D(-)-Salicin inhibits the LPS-induced inflammation in RAW264.7 cells and mouse models
D(-)-Salicin inhibits the LPS-induced inflammation in RAW264.7 cells and mouse models
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D(-)-Salicin 抑制 RAW264.7 细胞和小鼠模型中 LPS 诱导的炎症
DOI:
10.1016/j.intimp.2015.04.016
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发表时间:
2015-06-01
影响因子:
5.6
通讯作者:
Feng, Haihua
中科院分区:
文献类型:
--
作者:
Li, Yang;Wu, Qianchao;Feng, Haihua
D(-)-Salicin is a traditional medicine which has been known to exhibit anti-inflammation and other therapeutic activities. The present study aimed to investigate whether D(-)-Salicin inhibited the LPS-induced inflammation in vivo and in vitro. We evaluated the effect of D(-)-Salicin on cytokines (TNF-alpha, IL-1 beta, IL-6 and IL-10) in vivo and in vitro by enzyme-linked immunosorbent assay and signaling pathways (MAPKs and NF-kappa B) in vivo by Western blot. The results showed that D(-)-Salicin markedly decreased TNF-alpha, IL-1 beta and IL-6 concentrations and increased IL-10 concentration. In addition, western blot analysis indicated that D(-)-Salicin suppressed the activation of MAPKs and NF-kappa B signaling pathways stimulated by LPS. To examine whether D(-)-Salicin ameliorated LPS-induced lung inflammation, inhibitors of MAPKs and NF-kappa B signaling pathways were administrated intraperitoneally to mice. Interference with specific inhibitors revealed that D(-)-Salicin-mediated cytokine suppression was through MAPKs and NF-kappa B pathways. In the mouse model of acute lung injury, histopathologic examination indicted that D(-)-Salicin suppressed edema induced by LPS. So it is suggest that D(-)-Salicin might be a potential therapeutic agent against inflammatory diseases. (C) 2015 Elsevier B.V. All rights reserved.