PI3K/AKT/mTOR通路
半影
医学
蛋白激酶B
缺血
埃文斯蓝
血脑屏障
信号转导
药理学
脑缺血
神经保护
冲程(发动机)
污渍
炎症
内科学
化学
细胞生物学
中枢神经系统
生物
机械工程
生物化学
基因
工程类
作者
Guangxiao Ni,Lulu Kou,Chun-Qiao Duan,Ran Meng,Pu Wang
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2024-09-20
卷期号:19 (9): e0306793-e0306793
标识
DOI:10.1371/journal.pone.0306793
摘要
Objective To explore whether miR-199a-5p regulated BBB integrity through PI3K/Akt pathway after ischemia stroke. Methods Adult male Sprague-Dawley rats with permanent middle cerebral artery occlusion(MCAO) were used in experiment. The Ludmila Belayev 12-point scoring was used to measure the neurological function of MCAO rats. The Evans Blue Stain, immunofluorescence staining, western-blotting and RT-PCR were performed to evaluate the effects of miR-199a-5p mimic on BBB integrity in rats following MCAO. Results The result suggested that miR-199a-5p mimic treatment possessed the potential to boost proprioception and motor activity of MCAO rats. MiR-199a-5p decreased the expression of PIK3R2 after MCAO, activated Akt signaling pathway, and increased the expression of Claudin-5 and VEGF in the ischemic penumbra. Furthermore, miR-199a-5p alleviated inflammation after cerebral ischemia. BBB leakage and neurocyte apoptosis were cut down in MCAO rats treated with miR-199a-5p mimic. Conclusions MiR-199a-5p mimic decreased the expression of PIK3R2 and activated Akt signaling pathway after ischemia stroke, reduced the expression of inflammatory cytokines, and attenuated BBB disruption after ischemic stroke.
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