Ginsenoside Rd inhibits the expressions of iNOS and COX-2 by suppressing NF-κB in LPS-stimulated RAW264.7 cells and mouse liver

• Published in: Journal of ginseng research Vol. 37; no. 1; pp. 54 - 63
• Main Authors: Kim, Dae Hyun, Chung, Jae Heun, Yoon, Ji Sung, Ha, Young Mi, Bae, Sungjin, Lee, Eun Kyeong, Jung, Kyung Jin, Kim, Min Sun, Kim, You Jung, Kim, Mi Kyung, Chung, Hae Young
• Format: Journal Article
• Language: English
• Published: Korea (South) The Korean Society of Ginseng 01.03.2013
• Subjects: Prostaglandin E2; Ginsenoside Rd; Cyclooxygenase-2; Panax ginseng; Inducible nitric oxide synthase
• ISSN: 1226-8453; 2093-4947
• DOI: 10.5142/jgr.2013.37.54

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)-κB 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-κB activity; and 4) the NF-κB-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.