Franchin Marcelo, Rosalen Pedro Luiz, da Cunha Marcos Guilherme, Silva Rangel Leal, Colón David F, Bassi Gabriel Shimizu, de Alencar Severino Matias, Ikegaki Masaharu, Alves-Filho José C, Cunha Fernando Q, Beutler John A, Cunha Thiago Mattar
Piracicaba Dental School, University of Campinas , Piracicaba, 13414-903, SP, Brazil.
Ribeirão Preto Medical School, University of São Paulo , Ribeirão Preto, 14049-900, SP, Brazil.
J Nat Prod. 2016 Jul 22;79(7):1828-33. doi: 10.1021/acs.jnatprod.6b00263. Epub 2016 Jul 1.
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.
属于香豆素类的化合物具有良好的抗炎潜力。肉桂酰氧基-马米辛(CNM)是一种可从巴西蜂胶中分离得到的4-苯基香豆素。据我们所知,其抗炎活性从未被研究过。因此,本研究调查了CNM的抗炎活性,并阐明了其对分离的巨噬细胞的作用机制。用CNM预处理可减少中性粒细胞向小鼠腹腔和关节腔的迁移。同样,CNM降低了TNF-α和CXCL2/MIP-2在体外和体内的释放。关于可能的分子作用机制,CNM降低了PG刺激的巨噬细胞中ERK 1/2、JNK、p38 MAPK和AP-1(亚基c-jun)蛋白的磷酸化。用CNM预处理还降低了稳定表达NF-κB-荧光素酶报告基因的RAW 264.7巨噬细胞中NF-κB的激活。另一方面,它没有改变IκBα的降解或p65的核转位。因此,本研究结果证明了CNM具有良好的抗炎活性,并通过抑制MAPK信号传导、AP-1和NF-κB解释了其在巨噬细胞中的作用机制。