| Literature DB >> 30931559 |
Xiang-Dong Su1, Hyun-Jae Jang2, Cai-Yi Wang1, Seung Woong Lee2, Mun-Chual Rho2, Young Ho Kim1, Seo Young Yang1.
Abstract
Four new aster saponins (1-4) together with five known analogues (5-9) were isolated from Aster tataricus. The chemical structures of 1-4 were elucidated based on spectrometric and spectroscopic analysis and comparison with reported data. The potential anti-inflammatory activities of aster saponins 1-9 were evaluated subsequently by measuring lipopolysaccharide (LPS)-enhanced nitric oxide (NO) formation in murine macrophages. Among these, aster saponin B (6) exhibited the most potent inhibitory activity (IC50: 1.2 μM). Additionally, inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) protein levels were dose-dependently suppressed by 6 in LPS-activated RAW 264.7 cells. Investigation of the anti-inflammatory mechanism indicated that 6 attenuated the phosphorylation and degradation of the inhibitor of NF-κB (IκB), which led to the blocking of NF-κB p65 translocation to the nucleus.Entities:
Year: 2019 PMID: 30931559 DOI: 10.1021/acs.jnatprod.8b00856
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050