasis on Alzheimer's disease and age-related macular degeneration, centered on endothelial senescence. Finally, we discuss potential senotherapeutic strategies targeting barrier dysfunction.

摘要

血脑屏障(BBB)和血视网膜屏障(BRB)构成了关键的生理化学界面,精确地协调着大脑/视网膜和血液之间的双向通讯。这些屏障的通透性或渗漏增加已经被证明与年龄相关的血管和实质损伤有关。虽然有人认为,随着年龄的增长,这个过程可能会导致这些屏障的破坏,但在与年龄相关的神经退行性疾病(ARND)患者中,这种现象会显著加剧。本综述重点关注微血管内皮细胞,它是 BBB 和 BRB 的关键组成部分,强调内皮细胞衰老对屏障功能障碍的影响,并探讨了与内皮细胞破坏有关的核心途径的最新发现。随后,我们探讨了 ARND 的“血管衰老假说”,特别关注以内皮细胞衰老为中心的阿尔茨海默病和年龄相关性黄斑变性。最后,我们讨论了针对屏障功能障碍的潜在衰老治疗策略。

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