Ahn Huijeong, Han Byung-Cheol, Kim Jeongeun, Kang Seung Goo, Kim Pyeung-Hyeun, Jang Kyoung Hwa, So Seung Ho, Lee Seung-Ho, Lee Geun-Shik
College of Veterinary Medicine and Institute of Veterinary Science, Kangwon National University, Chuncheon, Republic of Korea.
Korea Ginseng Research Institute, Korea Ginseng Corporation, Daejeon, Republic of Korea.
J Ginseng Res. 2019 Apr;43(2):291-299. doi: 10.1016/j.jgr.2018.03.003. Epub 2018 Apr 4.
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.
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.
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.
NS administration directly inhibits TLR4 expression in inflammatory cells such as macrophages, thereby reducing secretion of cytokines during peritonitis.
高丽参提取物(RGE)的人参皂苷及其皂苷成分可抑制炎性小体介导的细胞因子分泌,而RGE的非皂苷部分(NS)则相反地刺激细胞因子分泌。尽管将NS直接暴露于小鼠巨噬细胞可诱导细胞因子产生,但尚未在动物模型的炎性小体相关疾病中研究NS的口服给药情况。
给小鼠喂食RGE或NS 7天,然后诱发腹膜炎。测量腹膜细胞因子,并收集腹膜渗出细胞(PEC)以检测一组Toll样受体(TLR)的表达水平以及对NS摄入的细胞因子反应。此外,评估了肠道细菌在喂食NS的小鼠中的作用。进一步证实了在骨髓来源的巨噬细胞(BMDM)中预先暴露于NS对细胞因子产生的影响。
摄入NS可减轻腹膜炎导致的腹膜细胞因子分泌。此外,与喂食对照饮食的小鼠的PEC相比,从喂食NS的小鼠中分离出的PEC呈现出较低的TLR转录水平。用NS处理的BMDM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配体产生的细胞因子较少。
给予NS可直接抑制巨噬细胞等炎性细胞中TLR4的表达,从而减少腹膜炎期间细胞因子的分泌。