冰片联合灯盏花素对缺氧复氧损伤血脑屏障通透性影响.docVIP

冰片联合灯盏花素对缺氧复氧损伤血脑屏障通透性影响.doc

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冰片联合灯盏花素对缺氧复氧损伤血脑屏障通透性影响

冰片联合灯盏花素对缺氧复氧损伤血脑屏障通透性影响   摘要:目的 观察冰片联合灯盏花素对缺氧/复氧下血脑屏障(BBB)通透性的影响,探讨其保护BBB的作用机制。方法 培养原代大鼠脑微血管内皮细胞(BMEC),在缺氧培养箱中缺氧2 h,再复氧24 h,建立单层BMEC体外BBB模型。实验分为正常对照组、模型组、冰片组、灯盏花素组、冰片+灯盏花素组,各给药组给予相应药物干预,检测各组跨内皮细胞电阻(TEER)值和辣根过氧化物酶(HRP)的通透性,ELISA、Western blot检测BMEC中紧密连接蛋白ZO-1及Claudin-5蛋白表达。结果 缺氧/复氧损伤导致TEER值降低,HRP通透率增加,ZO-1及Claudin-5蛋白表达降低;冰片联合灯盏花素可明显改善上述损伤。结论 冰片联合灯盏花素对缺氧/复氧下BBB的损伤具有保护作用,其机制可能与上调ZO-1、Claudin-5蛋白表达有关。   关键词:冰片;灯盏花素;血脑屏障;大鼠   DOI:10.3969/j.issn.1005-5304.2016.02.021   中图分类号:R285.5 文献标识码:A 文章编号:1005-5304(2016)02-0076-03   Effects of Borneolum Syntheticum Combined with Breviscapine on Blood-brain Barrier Permeability Induced by Hypoxia/Reoxygenation Injury XU Lu1, ZHANG Tai-jun2 (1. Key Lab of Biochemical and Molecular Pharmacology, Chongqing Medical University, Chongqing 400016, China; 2. Chongqing City Hospital of Traditional Chinese Medicine, Chongqing 400021, China)   Abstract: Objective To observe effects of Borneolum Syntheticum combined with breviscapine on blood-brain barrier (BBB) permeability induced by hypoxia/reoxygenation injury. Methods The BBB model in vitro was established by primarily culturing brain microvascular endothelial cells (BMEC), hypoxia 2 h and reoxygenation 24 h. The experiment was divided into normal control group, model group, Borneolum Syntheticum group, breviscapine group, and Borneolum Syntheticum-breviscapine group. All treatment groups were given relevant medicine. TEER and HRP were detected; ELISA and Western blot was used to detect the expressions of ZO-1 and Claudin-5 in BMEC. Results Hypoxia/reoxygenation induced injury decreased TEER, increased permeability rate of HRP, and decreased the expressions of ZO-1 and Claudin-5; while Borneolum Syntheticum combined with breviscapine could improve damage caused by hypoxia/reoxygenation. Conclusion Borneolum Syntheticum combined with breviscapine shows obvious protective effect on BBB permeability induced by hypoxia/reoxygenation, and the mechanism is involved in the regulation of ZO

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