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DOI 10.1159/000548796

Медицинская библиотека · Journal of vascular research · 2026

Differential Blood-Brain Barrier Permeability Driven by Asymmetric Hypoperfusion in a Vascular Dementia Model.

Dai Mengjun, Qu Kuizhi, Jiang Ying, Gao Song, Rui Yan-Ning, Xu Zhen

СтатьяСравнительное исследованиеПеревод пока не подготовлен

Аннотация

INTRODUCTION

Blood-brain barrier (BBB) dysfunction has been associated with vascular dementia (VaD). However, the underlying mechanisms causing BBB dysfunction remain unclear, especially regarding cerebral hypoperfusion. This study aimed to investigate the effects of asymmetric hypoperfusion on BBB permeability using a mouse model of VaD.

METHODS

Asymmetric bilateral common carotid artery stenosis (ACAS) was induced using ligature rings. BBB integrity was assessed on 3 days post-surgery using Evans blue, IgG, and albumin extravasation. A modified tissue processing protocol optimized endogenous marker detection. Regional and sex-based differences in BBB permeability were analyzed.

RESULTS

Increased BBB permeability was observed in both corpus callosum and cortical areas, with significantly more severe leakage in the left cortex compared to the right, correlating directly with lower cerebral blood flow on the left side. In contrast, no significant asymmetrical difference in BBB permeability was detected in the corpus callosum. Additionally, male and female mice exhibited similar patterns of BBB permeability.

CONCLUSION

This study provides the first evidence that asymmetrical hypoperfusion significantly impacts regional BBB permeability in a mouse model of VaD. These findings highlight the importance of local hemodynamic changes in driving BBB dysfunction and underscore potential therapeutic targets for preventing or mitigating VaD progression.

Для цитирования: Dai Mengjun, Qu Kuizhi, Jiang Ying, Gao Song, Rui Yan-Ning, Xu Zhen. Differential Blood-Brain Barrier Permeability Driven by Asymmetric Hypoperfusion in a Vascular Dementia Model.. Journal of vascular research. 2026. DOI: 10.1159/000548796.

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