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논문 기본 정보

자료유형
학술저널
저자정보
Fu Li (Chinese Academy of Sciences) Yufeng Cao (Huaiyin Normal University) Yanyan Luo (Huaiyin Normal University) Tingwu Liu (Huaiyin Normal University) Guilong Yan (Huaiyin Normal University) Liang Chen (Huaiyin Normal University) Lilian Ji (Huaiyin Normal University) Lun Wang (Chinese Academy of Sciences) Bin Chen (Chinese Academy of Sciences) Aftab Yaseen (Chinese Academy of Sciences) Ashfaq A. Khan (Women University of Azad Jammu and Kashmir) Guolin Zhang (Chinese Academy of Sciences) Yunyao Jiang (China Academy of Chinese Medical Sciences) Jianxun Liu (China Academy of Chinese Medical Sciences) Gongcheng Wang (Nanjing Medical University) Ming-Kui Wang (Chinese Academy of Sciences) Weicheng Hu (Huaiyin Normal University)
저널정보
고려인삼학회 Journal of Ginseng Research Journal of Ginseng Research Vol.43 No.4
발행연도
2019.10
수록면
600 - 605 (6page)

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Background: The leaves and roots of Panax ginseng are rich in ginsenosides. However, the chemical compositions of the leaves and roots of P. ginseng differ, resulting in different medicinal functions. In recent years, the aerial parts of members of the Panax genus have received great attention from natural product chemists as producers of bioactive ginsenosides. The aim of this study was the isolation and structural elucidation of novel, minor ginsenosides in the leaves of P. ginseng and evaluation of their antiinflammatory activity in vitro.
Methods: Various chromatographic techniques were applied to obtain pure individual compounds, and their structures were determined by nuclear magnetic resonance and high-resolution mass spectrometry, as well as chemical methods. The antiinflammatory effect of the new compounds was evaluated on lipopolysaccharide-stimulated RAW 264.7 cells.
Results and conclusions: Two novel, minor triterpenoid saponins, ginsenoside LS₁ (1) and 5,6-didehydroginsenoside Rg₃ (2), were isolated from the leaves of P. ginseng. The isolated compounds 1 and 2 were assayed for their inhibitory effect on nitric oxide production in LPS-stimulated RAW 264.7 cells, and Compound 2 showed a significant inhibitory effect with IC<SUB>50</SUB> of 37.38 µM compared with that of NG-monomethyl-L-arginine (IC<SUB>50</SUB> = 90.76 µM). Moreover, Compound 2 significantly decreased secretion of cytokines such as prostaglandin E₂ and tumor necrosis factor-a. In addition, Compound 2 significantly suppressed protein expression of inducible nitric oxide synthase and cyclooxygenase-2. These results suggested that Compound 2 could be used as a valuable candidate for medicinal use or functional food, and the mechanism is warranted for further exploration.

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

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