* Graduate Institute of Aerospace and Undersea Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
† Department of Biochemistry, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Am J Chin Med. 2017;45(8):1631-1648. doi: 10.1142/S0192415X17500884. Epub 2017 Nov 9.
Melaleuca alternifolia concentrate (MAC) is the refined essential oil of the Australian native plant Melaleuca alternifolia. MAC has been reported to suppress the production of pro-inflammatory cytokines in both murine RAW264.7 macrophages and human monocytes stimulated with lipopolysaccharide (LPS). However, the mechanisms involved in this effect remain unclear. This study aims to delineate the molecular mechanisms that drive the anti-inflammatory activity of MAC and its active component, terpinen-4-ol, in macrophages. The effects of MAC on RAW264.7 cells were studied using western blotting, real-time PCR, an electrophoretic mobility shift assay (EMSA), and NF-[Formula: see text]B luciferase reporter assays. Our results showed that MAC significantly increased both the mRNA and protein levels of heme oxygenase-1 (HO-1) via p38 and JNK MAPK activation. In addition, we showed that MAC significantly increased the activation and nuclear translocation of NF-E2-related factor 2 (Nrf2), a key transcription factor regulating HO-1 induction. MAC was also associated with significant inhibition of iNOS expression, NO production, and NF-[Formula: see text]B activation. HO-1 was required for these anti-inflammatory effects as tin protoporphyrin IX (SnPPIX), an HO-1 inhibitor, abolished the effects of MAC on LPS-induced iNOS, NO, and NF-[Formula: see text]B activation. Our results indicate that MAC induces HO-1 expression in murine macrophages via the p38 MAPK and JNK pathways and that this induction is required for its anti-inflammatory activity.
互叶白千层浓缩物(MAC)是澳大利亚本土植物互叶白千层的精制精油。据报道,MAC 可抑制脂多糖(LPS)刺激的鼠 RAW264.7 巨噬细胞和人单核细胞中促炎细胞因子的产生。然而,这种作用的机制尚不清楚。本研究旨在阐明驱动 MAC 及其活性成分萜品-4-醇在巨噬细胞中抗炎活性的分子机制。使用 Western blot、实时 PCR、电泳迁移率变动分析(EMSA)和 NF-κB 荧光素酶报告基因测定研究了 MAC 对 RAW264.7 细胞的影响。我们的结果表明,MAC 通过 p38 和 JNK MAPK 激活显着增加血红素加氧酶-1(HO-1)的 mRNA 和蛋白水平。此外,我们表明 MAC 显着增加了核因子-E2 相关因子 2(Nrf2)的激活和核易位,Nrf2 是调节 HO-1 诱导的关键转录因子。MAC 还与 iNOS 表达、NO 产生和 NF-κB 激活的显着抑制有关。HO-1 是这些抗炎作用所必需的,因为血红素加氧酶-1 抑制剂锡原卟啉 IX(SnPPIX)消除了 MAC 对 LPS 诱导的 iNOS、NO 和 NF-κB 激活的影响。我们的结果表明,MAC 通过 p38 MAPK 和 JNK 途径诱导鼠巨噬细胞中 HO-1 的表达,这种诱导是其抗炎活性所必需的。