| Literature DB >> 27367493 |
Marcelo Franchin1, Pedro Luiz Rosalen1, Marcos Guilherme da Cunha1, Rangel Leal Silva2, David F Colón2, Gabriel Shimizu Bassi2, Severino Matias de Alencar3, Masaharu Ikegaki4, José C Alves-Filho2, Fernando Q Cunha2, John A Beutler5, Thiago Mattar Cunha2.
Abstract
Chemical compounds belonging to the class of coumarins have promising anti-inflammatory potential. Cinnamoyloxy-mammeisin (CNM) is a 4-phenylcoumarin that can be isolated from Brazilian geopropolis. To our knowledge, its anti-inflammatory activity has never been studied. Therefore, the present study investigated the anti-inflammatory activity of CNM and elucidated its mechanism of action on isolated macrophages. Pretreatment with CNM reduced neutrophil migration into the peritoneal and joint cavity of mice. Likewise, CNM reduced the in vitro and in vivo release of TNF-α and CXCL2/MIP-2. Regarding the possible molecular mechanism of action, CNM reduced the phosphorylation of proteins ERK 1/2, JNK, p38 MAPK, and AP-1 (subunit c-jun) in PG-stimulated macrophages. Pretreatment with CNM also reduced NF-κB activation in RAW 264.7 macrophages stably expressing the NF-κB-luciferase reporter gene. On the other hand, it did not alter IκBα degradation or nuclear translocation of p65. Thus, the results of this study demonstrate promising anti-inflammatory activity of CNM and provide an explanation of its mechanism of action in macrophages via inhibition of MAPK signaling, AP-1, and NF-κB.Entities:
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Year: 2016 PMID: 27367493 PMCID: PMC7757851 DOI: 10.1021/acs.jnatprod.6b00263
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050