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本文引用的文献

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Development of a stretch-induced neurotrauma model for medium-throughput screening in vitro: identification of rifampicin as a neuroprotectant.拉伸诱导的神经创伤模型的建立用于体外高通量筛选:利福平作为神经保护剂的鉴定。
Br J Pharmacol. 2018 Jan;175(2):284-300. doi: 10.1111/bph.13642. Epub 2016 Nov 15.
2
Lipid peroxidation and tyrosine nitration in traumatic brain injury: Insights into secondary injury from redox proteomics.创伤性脑损伤中的脂质过氧化和酪氨酸硝化:氧化还原蛋白质组学对继发性损伤的见解
Proteomics Clin Appl. 2016 Dec;10(12):1191-1204. doi: 10.1002/prca.201600003. Epub 2016 Oct 14.
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Glibenclamide Attenuates Blood-Brain Barrier Disruption in Adult Mice after Traumatic Brain Injury.格列本脲减轻成年小鼠创伤性脑损伤后的血脑屏障破坏
J Neurotrauma. 2017 Feb 15;34(4):925-933. doi: 10.1089/neu.2016.4491. Epub 2016 Jul 8.
4
ROS and ROS-Mediated Cellular Signaling.活性氧(ROS)与 ROS 介导的细胞信号转导。
Oxid Med Cell Longev. 2016;2016:4350965. doi: 10.1155/2016/4350965. Epub 2016 Feb 22.
5
Hydrogen-rich water attenuates brain damage and inflammation after traumatic brain injury in rats.富氢水可减轻大鼠创伤性脑损伤后的脑损伤和炎症反应。
Brain Res. 2016 Apr 15;1637:1-13. doi: 10.1016/j.brainres.2016.01.029. Epub 2016 Jan 26.
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Establishment and Dysfunction of the Blood-Brain Barrier.血脑屏障的建立和功能障碍。
Cell. 2015 Nov 19;163(5):1064-1078. doi: 10.1016/j.cell.2015.10.067.
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SIRT2 inhibition exacerbates neuroinflammation and blood-brain barrier disruption in experimental traumatic brain injury by enhancing NF-κB p65 acetylation and activation.沉默调节蛋白2(SIRT2)抑制通过增强核因子κB(NF-κB)p65的乙酰化和激活,加重实验性创伤性脑损伤中的神经炎症和血脑屏障破坏。
J Neurochem. 2016 Feb;136(3):581-93. doi: 10.1111/jnc.13423. Epub 2015 Dec 7.
8
Stretch and/or oxygen glucose deprivation (OGD) in an in vitro traumatic brain injury (TBI) model induces calcium alteration and inflammatory cascade.在体外创伤性脑损伤(TBI)模型中,拉伸和/或氧葡萄糖剥夺(OGD)会引发钙变化和炎症级联反应。
Front Cell Neurosci. 2015 Aug 21;9:323. doi: 10.3389/fncel.2015.00323. eCollection 2015.
9
Protective properties of sesamin against fluoride-induced oxidative stress and apoptosis in kidney of carp (Cyprinus carpio) via JNK signaling pathway.芝麻素通过JNK信号通路对鲤鱼(Cyprinus carpio)肾脏中氟诱导的氧化应激和细胞凋亡的保护作用。
Aquat Toxicol. 2015 Oct;167:180-90. doi: 10.1016/j.aquatox.2015.08.004. Epub 2015 Aug 18.
10
Melatonin alleviates brain injury in mice subjected to cecal ligation and puncture via attenuating inflammation, apoptosis, and oxidative stress: the role of SIRT1 signaling.褪黑素通过减轻炎症、细胞凋亡和氧化应激减轻盲肠结扎穿孔小鼠的脑损伤:SIRT1 信号通路的作用。
J Pineal Res. 2015 Sep;59(2):230-9. doi: 10.1111/jpi.12254. Epub 2015 Jun 24.

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.

DOI:10.1038/aps.2017.103
PMID:28770828
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5672062/
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。