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논문 기본 정보

자료유형
학술저널
저자정보
Dae Hyun Kim (Pusan National University) Jae Heun Chung (Pusan National University) Ji Sung Yoon (Pusan National University) Young Mi Ha (Pusan National University) Sungjin Bae (Pusan National University) Eun Kyeong Lee (Dongnam Institute of Radiological and Medical Sciences) Kyung Jin Jung (Korea Institute of Toxicology) Min Sun Kim (Sunchon National University) You Jung Kim (Busan Women’s College) Mi Kyung Kim (Pusan National University) Hae Young Chung (Pusan National University)
저널정보
고려인삼학회 Journal of Ginseng Research Journal of Ginseng Research Vol.37 No.1
발행연도
2013.1
수록면
54 - 63 (10page)

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초록· 키워드

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Ginsenoside Rd is a primary constituent of the ginseng rhizome and has been shown to participate in the regulation of diabetes and in tumor formation. Reports also show that ginsenoside Rd exerts anti-oxidative effects by activating anti-oxidant enzymes. Treatment with ginsenoside Rd decreased nitric oxide and prostaglandin E2 (PGE2) in lipopolysaccharides (LPS)-challenged RAW264.7 cells and in ICR mouse livers (5 mg/kg LPS; LPS + ginsenoside Rd [2, 10, and 50 mg/kg]). Furthermore, these decreases were associated with the down-regulations of inducible nitric oxide synthase (iNOS) and cyclooxygenase (COX)-2 and of nuclear factor (NF)-kB activity in vitro and in vivo. Our results indicate that ginsenoside Rd treatment decreases; 1) nitric oxide production (40% inhibition); 2) PGE2 synthesis (69% to 93% inhibition); 3) NF-kB activity; and 4) the NF-kB-regulated expressions of iNOS and COX-2. Taken together, our results suggest that the anti-inflammatory effects of ginsenoside Rd are due to the down-regulation of NF-κB and the consequent expressional suppressions of iNOS and COX-2.

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INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2014-524-000316398