首页> 美国卫生研究院文献>Mediators of Inflammation >Red Ginseng Extract Ameliorates Autoimmune Arthritis via Regulation of STAT3 Pathway Th17/Treg Balance and Osteoclastogenesis in Mice and Human
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Red Ginseng Extract Ameliorates Autoimmune Arthritis via Regulation of STAT3 Pathway Th17/Treg Balance and Osteoclastogenesis in Mice and Human

机译:红参提取物通过调节小鼠和人类的STAT3途径Th17 / Treg平衡和破骨细胞生成来改善自身免疫性关节炎

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摘要

Rheumatoid arthritis (RA) is a systemic autoimmune disease characterized by chronic joint inflammation. Red ginseng is a steamed and dried Panax ginseng C.A. Meyer, which has been used as alternative medicine for thousands of years. This study was undertaken to investigate the effects of red ginseng extracts (RGE) on autoimmune arthritis in mice and humans and to delineate the underlying mechanism. RGE was orally administered three times a week to mice with arthritis. Oral administration of RGE markedly ameliorated clinical arthritis score and histologically assessed joint inflammation in mice with CIA. A significant reduction in STAT3 phosphorylation and a decrease in the number of Th17 cells were observed with RGE treatment. There was also a marked reduction in RANKL-induced osteoclastogenesis with treatment of RGE. The inhibitory effect of RGE on Th17 differentiation and osteoclastogenesis observed in mice was also confirmed in the subsequent experiments performed using human peripheral blood mononuclear cells. Our findings provide the first evidence that RGE can regulate Th17 and reciprocally promote Treg cells by inhibiting the phosphorylation of STAT3. Therefore, RGE can ameliorate arthritis in mice with CIA by targeting pathogenic Th17 and osteoclast differentiation, suggesting a novel therapy for treatment of RA.
机译:类风湿关节炎(RA)是一种全身性自身免疫性疾病,其特征在于慢性关节发炎。红参是蒸干的人参C.A.迈耶(Meyer)被用作替代医学已有数千年的历史了。进行这项研究以研究红参提取物(RGE)对小鼠和人类自身免疫性关节炎的影响,并阐明其潜在机制。每周对关节炎小鼠口服RGE 3次。口服RGE可以明显改善CIA小鼠的临床关节炎评分,并从组织学上评估关节炎症。用RGE处理观察到STAT3磷酸化的显着减少和Th17细胞数量的减少。用RGE治疗,RANKL诱导的破骨细胞形成也显着减少。在随后使用人外周血单核细胞进行的实验中,也证实了RGE对小鼠Th17分化和破骨细胞生成的抑制作用。我们的发现提供了第一个证据,即RGE可通过抑制STAT3的磷酸化来调节Th17并相互促进Treg细胞。因此,RGE可以通过靶向致病性Th17和破骨细胞分化来缓解CIA小鼠的关节炎,提示治疗RA的新疗法。

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