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Nonsaponin fraction of Korean Red Ginseng attenuates cytokine production via inhibition of TLR4 expression

机译:高丽红参中的非皂苷成分通过抑制TLR4表达来减弱细胞因子的产生

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Background Ginsenosides of Korean Red Ginseng extracts (RGE) and its saponin components suppress secretion of inflammasome-mediating cytokines, whereas the nonsaponin fraction (NS) of RGE oppositely stimulates cytokine secretion. Although direct exposure of NS to macrophages in mice induces cytokine production, oral administration of NS has not been studied in inflammasome-related disease in animal models. Methods Mice were fed RGE or NS for 7 days and then developed peritonitis. Peritoneal cytokines were measured, and peritoneal exudate cells (PECs) were collected to assay expression levels of a set of toll-like receptors (TLRs) and cytokines in response to NS ingestion. In addition, the role of intestinal bacteria in NS-fed mice was assessed. The effect of preexposure to NS in bone marrow–derived macrophages (BMDMs) on cytokine production was further confirmed. Results NS ingestion attenuated secretion of peritoneal cytokines resulting from peritonitis. In addition, the isolated PECs from NS-fed mice presented lower TLR transcription levels than PECs from control diet–fed mice. BMDMs treated with NS showed downregulation of TLR4 mRNA and protein expression, which was mediated by the TLR4-MyD88-NFκB signal pathway. BMDMs pretreated with NS produced less cytokines in response to TLR4 ligands. Conclusion NS administration directly inhibits TLR4 expression in inflammatory cells such as macrophages, thereby reducing secretion of cytokines during peritonitis.
机译:韩国红参提取物(RGE)的人参皂苷及其皂苷成分抑制介导炎性体的细胞因子的分泌,而RGE的非皂苷组分(NS)相反地刺激细胞因子的分泌。尽管将NS直接暴露于小鼠的巨噬细胞中会诱导细胞因子的产生,但尚未在动物模型中与炎症小体相关疾病中口服NS的研究。方法给小鼠喂食RGE或NS 7天,然后发展为腹膜炎。测量腹膜细胞因子,并收集腹膜渗出液细胞(PEC)以测定一组响应NS摄入的toll样受体(TLRs)和细胞因子的表达水平。另外,评估了肠道细菌在NS喂养的小鼠中的作用。骨髓源性巨噬细胞(BMDMs)中NS暴露前暴露对细胞因子产生的影响得到进一步证实。结果NS摄入减少了腹膜炎引起的腹膜细胞因子的分泌。此外,从NS喂养的小鼠中分离出的PEC的TLR转录水平低于对照饮食喂养的小鼠中的PEC。 NS处理的BMDMs显示TLR4 mRNA和蛋白表达下调,这是由TLR4-MyD88-NFκB信号通路介导的。用NS预处理的BMDM对TLR4配体的反应产生的细胞因子较少。结论NS给药可直接抑制TLR4在炎性细胞(如巨噬细胞)中的表达,从而减少腹膜炎期间细胞因子的分泌。

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