97%) on the interleukin (IL)-6, macrophage inflammatory protein (MIP)-2 and nitric oxide (NO) in LPS-induced shock'/> Inhibitory mechanisms of highly purified vitamin B-2 on the productions of proinflammatory cytokine and NO in endotoxin-induced shock in mice
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Inhibitory mechanisms of highly purified vitamin B-2 on the productions of proinflammatory cytokine and NO in endotoxin-induced shock in mice

机译:高纯维生素B-2对内毒素诱导的休克小鼠促炎细胞因子和NO产生的抑制机制

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摘要

Inhibitory effects of highly purified vitamin B-2 (riboflavin-5'-sodium phosphate, > 97%) on the interleukin (IL)-6, macrophage inflammatory protein (MIP)-2 and nitric oxide (NO) in LPS-induced shock mice were evaluated. Vitamin B-2 at 20 mg/kg (protective effect on mice mortality induced by LPS), intravenously administered 6 h after LPS injection, significantly decreased the plasma elevated levels of IL-6 and MIP-2 at 9 and 12 h. In addition, vitamin 132 lowered the tissue concentration and the mRNA expression of IL-6 in lung and those of MIP-2 in liver at 9 h. Vitamin B-2 also reduced concentration of MIP-2 concentration in lung, and inhibited mRNA expression in kidney, respectively. Vitamin B-2 decreased the plasma elevated NO levels in accordance with a reduction in expression of inducible NO synthase (iNOS) both at 21 and 24 h. Accordingly, the reduction in elevated plasma cytokine levels and NO based on the inhibitory effect on local cytokine mRNA expression and iNOS would be responsible for the anti-septic effect of vitamin B-2. (c) 2005 Elsevier Inc. All rights reserved.
机译:高纯度维生素B-2(核黄素5'-磷酸钠,> 97%)对LPS诱发的休克中白介素(IL)-6,巨噬细胞炎性蛋白(MIP)-2和一氧化氮(NO)的抑制作用评估小鼠。 LPS注射后6 h静脉给药的20 mg / kg维生素B-2(对LPS诱导的小鼠死亡率具有保护作用)在9和12 h时可显着降低血浆中IL-6和MIP-2的升高水平。此外,维生素132在9 h降低了肺组织和MIP-2的组织浓度和mRNA表达,并降低了MIP-2的表达。维生素B-2还可降低肺中MIP-2的浓度,并抑制肾脏中的mRNA表达。维生素B-2降低了血浆中升高的一氧化氮水平,这与21和24小时时诱导型一氧化氮合酶(iNOS)的表达降低有关。因此,基于对局部细胞因子mRNA表达和iNOS的抑制作用,降低的血浆细胞因子水平和NO的降低将是维生素B-2的防腐作用的原因。 (c)2005 Elsevier Inc.保留所有权利。

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