Electroacupuncture ameliorates blood-brain barrier disruption after ischemic stroke through histone acetylation regulation at the matrix metalloproteinase 9 and tissue inhibitor of metalloproteinase 2 genes

被引:0
作者
Chen, Yonglin [1 ]
Ling, Ouyang [1 ]
Meng, Lingling [1 ]
Wu, Bufan [1 ]
Peng, Rou [1 ]
Liu, Sitong [1 ]
Hou, Dan [1 ]
Wang, Yaling [1 ]
Jing, Xinyue [1 ]
Lu, Shengfeng [1 ]
Fu, Shuping [1 ]
机构
[1] Univ Chinese Med, Minist Educ, Key Lab Acupuncture & Med Res, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
blood-brain barrier; matrix metalloproteinase 9; tissue inhibitor of metalloproteinases; electroacupuncture; histone acetylation; TIGHT JUNCTION PROTEINS; CEREBRAL-ISCHEMIA; MATRIX METALLOPROTEINASES; RAT MODEL; FUNCTIONAL RECOVERY; REPERFUSION; EXPRESSION; MMP-9; INJURY; ANGIOGENESIS;
D O I
10.19852/j.cnki.jtcm.20240610.004
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
OBJECTIVE: To explore whether the regulation of matrix metalloproteinase 9 (MMP-9)/ tissue inhibitors of MMPs (TIMPs) gene expression through histone acetylation is a possible mechanism by which electroacupuncture (EA) protects blood-brain barrier (BBB) integrity in a middle cerebral artery occlusion (MCAO) rat model. METHODS: Male Sprague-Dawley rats were divided into four groups: the sham group, the MCAO group, the MCAO + EA (MEA) group, and the MCAO + EA + HAT inhibitor (HATi) group. The MCAO model was generated by blocking the middle cerebral artery. EA was applied to Baihui (GV20). Samples were collected 1 or 3 d after reperfusion. Neurological function scores and Evans blue extravasation were employed to evaluate the poststroke injury. The effect of EA on MMP-9/TIMPs gene expression was assessed by real-time fluorescence quantitative polymerase chain reaction (RT-qPCR) and chromatin immunoprecipitation (ChIP). RESULTS: Our results showed that EA treatment prominently improved neurological function and ameliorated BBB disruption. The RT-qPCR assay showed that EA reduced the expression of MMP-9 and promoted TIMP-2 mRNA expression, but HATi reversed these effects of EA. In addition, ChIP results revealed that EA decreased the enrichment of H3K9ace/H3K27ace at MMP-9 promoters and notably stimulated the recruitment of H3K9ace/H3K27ace at TIMP-2 promoter. CONCLUSION: EA treatment at Baihui (GV20) regulates the transcription of MMP-9 and TIMP-2 through histone acetylation modification in the acute stage of stroke, which preserves the structural integrity of the BBB in MCAO rats. These findings suggested that the histone acetylation-mediated transcriptional activity of target genes may be a crucial mechanism of EA treatment in stroke.
引用
收藏
页码:734 / 744
页数:11
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