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大豆苷元对中间普氏菌脂多糖刺激的小鼠巨噬细胞的抗炎作用及其作用机制。

Anti-inflammatory effects and the underlying mechanisms of action of daidzein in murine macrophages stimulated with Prevotella intermedia lipopolysaccharide.

机构信息

Department of Biological Science, College of Medical and Life Sciences, Silla University, Busan, Korea.

出版信息

J Periodontal Res. 2012 Apr;47(2):204-11. doi: 10.1111/j.1600-0765.2011.01422.x. Epub 2011 Oct 5.

Abstract

BACKGROUND AND OBJECTIVE

Host modulatory agents directed at inhibiting specific proinflammatory mediators could be beneficial in terms of attenuating periodontal disease progression and potentially enhancing therapeutic responses. The aim of this study was to investigate whether daidzein could modulate the production inflammatory mediators in macrophages stimulated with lipopolysaccharide (LPS) from Prevotella intermedia, a pathogen implicated in periodontal disease, and to delineate underlying mechanisms of action.

MATERIAL AND METHODS

LPS was extracted from P. intermedia ATCC 25611 cells by the standard hot phenol-water method. The amounts of nitric oxide (NO) and interleukin-6 (IL-6) secreted into the culture medium were assayed. A real-time PCR was performed to quantify inducible nitric oxide synthase (iNOS) and IL-6 mRNA expression. We used immunoblot analysis to characterize iNOS protein expression, phosphrylation of c-Jun N-terminal kinase (JNK) and p38, degradation of inhibitory κB-α (IκB-α), nuclear translocation of nuclear factor-κB (NF-κB) subunits and phosphorylation of signal transducer and activator of transcription 1 (STAT1). The DNA-binding activity of NF-κB was assessed by using ELISA-based kits.

RESULTS

Daidzein significantly inhibited the production of NO and IL-6, as well as their mRNA expression, in P. intermedia LPS-treated RAW264.7 cells. The JNK and p38 pathways were not involved in the regulation of LPS-induced NO and IL-6 release by daidzein. Daidzein inhibited the degradation of IκB-α induced by P. intermedia LPS. In addition, daidzein suppressed NF-κB transcriptional activity via regulation of the nuclear translocation and DNA-binding activity of NF-κB p50 subunit and blocked STAT1 phosphorylation.

CONCLUSION

Although additional studies are required to dissect the molecular mechanism of action, our results suggest that daidzein could be a promising agent for treating inflammatory periodontal disease. Further research in animal models of periodontitis is necessary to better evaluate the potential of daidzein as a novel therapeutic agent to treat periodontal disease.

摘要

背景与目的

靶向抑制特定促炎介质的宿主调节因子可能有益于减轻牙周病的进展,并可能增强治疗反应。本研究旨在探讨大豆苷元是否能调节脂多糖(LPS)刺激的巨噬细胞中炎症介质的产生,LPS 是一种与牙周病有关的病原体。并探讨其作用机制。

材料与方法

采用标准热酚水法从中间普氏菌 ATCC 25611 细胞中提取 LPS。测定培养基中一氧化氮(NO)和白细胞介素-6(IL-6)的分泌量。采用实时 PCR 定量检测诱导型一氧化氮合酶(iNOS)和 IL-6 mRNA 的表达。我们用免疫印迹分析来描述 iNOS 蛋白表达、c-Jun N 末端激酶(JNK)和 p38 的磷酸化、抑制性κB-α(IκB-α)的降解、核转录因子-κB(NF-κB)亚基的核转位以及信号转导和转录激活因子 1(STAT1)的磷酸化。采用 ELISA 试剂盒评估 NF-κB 的 DNA 结合活性。

结果

大豆苷元显著抑制了中间普氏菌 LPS 处理的 RAW264.7 细胞中 NO 和 IL-6 的产生及其 mRNA 的表达。JNK 和 p38 途径不参与大豆苷元调节 LPS 诱导的 NO 和 IL-6 释放。大豆苷元抑制了 LPS 诱导的 IκB-α的降解。此外,大豆苷元通过调节 NF-κB p50 亚基的核转位和 DNA 结合活性抑制 NF-κB 的转录活性,并阻断 STAT1 的磷酸化。

结论

尽管需要进一步研究来剖析其作用机制,但我们的研究结果表明,大豆苷元可能是治疗炎症性牙周病的一种有前途的药物。在牙周炎动物模型中进行进一步的研究,以更好地评估大豆苷元作为治疗牙周病的新型治疗剂的潜力是必要的。

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