| Literature DB >> 30108912 |
Jun-Xia Zheng1, Yu-Shui Han2, Jin-Cai Wang2, Hui Yang2, Hao Kong2, Kang-Jia Liu2, Si-Yu Chen2, Yi-Rui Chen3, Yi-Qun Chang2, Wei-Min Chen2, Jia-Liang Guo3, Ping-Hua Sun2.
Abstract
Strigolactones (SLs) are a novel class of plant hormones with enormous potential for the prevention and treatment of inflammation. To further investigate the anti-inflammatory activities of SLs, a representative SL, GR24, and the reductive products of its D-ring were synthesized and their anti-inflammatory activities were fully evaluated on both in vitro and in vivo models. Among these compounds, the two most active optical isomers (2a and 6a) demonstrated strong inhibitory activity on the release of inflammatory cytokines, including nitric oxide (NO), tumor necrosis factor-alpha (TNF-α), and interleukin-6 (IL-6) by blocking the nuclear factor kappa B (NF-κB) and mitogen-activated protein kinase (MAPK) signaling pathways; they also greatly inhibited the migration of neutrophils and macrophages in fluorescent protein labeled zebrafish larvae. These results identified the promising anti-inflammatory effects of SLs, and suggested that both the absolute configuration of SL and the α,β-unsaturated D-ring structure are essential for the observed anti-inflammatory activity.Entities:
Year: 2017 PMID: 30108912 PMCID: PMC6072207 DOI: 10.1039/c7md00461c
Source DB: PubMed Journal: Medchemcomm ISSN: 2040-2503 Impact factor: 3.597