Department of Microbiology, Pusan National University, Busan 609-735, Republic of Korea.
Bio-IT Fusion Technology Research Institute, Busan, Republic of Korea.
Environ Toxicol Pharmacol. 2012 Sep;34(2):315-323. doi: 10.1016/j.etap.2012.05.001. Epub 2012 May 24.
Recently, it has been reported that several natural extracts have anti-inflammatory effects through HO-1 induction. In this study, we used the ethyl acetate fraction of Bambusae Caulis in Taeniam (BCE) to investigate its anti-inflammatory effect on macrophages stimulated with LPS from Porphyromonas gingivalis. BCE inhibited the production of pro-inflammatory cytokines in P. gingivalis LPS-stimulated RAW264.7 cells. BCE also suppressed the nuclear translocation of NF-κB and AP-1. A selective inhibitor of HO-1 attenuated BCE's inhibitory effects on the production of pro-inflammatory cytokines. BCE also dose-dependently increased HO-1 expression at both the mRNA and the protein levels. BCE increased nuclear translocation of Nrf-2. Finally, a specific inhibitor of p38 reduced BCE-induced HO-1 expression and BCE-induced phosphorylation of p38 MAPK. BCE induced anti-inflammatory effects by activating Nrf-2-mediated HO-1 induction via p38 signaling in P. gingivalis LPS-stimulated macrophages. This result indicates that BCE is a promising therapeutic agent for combating periodontitis.
最近有报道称,几种天然提取物通过诱导 HO-1 具有抗炎作用。在这项研究中,我们使用了 Taeniam 竹茎的乙酸乙酯部分(BCE)来研究其对牙龈卟啉单胞菌 LPS 刺激的巨噬细胞的抗炎作用。BCE 抑制了牙龈卟啉单胞菌 LPS 刺激的 RAW264.7 细胞中促炎细胞因子的产生。BCE 还抑制了 NF-κB 和 AP-1 的核转位。HO-1 的选择性抑制剂减弱了 BCE 对促炎细胞因子产生的抑制作用。BCE 还剂量依赖性地增加了 HO-1 在 mRNA 和蛋白质水平的表达。BCE 增加了 Nrf-2 的核易位。最后,p38 的特异性抑制剂降低了 BCE 诱导的 HO-1 表达和 BCE 诱导的 p38 MAPK 磷酸化。BCE 通过激活 p38 信号通路诱导 Nrf-2 介导的 HO-1 诱导,从而发挥抗炎症作用在牙龈卟啉单胞菌 LPS 刺激的巨噬细胞中。这一结果表明,BCE 是一种有前途的治疗牙周炎的药物。