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芝麻素可减轻实验性创伤性脑损伤小鼠的血脑屏障破坏。

Sesamin alleviates blood-brain barrier disruption in mice with experimental traumatic brain injury.

作者信息

Liu Ying-Liang, Xu Zhi-Ming, Yang Guo-Yuan, Yang Dian-Xu, Ding Jun, Chen Hao, Yuan Fang, Tian Heng-Li

机构信息

Department of Neurosurgery, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200233, China.

Med-X Research Institute and School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai 200233, China.

出版信息

Acta Pharmacol Sin. 2017 Nov;38(11):1445-1455. doi: 10.1038/aps.2017.103. Epub 2017 Aug 3.

Abstract

Sesamin, a major lignan of sesame oil, was reported to have neuroprotective effects in several brain injury models. However, its protective action in maintaining blood-brain barrier (BBB) integrity has not been studied. In this study we investigated the effects of sesamin on the BBB in a mouse model of traumatic brain injury (TBI) and explored the underlying mechanisms. Adult male C57BL/6 mice were subjected to a controlled cortical impact (CCI) injury and then received sesamin (30 mg·kg·d, ip). The mice were euthanized on the 1 and 3 days after CCI injury and samples were collected for analysis. Sesamin treatment significantly attenuated CCI-induced brain edema on the 1 and 3 days after the injury, evidenced by the decreases in water content, tissue hemoglobin levels, Evans blue extravasation and AQP4 expression levels in the ipsilateral cortical tissue compared with the vehicle-treated group. Furthermore, sesamin treatment significantly alleviated CCI-induced loss of the tight junction proteins ZO-1 and occludin in the brain tissues. The neuroprotective mechanisms of sesamin were further explored in cultured mouse brain microvascular bEnd.3 cells subjected to biaxial stretch injury (SI). Pretreatment with sesamin (50 μmol/L) significantly alleviated SI-induced loss of ZO-1 in bEnd.3 cells. Furthermore, we revealed that pretreatment with sesamin significantly attenuated SI-induced oxidative stress and early-stage apoptosis in bEnd.3 cells by decreasing the activation of ERK, p-38 and caspase-3. In conclusion, sesamin alleviates BBB disruption at least partly through its anti-oxidative and anti-apoptotic effects on endothelial cells in CCI injury. These findings suggest that sesamin may be a promising potential therapeutic intervention for preventing disruption of the BBB after TBI.

摘要

芝麻素是芝麻油中的一种主要木脂素,据报道在多种脑损伤模型中具有神经保护作用。然而,其在维持血脑屏障(BBB)完整性方面的保护作用尚未得到研究。在本研究中,我们调查了芝麻素对创伤性脑损伤(TBI)小鼠模型中血脑屏障的影响,并探讨了其潜在机制。成年雄性C57BL/6小鼠接受控制性皮质撞击(CCI)损伤,然后接受芝麻素(30 mg·kg·d,腹腔注射)。在CCI损伤后的第1天和第3天对小鼠实施安乐死,并收集样本进行分析。与载体处理组相比,芝麻素处理在损伤后的第1天和第3天显著减轻了CCI诱导的脑水肿,同侧皮质组织中的含水量、组织血红蛋白水平、伊文思蓝外渗和水通道蛋白4表达水平降低证明了这一点。此外,芝麻素处理显著减轻了CCI诱导的脑组织中紧密连接蛋白ZO-1和闭合蛋白的丢失。在遭受双轴拉伸损伤(SI)的培养小鼠脑微血管bEnd.3细胞中进一步探索了芝麻素的神经保护机制。用芝麻素(50 μmol/L)预处理显著减轻了SI诱导的bEnd.3细胞中ZO-1的丢失。此外,我们发现用芝麻素预处理通过降低ERK、p-38和半胱天冬酶-3的激活,显著减轻了SI诱导的bEnd.3细胞中的氧化应激和早期凋亡。总之,芝麻素至少部分通过其对CCI损伤中内皮细胞的抗氧化和抗凋亡作用减轻血脑屏障破坏。这些发现表明,芝麻素可能是预防TBI后血脑屏障破坏的一种有前景的潜在治疗干预措施。

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