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18β-甘草次酸诱导巨噬细胞中诱导型一氧化氮合酶的表达

Induction of inducible nitric oxide synthase expression by 18beta-glycyrrhetinic acid in macrophages.

作者信息

Jeong Hye Gwang, Kim Ji Young

机构信息

Department of Pharmacy, College of Pharmacy, Chosun University, 375 Seosuk-dong, 501-759, Kwangju, South Korea.

出版信息

FEBS Lett. 2002 Feb 27;513(2-3):208-12. doi: 10.1016/s0014-5793(02)02311-6.

Abstract

Glycyrrhizin (GL), a triterpenoid saponin fraction of licorice, is reported to have anti-viral and anti-tumor activities and is metabolized to 18beta-glycyrrhetinic acid (GA) in the intestine by intestinal bacteria. However, the mechanism underlying its effects is poorly understood. To further elucidate the mechanism of GA, the aglycone of GL, we investigated the effects of GA on the release of nitric oxide (NO) and at the level of inducible NO synthase (iNOS) gene expression in mouse macrophages. We found that GA elicited a dose-dependent increase in NO production and in the level of iNOS mRNA. Since iNOS transcription has been shown to be under the control of the transcription factor nuclear factor kappaB (NF-kappaB), the effects of GA on NF-kappaB activation were examined. Transient expression assays with NF-kappaB binding sites linked to the luciferase gene revealed that the increased level of iNOS mRNA, induced by GA, was mediated by the NF-kappaB transcription factor complex. By using DNA fragments containing the NF-kappaB binding sequence, GA was shown to activate the protein/DNA binding of NF-kappaB to its cognate site, as measured by electrophoretic mobility shift assay. These results demonstrate that GA stimulates NO production and is able to up-regulate iNOS expression through NF-kappaB transactivation in macrophages.

摘要

甘草甜素(GL)是甘草中的一种三萜皂苷成分,据报道具有抗病毒和抗肿瘤活性,在肠道中会被肠道细菌代谢为18β-甘草次酸(GA)。然而,其作用的潜在机制尚不清楚。为了进一步阐明GL的苷元GA的作用机制,我们研究了GA对小鼠巨噬细胞中一氧化氮(NO)释放以及诱导型一氧化氮合酶(iNOS)基因表达水平的影响。我们发现GA引起了NO产生以及iNOS mRNA水平的剂量依赖性增加。由于iNOS转录已被证明受转录因子核因子κB(NF-κB)的控制,因此研究了GA对NF-κB激活的影响。用与荧光素酶基因相连的NF-κB结合位点进行瞬时表达分析表明,GA诱导的iNOS mRNA水平升高是由NF-κB转录因子复合物介导的。通过使用含有NF-κB结合序列的DNA片段,电泳迁移率变动分析表明GA能够激活NF-κB与其同源位点的蛋白质/DNA结合。这些结果表明,GA刺激NO产生,并能够通过巨噬细胞中的NF-κB反式激活上调iNOS表达。

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