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首页> 外文期刊>Critical care : >Hypertonic saline reduces lipopolysaccharide-induced mouse brain edema through inhibiting aquaporin 4 expression
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Hypertonic saline reduces lipopolysaccharide-induced mouse brain edema through inhibiting aquaporin 4 expression

机译:高渗盐水通过抑制水通道蛋白4的表达减少脂多糖诱导的小鼠脑水肿

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IntroductionThree percent sodium chloride (NaCl) treatment has been shown to reduce brain edema and inhibited brain aquaporin 4 (AQP4) expression in bacterial meningitis induced by Escherichia coli. Lipopolysaccharide (LPS) is the main pathogenic component of E. coli. We aimed to explore the effect of 3% NaCl in mouse brain edema induced by LPS, as well as to elucidate the potential mechanisms of action.MethodsThree percent NaCl was used to treat cerebral edema induced by LPS in mice in vivo. Brain water content, IL-1β, TNFα, immunoglobulin G (IgG), AQP4 mRNA and protein were measured in brain tissues. IL-1β, 3% NaCl and calphostin C (a specific inhibitor of protein kinase C) were used to treat the primary astrocytes in vitro. AQP4 mRNA and protein were measured in astrocytes. Differences in various groups were determined by one-way analysis of variance.ResultsThree percent NaCl attenuated the increase of brain water content, IL-1β, TNFα, IgG, AQP4 mRNA and protein in brain tissues induced by LPS. Three percent NaCl inhibited the increase of AQP4 mRNA and protein in astrocytes induced by IL-1β in vitro. Calphostin C blocked the decrease of AQP4 mRNA and protein in astrocytes induced by 3% NaCl in vitro.ConclusionsOsmotherapy with 3% NaCl ameliorated LPS-induced cerebral edema in vivo. In addition to its osmotic force, 3% NaCl exerted anti-edema effects possibly through down-regulating the expression of proinflammatory cytokines (IL-1β and TNFα) and inhibiting the expression of AQP4 induced by proinflammatory cytokines. Three percent NaCl attenuated the expression of AQP4 through activation of protein kinase C in astrocytes.
机译:简介已显示百分之三的氯化钠(NaCl)处理可减少大肠杆菌引起的细菌性脑膜炎中的脑水肿并抑制脑水通道蛋白4(AQP4)的表达。脂多糖(LPS)是大肠杆菌的主要致病成分。我们旨在探讨3%NaCl在LPS诱导的小鼠脑水肿中的作用,并阐明其潜在的作用机制。方法采用3%NaCl体内处理LPS诱导的小鼠脑水肿。测量脑组织中的脑含水量,IL-1β,TNFα,免疫球蛋白G(IgG),AQP4 mRNA和蛋白质。 IL-1β,3%NaCl和钙磷蛋白C(蛋白激酶C的特异性抑制剂)用于体外处理原代星形胶质细胞。测量星形胶质细胞中的AQP4 mRNA和蛋白。通过单向方差分析确定各组之间的差异。结果3%NaCl减弱了LPS诱导的脑组织中脑含水量,IL-1β,TNFα,IgG,AQP4 mRNA和蛋白质的增加。 3%的NaCl抑制了IL-1β诱导的星形胶质细胞AQP4 mRNA和蛋白的增加。 Calphostin C阻断了3%NaCl诱导的星形胶质细胞中AQP4 mRNA和蛋白的降低。结论3%NaCl渗透疗法可改善LPS诱导的脑水肿。除其渗透力外,3%NaCl还可能通过下调促炎细胞因子(IL-1β和TNFα)的表达并抑制促炎细胞因子诱导的AQP4的表达发挥抗水肿作用。 3%的NaCl通过激活星形胶质细胞中的蛋白激酶C减弱AQP4的表达。

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