首页> 外文期刊>Journal of Pharmacy and Pharmacology >The protective action of scutellarin against immunological liver injury induced by concanavalin A and its effect on pro-inflammatory cytokines in mice.
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The protective action of scutellarin against immunological liver injury induced by concanavalin A and its effect on pro-inflammatory cytokines in mice.

机译:黄cut苷对伴刀豆球蛋白A诱导的免疫性肝损伤的保护作用及其对小鼠促炎细胞因子的影响。

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摘要

Scutellarin is a natural compound from a Chinese herb. The purpose of this paper was to study the protective effect of scutellarin on concanavalin A (Con A)-induced immunological liver injury and its effect on liver nuclear factor kappaB (NF-kappaB), tumor necrosis factor alpha (TNF-alpha), interferon gamma (IFN-gamma), and inducible nitric oxide synthase (iNOS) expression in mice. Mouse liver injury was produced by injection of Con A 25 mg kg-1 via the tail vein. Scutellarin 50 or 100 mg kg-1 was peritoneally administered to mice 9 or 1 h before injection of Con A. The levels of serum alanine aminotransferase (ALT) and asparatate aminotransferase (AST), NO2-/NO3- and TNF-alpha were determined with biochemical kits, and ELISA using Quantikine Mouse TNF-alpha kit according the manufacturer's instructions. Liver lesions were examined by light microscope. The expression of TNF-alpha, IFN-gamma, iNOS and Fas mRNA in the livers was detected by RT-PCR; and the expression of c-Fos, c-Jun, iNOS and IkappaB proteins was measured by Western Blotting. As a result, pretreatment with scutellarin 100 mg kg-1 significantly decreased the serum ALT, AST, NO2-/NO3- and TNF-alpha levels, and also reduced liver lesions induced by Con A. Scutellarin 100 mg kg-1 down-regulated expression of TNF-alpha and iNOS mRNA, and c-Fos, c-Jun and iNOS protein, while scutellarin enhanced the degradation of IkappaB in the livers of mice injected with Con A. The results suggest that scutellarin has a protective action against Con A-induced liver injury in mice, and its active mechanism may be related to the inhibition of the NF-kappaB-TNF-alpha-iNOS transduction pathway.
机译:黄cut苷是来自中草药的天然化合物。本文旨在研究黄cut苷对伴刀豆球蛋白A(Con A)诱导的免疫性肝损伤的保护作用及其对肝核因子κB(NF-kappaB),肿瘤坏死因子α(TNF-alpha),干扰素的影响γ(IFN-γ)和诱导型一氧化氮合酶(iNOS)在小鼠中的表达。通过尾静脉注射Con A 25 mg kg-1产生小鼠肝损伤。在注射Con A前9或1小时腹膜内给予50或100 mg kg-1的Scutellarin。测定血清丙氨酸氨基转移酶(ALT)和天冬氨酸氨基转移酶(AST),NO2- / NO3-和TNF-α的水平使用生化试剂盒,并根据制造商的说明使用Quantikine Mouse TNF-alpha试剂盒进行ELISA。通过光学显微镜检查肝脏病变。 RT-PCR检测肝组织中TNF-α,IFN-γ,iNOS和Fas mRNA的表达。 Western blotting检测c-Fos,c-Jun,iNOS和IkappaB蛋白的表达。结果,用黄mg素100 mg kg-1预处理可显着降低血清ALT,AST,NO2- / NO3-和TNF-α水平,还减少了Con A诱导的肝损伤。黄cut素100 mg kg-1下调盾构蛋白增强了Con A注射小鼠肝脏中IkappaB的降解,TNF-α和iNOS mRNA的表达以及c-Fos,c-Jun和iNOS蛋白的表达。结果表明,盾构蛋白对Con A具有保护作用诱导的小鼠肝损伤及其激活机制可能与抑制NF-κB-TNF-α-iNOS的转导途径有关。

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