Kim Byung Hun, Lee Yong Gyu, Park Tae Yoon, Kim Ho Bang, Rhee Man Hee, Cho Jae Youl
School of Bioscience and Biotechnology, Kangwon National University, Chuncheon, Korea.
Planta Med. 2009 Mar;75(4):321-6. doi: 10.1055/s-0028-1112218. Epub 2009 Jan 14.
Ginsenoside Rp1 (G-Rp1) is a ginseng saponin derivative with chemopreventive and anti-cancer activities. In this study, we examined the regulatory activity of G-Rp1 on the production of interleukin (IL)-1beta, a pro-inflammatory cytokine managing acute or chronic inflammatory diseases such as septic shock and rheumatoid arthritis, from lipopolysaccharide (LPS)-treated macrophage-like RAW264.7 cells. G-Rp1 dose-dependently inhibited IL-1beta production from LPS-treated RAW264.7 cells without altering cell viability. This compound suppressed both mRNA and protein levels of IL-1beta. In particular, this compound was found to down-regulate phosphorylation of the inhibitor of kappaB (IkappaB) kinase (IKK)/IkappaBalpha, and consequent activation of NF-kappaB, but not the activation of its upstream signaling enzymes such as mitogen-activated protein kinases (MAPK) and p85, a regulatory subunit of phosphoinositide 3-kinase (PI3K). Therefore, these results suggest that G-Rp1 may act as an inhibitor of IL-1beta production by inhibiting the NF-kappaB pathway.
人参皂苷Rp1(G-Rp1)是一种具有化学预防和抗癌活性的人参皂苷衍生物。在本研究中,我们检测了G-Rp1对脂多糖(LPS)处理的巨噬细胞样RAW264.7细胞中白细胞介素(IL)-1β产生的调节活性,IL-1β是一种促炎细胞因子,参与诸如脓毒症休克和类风湿性关节炎等急慢性炎症疾病的发生。G-Rp1剂量依赖性地抑制LPS处理的RAW264.7细胞中IL-1β的产生,且不改变细胞活力。该化合物同时抑制了IL-1β的mRNA和蛋白水平。特别地,发现该化合物可下调κB抑制因子(IkappaB)激酶(IKK)/IkappaBα的磷酸化,以及随后NF-κB的激活,但不影响其上游信号酶如丝裂原活化蛋白激酶(MAPK)和磷酸肌醇3激酶(PI3K)的调节亚基p85的激活。因此,这些结果表明G-Rp1可能通过抑制NF-κB途径而作为IL-1β产生的抑制剂。