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논문 기본 정보

자료유형
학술저널
저자정보
Taddessee Yayeh (Kyungpook National University) Kun-Ho Jung (Chungnam National University) Hye Yoon Jeong (Sungkyunkwan University) Ji-Hoon Park (Kyungpook National University) Yong-Bum Song (Ginseng Corporation Central Research Institute) Yi-Seong Kwak (Corporation Central Research Institute) Heun-Soo Kang (Metabolab) Jae-Youl Cho (Sungkyunkwan University) Jae-Wook Oh (Konkuk University) Sang-Keun Kim (Chungnam National University) Man Hee Rhee (Kyungpook National University)
저널정보
고려인삼학회 Journal of Ginseng Research Journal of Ginseng Research Vol.36 No.3
발행연도
2012.7
수록면
263 - 269 (7page)

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초록· 키워드

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Korean red ginseng has shown therapeutic effects for a number of disease conditions. However, little is known about the anti-inflammatory effect of Korean red ginseng saponin fraction (RGSF) in vitro and vivo. Therefore, in this study, we showed that RGSF containing 20(s)-protopanaxadiol type saponins inhibited nitric oxide production and attenuated the release of tumor necrotic factor (TNF)-α, interleukin (IL)-6, granulocyte monocyte colony stimulating factor (GMCSF), and macrophage chemo-attractant protein-1 in lipopolysaccharide (LPS) stimulated murine macrophage RAW264.7 cells. Moreover, RGSF down-regulated the mRNA expressions of inducible nitric oxide synthase, cyclooxyginase-2, IL-1β, TNF-α GMCSF, and IL-6. Furthermore, RGSF reduced the level of TNF-α in the serum and protected mice against LPS mediated endotoxic shock. In conclusion, these results indicated that ginsenosides from RGSF and their metabolites could be potential sources of therapeutic agents against inflammation.

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INTRODUCTION
MATERIALS AND METHODS
RESULTS AND DISCUSSION
ACKNOWLEDGEMENT
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2013-524-003639905