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首页> 外文期刊>Molecular medicine reports >Epoxyeicosatrienoic acid ameliorates cerebral ischemia-reperfusion injury by inhibiting inflammatory factors and pannexin-1
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Epoxyeicosatrienoic acid ameliorates cerebral ischemia-reperfusion injury by inhibiting inflammatory factors and pannexin-1

机译:环氧喹喔啉酸通过抑制炎症因素和Pannexin-1来改善脑缺血再灌注损伤

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摘要

Epoxyeicosatrienoic acid (EET) has wide applications due to the unique biological effects of antihyper-lipidemia, inhibition of platelet aggregation, anti-inflammation, anti-cancer, anti-lipid oxidation and the promotion of brain tissue development. The present study investigated whether EET ameliorates cerebral ischemia-reperfusion injury (CIRI) by inhibiting inflammatory factors and pannexin. Specific pathogen-free 7-week-old male Sprague-Dawley rats were randomly divided into three groups: Sham, CIRI and EET. Neurological deficit scores, cerebral infarct volume and cerebral edema were assessed in CIRI rats. Enzyme-linked immunosorbent assays were performed to detect tumor necrosis factor-a, interleukin-6, nuclear factor-kappa B and inducible nitric oxide synthase (iNOS) levels, and western blot analysis was performed also used to assess cleaved caspase-3, phospholipase A2 (PLA2), cyclooxygenase-2 and prostaglandin E2 (PGE2) protein expression levels. EET ameliorated cerebral injury and CIRI-induced cleaved caspase-3 protein expression levels in rats. EET additionally suppressed CIRI-induced inflammation reactions and iNOS protein expression in rats. Furthermore, the protein expression levels of PLA2, PGE2 and pannexin-1 in CIRI rats were inhibited by treatment with EET. These results indicated that EET reduces CIRI by inhibiting inflammation and levels of cleaved caspase-3, PLA2, PGE2 and pannexin-1.
机译:环氧基辛酸甲酸(EET)具有广泛的应用,由于抗滑坡 - 脂质血症的独特生物学效应,抑制血小板聚集,抗炎,抗癌,抗脂氧化和促进脑组织发育。本研究研究了EET是否通过抑制炎症因子和Pangexin来改善脑缺血再灌注损伤(CIRI)。特定的病原体7周龄雄性Sprague-Dawley大鼠随机分为三组:假,Ciri和Eet。在CiRi大鼠中评估神经缺陷分数,脑梗塞体积和脑水肿。进行酶联免疫吸附测定以检测肿瘤坏死因子-A,白细胞介素-6,核因子-Kappa B和诱导的一氧化氮合酶(InOS)水平,并进行Western印迹分析,也用于评估切割的Caspase-3,磷脂酶A2(PLA2),环加氧酶-2和前列腺素E2(PGE2)蛋白表达水平。 EET改善脑损伤和CIRI诱导的大鼠切割的裂解胱天蛋白酶-3蛋白表达水平。 EET另外抑制了大鼠中的CIRI诱导的炎症反应和INOS蛋白表达。此外,通过用EET治疗抑制CIRI大鼠中PLA2,PGE2和PANNEXIN-1的蛋白质表达水平。这些结果表明,EET通过抑制切割的Caspase-3,PLA2,PGE2和Pannexin-1的炎​​症和水平来减少CIRI。

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