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首页> 外文期刊>Chinese Medical Journal >Green tea polyphenol epigallocatechin-3-gallate inhibits the expression of nitric oxide synthase and generation of nitric oxide induced by ultraviolet B in HaCaT cells
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Green tea polyphenol epigallocatechin-3-gallate inhibits the expression of nitric oxide synthase and generation of nitric oxide induced by ultraviolet B in HaCaT cells

机译:绿茶多酚表没食子儿茶素-3-没食子酸酯抑制HaCaT细胞中一氧化氮合酶的表达和紫外线B诱导的一氧化氮的产生

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摘要

Background Nitic oxide (NO) has been implicated in the pathogenesis of various inflammatory diseases, including sunburn and pigmentation induced by ultraviolet irradiation. Epigallocatechin-3-gallate (EGCG) is the major effective component in green tea and can protect skin from ultraviolet-induced damage. The purpose of this study was to investigate the protective mechanisms of EGCG on inducible nitric oxide synthase (iNOS) expression and NO generation by ultraviolet B (UVB) irradiation in HaCaT cells. Methods HaCaT cells were irradiated with UVB 30 mJ/cm~2 and pretreated with EGCG at varying concentrations. The iNOS mRNA was detected by reverse transcriptase polymerase chain reaction (RT-PCR) and NO production was quantified by spectrophotometric method. The expression of NF-κB P65 was measured by immunofluorescence cytochemistry staining. Results The expression of iNOS mRNA and generation of NO in HaCaT cells were increased by UVB irradiation. EGCG down regulated the UVB-induced iNOS mRNA synthesis and NO generation in a dose dependent manner. The UVB-induced activation and translocation of NF-κB were also down regulated by EGCG treatment in HaCaT cells (P < 0.01). Conclusions Green tea derived-EGCG can inhibit and down regulate the UVB-induced activation and translocation of NF-κB, expression of iNOS mRNA and generation of NO respectively, indicating EGCG may play a protective role from UVB-induced skin damage.
机译:背景技术一氧化氮(NO)与多种炎性疾病的发病机制有关,包括晒伤和紫外线照射引起的色素沉着。 Epigallocatechin-3-gallate(EGCG)是绿茶中的主要有效成分,可以保护皮肤免受紫外线引起的伤害。这项研究的目的是研究EGCG对HaCaT细胞中诱导型一氧化氮合酶(iNOS)表达和紫外线B(UVB)照射产生NO的保护机制。方法用30 mJ / cm〜2的UVB照射HaCaT细胞,并用不同浓度的EGCG预处理。通过逆转录酶聚合酶链反应(RT-PCR)检测iNOS mRNA,并通过分光光度法定量NO的产生。通过免疫荧光细胞化学染色检测NF-κBP65的表达。结果UVB诱导HaCaT细胞iNOS mRNA表达和NO生成增加。 EGCG以剂量依赖性方式下调UVB诱导的iNOS mRNA合成和NO生成。 EGCG处理后,HaCaT细胞中UVB诱导的NF-κB活化和转位也被下调(P <0.01)。结论绿茶来源的EGCG可以抑制和下调UVB诱导的NF-κB的活化和转运,iNOS mRNA的表达和NO的生成,表明EGCG可能对UVB诱导的皮肤损伤具有保护作用。

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