Yang Hailing, Li Yan, Huo Pengfei, Li Xiao-Ou, Kong Daliang, Mu Wei, Fang Wei, Li Lingxia, Liu Ning, Fang Ling, Li Hongjun, He Chengyan
Emergency Department, Jilin University, Changchun 130041, China.
Intensive Care Unit, Jilin University, Changchun 130041, China.
Int Immunopharmacol. 2015 May;26(1):119-24. doi: 10.1016/j.intimp.2015.03.021. Epub 2015 Mar 27.
Jolkinolide B (JB), an ent-abietane diterpenoid, isolated from the dried root of Euphorbia fischeriana, has been reported to have potent anti-tumor and anti-inflammatory activities. However, the effects of JB on acute lung injury (ALI) and underlying molecular mechanisms have not been investigated. The present study aimed to investigate the effect of JB on lipopolysaccharide (LPS)-induced ALI. Male C57BL/6 mice were pretreated with dexamethasone or JB 1h before intranasal instillation of LPS. The results showed that JB markedly attenuated LPS-induced histological alterations, lung edema, inflammatory cell infiltration, myeloperoxidase (MPO) activity as well as the production of TNF-α, IL-6 and IL-1β. Furthermore, JB also significantly inhibited LPS-induced the degradation of IκBα and phosphorylation of NF-κB p65 and MAPK. Therefore, our study provides the first line of evidence that pretreatment of JB has a protective effect on LPS-induced ALI in mice. The anti-inflammatory mechanism of JB may be attributed to its suppression of NF-κB and MAPK activation.
jolkinolide B(JB)是一种从狼毒大戟干燥根中分离得到的对映贝壳杉烷二萜,据报道具有强大的抗肿瘤和抗炎活性。然而,JB对急性肺损伤(ALI)的影响及其潜在的分子机制尚未得到研究。本研究旨在探讨JB对脂多糖(LPS)诱导的ALI的影响。雄性C57BL/6小鼠在鼻内滴注LPS前1小时用 dexamethasone或JB进行预处理。结果表明,JB显著减轻了LPS诱导的组织学改变、肺水肿、炎症细胞浸润、髓过氧化物酶(MPO)活性以及TNF-α、IL-6和IL-1β的产生。此外,JB还显著抑制了LPS诱导的IκBα降解以及NF-κB p65和MAPK的磷酸化。因此,我们的研究提供了首个证据,即JB预处理对LPS诱导的小鼠ALI具有保护作用。JB的抗炎机制可能归因于其对NF-κB和MAPK激活的抑制作用。