Protective Effects of Xingnao Enema on Blood-brain Barrier Disruption in a Rat Model of Intracerebral Hemorrhage

被引:0
作者
Wang, Kun [1 ,2 ]
Cui, Yinglin [2 ]
Zhao, Xu [2 ]
Hu, Changjiang [1 ]
机构
[1] Chengdu Univ TCM, Dept Pharm, Chengdu 61137, Sichuan, Peoples R China
[2] Henan Univ TCM, Dept Clin Med Coll 2, Zhengzhou 450002, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Xingnao enema; Blood brain barrier; Intracerebral hemorrhage; Cerebral protection; TIGHT JUNCTION PROTEINS; SUBARACHNOID HEMORRHAGE; MATRIX-METALLOPROTEINASE-9; INHIBITION; APOPTOSIS; INJURY;
D O I
10.17582/journal.pjz/2019.51.6.2233.2243
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
Xingnao enema (XN) has been commonly used to treat intracerebral hemorrhage (ICH) in China with good therapeutic effect. As very little is known about the mechanism of action of XN, the purpose of this project was to investigate the neuroprotective effect of XN on ICH model rats and to explore the underlying mechanisms of this therapy. In this study, experimental ICH was induced by the administration of stereotaxic collagenase type VII into the caudate nucleus. XN (at a high dose and a low dose of 3.60g.kg(-1) and 1.80g.kg(-1), respectively) was administered via enema. The detection of neuronal apoptosis was measured by TUNEL assay. Using immunofluorescence, the expression of claudin-5, ZO-1 and VE-cadherin was detected. The expression of DNA methyltransferase 3b (DNMT3b) and Matrix metalloproteinase-9 (MMP-9) was evaluated by western blot. And microRNA-29b was identified using quantitative real-time PCR. 3). Compared with the Model group, the group treated with XN had a significantly reduced number of dead neurons in hippocampus and cortical regions of ICH rats. Furthermore, this treatment significantly increased protein expression of claudin-5, ZO-1 and VE-cadherin while protein expression of DNMT3b and MMP-9 were significantly inhibited. Finally, microRNA-29b level were also lower than the Model group. Our data suggests that XN has significant neuroprotective effects on the ICH model rats, which might help to protect the blood brain barrier by regulating of a cascade including the expression of microRNA-29b which regulates DNMT3b that in turn regulates level of MMP-9.
引用
收藏
页码:2233 / 2243
页数:11
相关论文
共 31 条
[1]   Astrocyte-endothelial interactions at the blood-brain barrier [J].
Abbott, NJ ;
Rönnbäck, L ;
Hansson, E .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (01) :41-53
[2]   Measuring serum matrix metalloproteinase-9 levels in peripheral blood after subarachnoid hemorrhage to predict cerebral vasospasm [J].
Akpinar, Aykut ;
Ucler, Necati ;
Erdogan, Uzay ;
Baydin, Serhat S. ;
Gungor, Abuzer ;
Tugcu, Bekir .
SPRINGERPLUS, 2016, 5
[3]   Pro-Inflammatory Mediators and Apoptosis Correlate to rt-PA Response in a Novel Mouse Model of Thromboembolic Stroke [J].
Ansar, Saema ;
Chatzikonstantinou, Eva ;
Thiagarajah, Rushani ;
Tritschler, Laurent ;
Fatar, Marc ;
Hennerici, Michael G. ;
Meairs, Stephen .
PLOS ONE, 2014, 9 (01)
[4]   The blood-brain barrier: an overview - Structure, regulation, and clinical implications [J].
Ballabh, P ;
Braun, A ;
Nedergaard, M .
NEUROBIOLOGY OF DISEASE, 2004, 16 (01) :1-13
[5]   Inhibition of c-Jun N-terminal kinase prevents blood-brain barrier disruption and normalizes the expression of tight junction proteins clautin-5 and ZO-1 in a rat model of subarachnoid hemorrhage [J].
Chen, Duo ;
Wei, Xiang-tai ;
Guan, Jun-hong ;
Yuan, Jiang-wei ;
Peng, Yu-tao ;
Song, Lei ;
Liu, Yun-hui .
ACTA NEUROCHIRURGICA, 2012, 154 (08) :1469-1476
[6]   Elevated Peripheral Neutrophils and Matrix Metalloproteinase 9 as Biomarkers of Functional Outcome Following Subarachnoid Hemorrhage [J].
Chou, S. H. -Y. ;
Feske, S. K. ;
Simmons, S. L. ;
Konigsberg, R. G. J. ;
Orzell, S. C. ;
Marckmann, A. ;
Bourget, G. ;
Bauer, D. J. ;
De Jager, P. L. ;
Du, R. ;
Arai, K. ;
Lo, E. H. ;
Ning, M. M. .
TRANSLATIONAL STROKE RESEARCH, 2011, 2 (04) :600-607
[7]  
Cui Y.L., 2000, LIAONING J TRADIT CH, V27, P364
[8]   Long-Lasting Cerebral Vasospasm, Microthrombosis, Apoptosis and Paravascular Alterations Associated with Neurological Deficits in a Mouse Model of Subarachnoid Hemorrhage [J].
El Amki, Mohamad ;
Dubois, Martine ;
Lefevre-Scelles, Antoine ;
Magne, Nicolas ;
Roussel, Melanie ;
Clavier, Thomas ;
Guichet, Pierre-Olivier ;
Gerardin, Emmanuel ;
Compere, Vincent ;
Castel, Helene .
MOLECULAR NEUROBIOLOGY, 2018, 55 (04) :2763-2779
[9]   MicroRNA-29 family reverts aberrant methylation in lung cancer by targeting DNA methyltransferases 3A and 3B [J].
Fabbri, Muller ;
Garzon, Ramiro ;
Cimmino, Amelia ;
Liu, Zhongfa ;
Zanesi, Nicola ;
Callegari, Elisa ;
Liu, Shujun ;
Alder, Hansjuerg ;
Costinean, Stefan ;
Fernandez-Cymering, Cecilia ;
Volinia, Stefano ;
Guler, Gulnur ;
Morrison, Carl D. ;
Chan, Kenneth K. ;
Marcucci, Guido ;
Calin, George A. ;
Huebner, Kay ;
Croce, Carlo M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (40) :15805-15810
[10]   Intracerebral Hemorrhage: A Common and Devastating Disease in Need of Better Treatment [J].
Fiorella, Dave ;
Zuckerman, Scott L. ;
Khan, Imad S. ;
Ganesh, Nishant K. ;
Mocco, J. .
WORLD NEUROSURGERY, 2015, 84 (04) :1136-1141