Chen Jian-Yu, Zhu Guo-Yuan, Su Xiao-Hui, Wang Rui, Liu Juan, Liao Kangsheng, Ren Rutong, Li Ting, Liu Liang
State Key Laboratory of Quality Research in Chinese Medicine, Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Macau, China.
Oncotarget. 2017 Jul 5;8(33):55051-55063. doi: 10.18632/oncotarget.19017. eCollection 2017 Aug 15.
Macrophages play a critical role in a variety of inflammatory diseases. Activation of Keap1/Nrf2/HO-1 signaling results in inactivation of macrophages and amelioration of inflammatory and autoimmune conditions. Hence, discovery for the activators of Keap1/Nrf2/HO-1 signaling has become a promising strategy for treatment inflammatory diseases. In the current study, the anti-inflammatory potential of 7-deacetylgedunin (7-DGD), a limonin chemical isolated from the fruits of (A. Juss.) Roem, was intensively examined and for the first time. Results showed that 7-DGD alleviated mice mortality induced by LPS. Mechanistic study showed that 7-DGD suppressed macrophage proliferation induction of cell arrest at the G0/G1 phase. Furthermore, 7-DGD inhibited iNOS expression, which is correlated with the increases of NQO1, HO-1 and UGT1A1 mRNA expression as well as HO-1 protein expression level in the cells. More importantly, 7-DGD markedly decreased Keap1 expression, promoted p62 expression, and facilitated Nrf2 translocation and localization in the nucleus of macrophages, and in turn up-regulates these anti-oxidant enzymes expression, eventually mediated anti-inflammatory effect. Collectively, 7-DGD suppresses inflammation and , indicating that the compound is valuable for further investigation as an anti-inflammatory agent in future.
巨噬细胞在多种炎症性疾病中起关键作用。Keap1/Nrf2/HO-1信号通路的激活会导致巨噬细胞失活,并改善炎症和自身免疫状况。因此,寻找Keap1/Nrf2/HO-1信号通路的激活剂已成为治疗炎症性疾病的一种有前景的策略。在本研究中,首次深入研究了从印楝(Azadirachta indica A. Juss.)果实中分离出的柠檬苦素类化合物7-脱乙酰格杜宁(7-DGD)的抗炎潜力。结果表明,7-DGD可减轻LPS诱导的小鼠死亡率。机制研究表明,7-DGD抑制巨噬细胞增殖,诱导细胞停滞于G0/G1期。此外,7-DGD抑制诱导型一氧化氮合酶(iNOS)表达,这与细胞中醌氧化还原酶1(NQO1)、血红素加氧酶-1(HO-1)和尿苷二磷酸葡萄糖醛酸基转移酶1A1(UGT1A1)mRNA表达的增加以及HO-1蛋白表达水平相关。更重要的是,7-DGD显著降低Keap1表达,促进p62表达,并促进Nrf2在巨噬细胞核中的转位和定位,进而上调这些抗氧化酶的表达,最终介导抗炎作用。总体而言,7-DGD抑制炎症反应,表明该化合物作为一种抗炎剂在未来有进一步研究的价值。