Chokpaisarn Julalak, Urao Norifumi, Voravuthikunchai Supayang P, Koh Timothy J
Department of Microbiology and Excellent Research Laboratory on Natural Products, Faculty of Science and Natural Product Research Center of Excellence, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand.
Department of Kinesiology and Nutrition, University of Illinois at Chicago, Chicago, IL 60612, USA.
Cytokine. 2017 Jun;94:29-36. doi: 10.1016/j.cyto.2017.04.005. Epub 2017 Apr 11.
Chronic inflammation plays a key role in the pathogenesis of myriad complications associated with diabetes and thus anti-inflammatory therapies may ameliorate these complications. Quercus infectoria (Qi) extract has been shown to downregulate inflammatory processes; however, the molecular mechanisms of this anti-inflammatory activity remain unclear. The hypothesis of our study was that Qi extract exerts its anti-inflammatory effect by downregulating the Set7/NF-κB pathway. Bone marrow-derived macrophages (BMM) were treated with high glucose plus palmitate medium (HG/Pa) to simulate the diabetic environment. Compared with control conditions, HG/Pa elevated expression Set7, expression and activity of NF-κB along with expression of several inflammatory cytokines. These changes were associated with increased levels of intracellular reactive oxygen species (ROS). Moreover, similar alterations were demonstrated in BMM derived from mice fed a high fat diet (HFD) compared to those from lean mice, suggesting that HFD-induced changes in BM progenitors persist throughout differentiation and culture. Importantly, Qi extract dose-dependently reduced Set7, p65 and inflammatory cytokine expression relative to vehicle controls in both HG/Pa-and HFD-treated BMM. Finally, macrophages/monocytes isolated from wounds of diabetic mice that were treated with Qi solution exhibited lower expression of the inflammatory cytokines, IL-1β and TNF-α, compared with vehicle treated wounds, demonstrating translation to the in vivo diabetic environment. Taken together, data from this study suggests that Qi downregulates diabetes-induced activity of the Set7/NF-kB pathway.
慢性炎症在糖尿病相关的众多并发症发病机制中起关键作用,因此抗炎疗法可能改善这些并发症。没食子提取物已被证明可下调炎症过程;然而,这种抗炎活性的分子机制仍不清楚。我们研究的假设是没食子提取物通过下调Set7/核因子-κB(NF-κB)途径发挥其抗炎作用。用高糖加棕榈酸培养基(HG/Pa)处理骨髓来源的巨噬细胞(BMM)以模拟糖尿病环境。与对照条件相比,HG/Pa提高了Set7的表达、NF-κB的表达和活性以及几种炎性细胞因子的表达。这些变化与细胞内活性氧(ROS)水平升高有关。此外,与瘦小鼠来源的BMM相比,高脂饮食(HFD)喂养的小鼠来源的BMM也表现出类似的变化,这表明HFD诱导的骨髓祖细胞变化在整个分化和培养过程中持续存在。重要的是,在HG/Pa处理和HFD处理的BMM中,相对于载体对照,没食子提取物剂量依赖性地降低了Set7、p65和炎性细胞因子的表达。最后,与载体处理的伤口相比,用没食子溶液处理的糖尿病小鼠伤口分离的巨噬细胞/单核细胞表现出较低的炎性细胞因子白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)表达,证明了在体内糖尿病环境中的转化。综上所述,本研究数据表明没食子下调糖尿病诱导的Set7/NF-κB途径活性。