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Nrf2/HO-1信号通路的激活涉及厚朴酚在牙龈卟啉单胞菌脂多糖刺激的小鼠RAW 264.7巨噬细胞中的抗炎活性。

Activation of Nrf2/HO-1signaling pathway involves the anti-inflammatory activity of magnolol in Porphyromonas gingivalis lipopolysaccharide-stimulated mouse RAW 264.7 macrophages.

作者信息

Lu Sheng-Hua, Hsu Wen-Lin, Chen Tso-Hsiao, Chou Tz-Chong

机构信息

Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan.

School of Medicine, Tzu Chi University, Taiwan; Department of Radiation Oncology, Buddhist Tzu Chi General Hospital, Hualien, Taiwan.

出版信息

Int Immunopharmacol. 2015 Dec;29(2):770-778. doi: 10.1016/j.intimp.2015.08.042. Epub 2015 Sep 18.

Abstract

Magnolol isolated from Magnolia officinalis, a Chinese medical herb, exhibits an anti-inflammatory activity and a protective effect against periodontitis. The inflammation caused by lipopolysaccharide (LPS) from Porphyromonas gingivalis (P. gingivalis) has been considered a key inducer in the development of periodontitis. In this study, we investigated whether magnolol inhibits P. gingivalis LPS-evoked inflammatory responses in RAW 264.7 macrophages and the involvement of heme oxygenase-1 (HO-1). Magnolol significantly activated p38 MAPK, Nrf-2/HO-1 cascade and reactive oxygen species (ROS) formation. Notably, the Nrf-2 activation and HO-1 induction by magnolol were greatly diminished by blocking p38 MAPK activity and ROS production. Furthermore, in P. gingivalis LPS-stimulated macrophages, magnolol treatment remarkably inhibited the inflammatory responses evidenced by suppression of pro-inflammatory cytokine, prostaglandin E2, nitrite formation, and the expression of inducible nitric oxide synthase and cyclooxygenase-2, as well as NF-κB activation accompanied by a significant elevation of Nrf-2 nuclear translocation and HO-1 expression/activity. However, inhibiting HO-1 activity with tin protoporphyrin IX markedly reversed the anti-inflammatory effects of magnolol. Collectively, these findings provide a novel mechanism by which magnolol inhibits P. gingivalis LPS-induced inflammation in macrophages is at least partly mediated by HO-1 activation, and thereby promoting its clinical use in periodontitis.

摘要

从中国草药厚朴中分离出的厚朴酚具有抗炎活性和对牙周炎的保护作用。牙龈卟啉单胞菌(P. gingivalis)的脂多糖(LPS)引起的炎症被认为是牙周炎发展的关键诱因。在本研究中,我们调查了厚朴酚是否抑制P. gingivalis LPS在RAW 264.7巨噬细胞中引发的炎症反应以及血红素加氧酶-1(HO-1)的参与情况。厚朴酚显著激活p38丝裂原活化蛋白激酶(MAPK)、Nrf-2/HO-1级联反应和活性氧(ROS)生成。值得注意的是,通过阻断p38 MAPK活性和ROS生成,厚朴酚对Nrf-2的激活和HO-1的诱导作用大大减弱。此外,在P. gingivalis LPS刺激的巨噬细胞中,厚朴酚处理显著抑制了炎症反应,表现为促炎细胞因子、前列腺素E2、亚硝酸盐生成的抑制,以及诱导型一氧化氮合酶和环氧化酶-2的表达,以及NF-κB的激活,同时伴有Nrf-2核转位和HO-1表达/活性的显著升高。然而,用锡原卟啉IX抑制HO-1活性明显逆转了厚朴酚的抗炎作用。总的来说,这些发现提供了一种新机制,即厚朴酚抑制P. gingivalis LPS诱导的巨噬细胞炎症至少部分是由HO-1激活介导的,从而促进其在牙周炎中的临床应用。

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