Treatment with sodium orthovanadate reduces blood-brain barrier disruption via phosphatase and tensin homolog deleted on chromosome 10 (PTEN) phosphorylation in experimental subarachnoid hemorrhage.
Treatment with sodium orthovanadate reduces blood-brain barrier disruption via phosphatase and tensin homolog deleted on chromosome 10 (PTEN) phosphorylation in experimental subarachnoid hemorrhage.
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DOI：
10.1002/jnr.22801
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发表时间：
2012-03
影响因子：
4.2
通讯作者：
Zhang, John H.
中科院分区：
文献类型：
--
作者：
Hasegawa, Yu;Suzuki, Hidenori;Altay, Orhan;Chen, Hank;Zhang, John H.
关键词：
Attenuation of blood-brain barrier (BBB) disruption is one of the therapeutic candidates for treatment of subarachnoid hemorrhage (SAH). In this study, the protective effect of sodium orthovanadate (SOV) on BBB disruption was investigated in SAH using the endovascular perforation model. Fifty-five rats were randomly assigned to sham-operated, SAH treated with saline (as a vehicle) or 10mg/kg SOV groups, and evaluated for neurofunction and Evans blue dye extravasation. The phosphorylation of phosphatase and tensin homolog deleted on chromosome 10 (PTEN) and mitogen-activated protein kinase (MAPK), and the expression of matrix metalloproteinase-9 (MMP-9), occludin, and collagen-IV were examined by Western blot analyses. Cell death on endothelial cells were revealed by immunofluorescence and terminal deoxynucleotidyl transferase-mediated uridine 5′-triphosphate-biotin nick end-labeling (TUNEL) staining. SOV significantly improved neurofunction and reduced Evans blue dye extravasation in brains after SAH. SOV phosphorylated PTEN, decreased phospho-JNK and MMP-9, and preserved occludin expression. SOV also attenuated SAH-induced capillary endothelial cell death. The current study showed that SOV was protective against BBB disruption after SAH possibly via PTEN phosphorylation.
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影响因子：
5.1
作者：
Sehba, Fatima A.;Pluta, Ryszard M.;Zhang, John H.
通讯作者：
Zhang, John H.
影响因子：
8.3
作者：
Park, S;Yamaguchi, M;Zhang, JH
通讯作者：
Zhang, JH
影响因子：
4.2
作者：
Yatsushige, Hiroshi;Ostrowski, Robert P.;Zhang, John H.
通讯作者：
Zhang, John H.
影响因子：
8.3
作者：
Claassen, J;Carhuapoma, JR;Mayer, SA
通讯作者：
Mayer, SA
影响因子：
4
作者：
Li, Li;Ross, Alonzo H.
通讯作者：
Ross, Alonzo H.