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학술저널
저자정보
Kwang-Soo Baek (Sungkyunkwan University) Yong Deog Hong (AmorePacific R&D Center) Yong Kim (Sungkyunkwan University) Nak Yoon Sung (Sungkyunkwan University) Sungjae Yang (Sungkyunkwan University) Kyoung Min Lee (Sungkyunkwan University) Joo Yong Park (Sungkyunkwan University) Jun Seong Park (AmorePacific R&D Center) Ho Sik Rho (AmorePacific R&D Center) Song Seok Shin (AmorePacific R&D Center) Jae Youl Cho (Sungkyunkwan University)
저널정보
고려인삼학회 Journal of Ginseng Research Journal of Ginseng Research Vol.39 No.2
발행연도
2015.4
수록면
155 - 161 (7page)

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이 논문의 연구 히스토리 (2)

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Background: Korean ginseng is an ethnopharmacologically valuable herbal plant with various biological properties including anticancer, antiatherosclerosis, antidiabetic, and anti-inflammatory activities. Since there is currently no drug or therapeutic remedy derived from Korean ginseng, we developed a ginsenoside-enriched fraction (AP-SF) for prevention of various inflammatory symptoms.
Methods: The anti-inflammatory efficacy of AP-SF was tested under in vitro inflammatory conditions including nitric oxide (NO) production and inflammatory gene expression. The molecular events of inflammatory responses were explored by immunoblot analysis.
Results: AP-SF led to a significant suppression of NO production compared with a conventional Korean ginseng saponin fraction, induced by both lipopolysaccharide and zymosan A. Interestingly, AP-SF strongly downregulated the mRNA levels of genes for inducible NO synthase, tumor necrosis factor-a, and cyclooxygenase) without affecting cell viability. In agreement with these observations, AP-SF blocked the nuclear translocation of c-Jun at 2 h and also reduced phosphorylation of p38, c-Jun N-terminal kinase, and TAK-1, all of which are important for c-Jun translocation.
Conclusion: Our results suggest that AP-SF inhibits activation of c-Jun-dependent inflammatory events. Thus, AP-SF may be useful as a novel anti-inflammatory remedy.

목차

abstract
1. Introduction
2. Materials and methods
3. Results and discussion
References

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UCI(KEPA) : I410-ECN-0101-2018-524-001597691