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논문 기본 정보

자료유형
학술저널
저자정보
Myung-Ho Kim (Korea Advanced Institute of Science and Technology) Hee-Hoon Kim (Korea Advanced Institute of Science and Technology) Jong-Min Jeong (Korea Advanced Institute of Science and Technology) Young-Ri Shim (Korea Advanced Institute of Science and Technology) Jun-Hee Lee (Korea Advanced Institute of Science and Technology) Ye Eun Kim (Korea Advanced Institute of Science and Technology) Tom Ryu (Korea Advanced Institute of Science and Technology) Keungmo Yang (Korea Advanced Institute of Science and Technology) Kyu-Rae Kim (Korea Advanced Institute of Science and Technology) Byeong-Min Jeon (Korea Advanced Institute of Science and Technology) Sun Chang Kim (Korea Advanced Institute of Science and Technology) Jae-Kwang Jung (Kyungpook National University) Jae-Kap Choi (Kyungpook National University) Young-Sun Lee (Korea University College of Medicine) Jin-Seok Byun (Kyungpook National University) Won-Il Jeong (Korea Advanced Institute of Science and Technology)
저널정보
고려인삼학회 Journal of Ginseng Research Journal of Ginseng Research Vol.44 No.6
발행연도
2020.11
수록면
815 - 822 (8page)

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초록· 키워드

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Background: Recently, beneficial roles of ginsenoside F2 (GF2), a minor constituent of Panax ginseng, have been demonstrated in diverse inflammatory diseases. However, its roles in alcoholic liver inflammation and injury have not been clearly understood. Here, we investigated the underlying mechanism by which GF2 ameliorated alcoholic liver injury.
Methods: To induce alcoholic liver injury, C57BL/6J wild type (WT) or interleukin (IL)-10 knockout (KO) mice were orally administered with ethanol (3 g/kg) or ethanol-containing GF2 (50 mg/kg) for 2 wk. Liver injury and infiltration of macrophages and neutrophils were evaluated by serum biochemistry and immunohistochemistry, respectively. The changes of hepatic immune cells were assessed by flow cytometry and polymerase chain reaction analysis. In vitro differentiation of naïve T cells was performed.
Results: GF2 treatment significantly attenuated alcoholic liver injury, in which infiltrations of inflammatory macrophages and neutrophils were decreased. Moreover, the frequencies of Foxp3+ regulatory T cells (Tregs) increased but IL-17eproducing T (Th17) cells decreased in GF2-treated mice compared to controls. Furthermore, the mRNA expression of IL-10 and Foxp3 was significantly increased, whereas IL- 17 mRNA expression was suppressed in GF2-treated mice. However, these beneficial roles of GF2 were not observed in GF2-treated IL-10 KO mice, suggesting a critical role of IL-10. Similarly, GF2 treatment suppressed differentiation of naïve T cells into Th17 cells by inhibiting RORγt expression and stimulating Foxp3 expression.
Conclusion: The present study suggests that GF2 treatment attenuates alcoholic liver injury by increasing IL-10 expression and Tregs and decreasing IL-17 expression and Th17 cells.

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ABSTRACT
1. Introduction
2. Materials and methods
3. Results
4. Discussion
References

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