科研之友
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摘要
Background: Interleukin IL)-1 beta, which is elevated in oral diseases including gingivitis, stimulates epithelial cells to produce IL-8 and perpetuate inflammatory responses. This study investigates stimulatory effects of salivary IL-1 beta in IL-8 production and determines if aloin inhibits IL-1 beta-stimulated IL-8 production in epithelial cells. Methods: Saliva was collected from volunteers to determine IL-1 beta and IL-8 levels. Samples from volunteers were divided into two groups: those with low and those with high IL-1 beta levels. KB cells were stimulated with IL-1 beta or saliva with or without IL-1 receptor agonist or specific mitogen-activated protein kinase MAPK) inhibitors. IL-8 production was measured by enzyme-linked immunosorbent assay ELISA). MAPK protein expression involved in IL-1 beta-induced IL-8 secretion was detected by Western blot. KB cells were pretreated with aloin, and its effect on IL-1 beta-induced IL-8 production was examined by ELISA and Western blot analysis. Results: Saliva with high IL-1 beta strongly stimulated IL-8 production in KB cells, and IL-1 receptor agonist significantly inhibited IL-8 production. Low IL-1 beta-containing saliva did not increase IL-8 production. IL-1 beta treatment of KB cells induced activation of MAPK signaling molecules as well as nuclear factor-kappa B. IL-1 beta-induced IL-8 production was decreased by p38 and extracellular signal-regulated kinase ERK) inhibitor treatment. Aloin pretreatment inhibited IL-1 beta-induced IL-8 production in a dose-dependent manner and inhibited activation of the p38 and ERK signaling pathway. Finally, aloin pretreatment also inhibited saliva-induced IL-8 production. Conclusions: Results indicated that IL-1 beta in saliva stimulates epithelial cells to produce IL-8 and that aloin effectively inhibits salivary IL-1 beta-induced IL-8 production by mitigating the p38 and ERK pathway. Therefore, aloin may be a good candidate for modulating oral inflammatory diseases.
- 出版日期2016-6
