Department of Anatomy and Histology and Embryology, Yanbian University Medical College, Yanji, 133002, P.R. China.
Department of Respiratory Medicine, Yanbian University Hospital, Yanji, P.R. China.
Sci Rep. 2017 Sep 19;7(1):11895. doi: 10.1038/s41598-017-12252-3.
Polydatin(PD) shows anti-allergic inflammatory effect, and this study investigated its underlying mechanisms in in vitro and in vivo models. IgE-mediated passive cutaneous anaphylaxis (PCA) and passive systemic anaphylaxis (PSA) models were used to confirm PD effect in vivo. Various signaling pathway proteins in mast cell were examined. RT-PCR, ELISA and western blotting were applied when appropriate. Activity of Lyn and Fyn kinases in vitro was measured using the Kinase Enzyme System. PD dose-dependently reduced the pigmentation of Evans blue in the PCA model and decreased the concentration of serum histamine in PSA model, and attenuated the degranulation of mast cells without generating cytotoxicity. PD decreased pro-inflammatory cytokine expression (TNF-α, IL-4, IL-1β, and IL-8). PD directly inhibited activity of Lyn and Syk kinases and down-regulated downstream signaling pathway including MAPK, PI3K/AKT and NF-kB. In addition, PD also targets Nrf2/HO-1 pathway to inhibit mast cell-derived allergic inflammatory reactions. In conclusion, the study demonstrates that PD is a possible therapeutic candidate for allergic inflammatory diseases. It directly inhibited activity of Lyn and Syk kinases and down-regulates the signaling pathway of MAPK, PI3K/AKT and NF-κB, and up-regulates the signaling pathway of Nrf2/HO-1 to inhibit the degranulation of mast cells.
虎杖苷(PD)具有抗过敏炎症作用,本研究在体外和体内模型中探讨了其潜在机制。使用 IgE 介导的被动皮肤过敏反应(PCA)和被动全身过敏反应(PSA)模型来确认 PD 在体内的作用。检查肥大细胞中各种信号通路蛋白。当适当时,应用 RT-PCR、ELISA 和 Western blotting。使用激酶酶系统测量体外 Lyn 和 Fyn 激酶的活性。PD 剂量依赖性地降低 PCA 模型中 Evans 蓝的着色,并降低 PSA 模型中血清组织胺的浓度,并且在不产生细胞毒性的情况下减弱肥大细胞的脱颗粒作用。PD 降低促炎细胞因子的表达(TNF-α、IL-4、IL-1β 和 IL-8)。PD 直接抑制 Lyn 和 Syk 激酶的活性,并下调包括 MAPK、PI3K/AKT 和 NF-κB 在内的下游信号通路。此外,PD 还针对 Nrf2/HO-1 途径抑制肥大细胞来源的过敏炎症反应。总之,该研究表明 PD 是治疗过敏炎症性疾病的潜在候选药物。它直接抑制 Lyn 和 Syk 激酶的活性,并下调 MAPK、PI3K/AKT 和 NF-κB 的信号通路,上调 Nrf2/HO-1 的信号通路以抑制肥大细胞的脱颗粒作用。