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硫化氢减轻大鼠蛛网膜下腔出血后早期脑损伤中的脑水肿:基质金属蛋白酶-9诱导的血脑屏障破坏和水通道蛋白4表达可能与之相关。

Hydrogen sulfide attenuates brain edema in early brain injury after subarachnoid hemorrhage in rats: Possible involvement of MMP-9 induced blood-brain barrier disruption and AQP4 expression.

作者信息

Cao Shenglong, Zhu Ping, Yu Xiaobo, Chen Jingyin, Li Jianru, Yan Feng, Wang Lin, Yu Jun, Chen Gao

机构信息

Department of Neurosurgery, The Second Affiliated Hospital of Zhejiang University, School of Medicine, Hangzhou, China.

Department of Neurosurgery, The Second Affiliated Hospital of Zhejiang University, School of Medicine, Hangzhou, China.

出版信息

Neurosci Lett. 2016 May 16;621:88-97. doi: 10.1016/j.neulet.2016.04.018. Epub 2016 Apr 11.

Abstract

AIMS

This study investigated the effect of H2S on brain edema formation and the possible underlying mechanisms in early brain injury (EBI) of SAH using the endovascular perforation model.

METHODS

96 male rats were randomly divided into four groups: sham group, SAH+vehicle group, SAH+low-dosage NaHS group, and SAH+high-dosage NaHS group. Brain samples were used for brain water content and blood-brain barrier (BBB) leakage measurement, gelatin zymography, Western blot and immunohistochemistry.

RESULTS

H2S markedly attenuated brain edema formation and apoptotic cell death, improved neurological dysfunction in the acute stage of SAH. The possible mechanisms of H2S's effect on brain edema formation were through preventing BBB disruption and reducing APQ4 expression on astrocytes. In detail, H2S prevented BBB disruption by inhibiting MMP-9 induced tight junction proteins (TJPs) degradation. H2S down-regulated AQP4 expression on astrocytes by suppressing glial cell activation and pro-inflammatory cytokines secretion.

CONCLUSION

Taken together, this study showed that H2S attenuated brain edema formation partially by inhibiting the degradation of TJPs via reducing MMP-9 expression/activity and suppressing AQP4 expression via alleviating glia activation and pro-inflammatory cytokines secretion.

摘要

目的

本研究采用血管内穿刺模型,探讨硫化氢(H2S)对蛛网膜下腔出血(SAH)早期脑损伤(EBI)脑水肿形成的影响及其潜在机制。

方法

将96只雄性大鼠随机分为四组:假手术组、SAH+溶剂组、SAH+低剂量硫氢化钠(NaHS)组和SAH+高剂量NaHS组。取脑样本用于测量脑含水量和血脑屏障(BBB)渗漏、明胶酶谱分析、蛋白质免疫印迹法和免疫组织化学。

结果

H2S显著减轻SAH急性期的脑水肿形成和凋亡性细胞死亡,改善神经功能障碍。H2S影响脑水肿形成的可能机制是通过防止BBB破坏和降低星形胶质细胞上水通道蛋白4(AQP4)的表达。具体而言,H2S通过抑制基质金属蛋白酶9(MMP-9)诱导的紧密连接蛋白(TJPs)降解来防止BBB破坏。H2S通过抑制胶质细胞活化和促炎细胞因子分泌来下调星形胶质细胞上AQP4的表达。

结论

综上所述,本研究表明H2S部分通过降低MMP-9表达/活性抑制TJPs降解以及通过减轻胶质细胞活化和促炎细胞因子分泌抑制AQP4表达来减轻脑水肿形成。

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