Department of Pharmacology for Chinese Materia Medica, China Pharmaceutical University, 639 Long Mian Avenue, Nanjing 211198, China.
Biochimie. 2010 Jul;92(7):789-96. doi: 10.1016/j.biochi.2010.02.024. Epub 2010 Feb 25.
Resveratrol is a potent inhibitor of inflammation and has anti-diabetic potentiality, however whether its anti-inflammatory potency contributes to the amelioration of diabetes or insulin resistance remains to be determined. This study aims at evaluating the effects of resveratrol on inflammation-related adipokines expression and insulin sensitivity in adipocytes. We stimulated RAW264.7 cells with LPS and collected the supernatant as a conditioned medium (CM) for the culture of adipocytes. Resveratrol, at concentrations ranging from 0.1 to 10 muM, effectively inhibited lipopolysaccharide (LPS)-induced TNF-alpha and IL-6 production with the downregulation of relative genes expression in macrophages. Exposing differentiated 3T3-L1 cells to RAW264.7 CM resulted in gene over-expressions of TNF-alpha, IL-6 and resistin, however, mRNA expression of adiponectin and PPARgamma were down-regulated. Pretreatment of CM from resveratrol-treated macrophages reduced the elevated levels of TNF-alpha and IL-6, and significantly reversed inflammation-related changes in adipokine gene expression in 3T3-L1 adipocytes. Resveratrol suppressed extracellular receptor-activated kinase (ERK) and transcription factor-kappaB (NF-kappaB) activation by reducing the phosphorylation of ERK1/2 and NF-kappaB p65; moreover, it modulated insulin signaling transduction by modification of Ser/Thr phosphorylation of insulin receptor substrate-1 (IRS-1) and downstream AKT (T308), and thereby improved insulin sensitivity in adiposities. These results demonstrated that resveratrol modulated adipokines expression and improved insulin sensitivity which relative to inhibition of inflammatory-like response in adipocytes.
白藜芦醇是一种有效的炎症抑制剂,具有抗糖尿病的潜力,然而,其抗炎作用是否有助于改善糖尿病或胰岛素抵抗仍有待确定。本研究旨在评估白藜芦醇对脂肪细胞中与炎症相关的脂肪因子表达和胰岛素敏感性的影响。我们用 LPS 刺激 RAW264.7 细胞,并收集上清液作为条件培养基(CM)用于脂肪细胞的培养。白藜芦醇在 0.1 至 10 μM 的浓度范围内有效抑制脂多糖(LPS)诱导的 TNF-α和 IL-6 的产生,并下调巨噬细胞中相关基因的表达。将分化的 3T3-L1 细胞暴露于 RAW264.7 CM 中,导致 TNF-α、IL-6 和抵抗素的基因过度表达,而脂联素和 PPARγ的 mRNA 表达则下调。用白藜芦醇处理的巨噬细胞的 CM 预处理可降低 TNF-α和 IL-6 的升高水平,并显著逆转 3T3-L1 脂肪细胞中与炎症相关的脂肪因子基因表达的变化。白藜芦醇通过降低 ERK1/2 和 NF-κB p65 的磷酸化来抑制细胞外受体激活激酶(ERK)和转录因子-κB(NF-κB)的激活;此外,它通过修饰胰岛素受体底物-1(IRS-1)和下游 AKT(T308)的丝氨酸/苏氨酸磷酸化来调节胰岛素信号转导,从而改善脂肪组织中的胰岛素敏感性。这些结果表明,白藜芦醇调节脂肪因子的表达并改善胰岛素敏感性,这与抑制脂肪细胞中的炎症样反应有关。