Saavedra Nicolás, Cuevas Alejandro, Cavalcante Marcela F, Dörr Felipe A, Saavedra Kathleen, Zambrano Tomás, Abdalla Dulcineia S P, Salazar Luis A
Center of Molecular Biology and Pharmacogenetics, Department of Basic Sciences, Scientific and Technological Bioresource Nucleus, Universidad de La Frontera, Avenida Francisco Salazar 01145, 4811230 Temuco, Chile.
Department of Clinical and Toxicological Analyses, Faculty of Pharmaceutical Sciences, Universidade de São Paulo, Avenida Professor Lineu Prestes 580, 05508-000 São Paulo, SP, Brazil.
Biomed Res Int. 2016;2016:6505383. doi: 10.1155/2016/6505383. Epub 2016 Mar 28.
Polyphenols from diverse sources have shown anti-inflammatory activity. In the context of atherosclerosis, macrophages play important roles including matrix metalloproteinases synthesis involved in degradation of matrix extracellular components affecting the atherosclerotic plaque stability. We prepared a propolis extract and pinocembrin in ethanol solution. Propolis extract was chemically characterized using LC-MS. The effect of treatments on gene expression and proteolytic activity was measured in vitro using murine macrophages activated with LPS. Cellular toxicity associated with both treatments and the vehicle was determined using MTT and apoptosis/necrosis detection assays. MMP-9 gene expression and proteolytic activity were measured using qPCR and zymography, respectively. Thirty-two compounds were identified in the propolis extract, including pinocembrin among its major components. Treatment with either ethanolic extract of propolis or pinocembrin inhibits MMP-9 gene expression in a dose-dependent manner. Similarly, an inhibitory effect was observed in proteolytic activity. However, the effect showed by ethanolic extract of propolis was higher than the effect of pinocembrin, suggesting that MMP-9 inhibition results from a joint contribution between the components of the extract. These data suggest a potential role of polyphenols from Chilean propolis in the control of extracellular matrix degradation in atherosclerotic plaques.
来自不同来源的多酚已显示出抗炎活性。在动脉粥样硬化的背景下,巨噬细胞发挥着重要作用,包括合成参与降解细胞外基质成分的基质金属蛋白酶,这会影响动脉粥样硬化斑块的稳定性。我们制备了蜂胶提取物和松属素的乙醇溶液。蜂胶提取物通过液相色谱 - 质谱联用进行化学表征。使用脂多糖激活的小鼠巨噬细胞在体外测量处理对基因表达和蛋白水解活性的影响。使用MTT和凋亡/坏死检测试验确定与两种处理及溶剂相关的细胞毒性。分别使用定量聚合酶链反应和酶谱法测量基质金属蛋白酶 - 9(MMP - 9)的基因表达和蛋白水解活性。在蜂胶提取物中鉴定出32种化合物,其中主要成分包括松属素。用蜂胶乙醇提取物或松属素处理均以剂量依赖性方式抑制MMP - 9基因表达。同样,在蛋白水解活性方面也观察到抑制作用。然而,蜂胶乙醇提取物显示的效果高于松属素,这表明MMP - 9的抑制是提取物成分共同作用的结果。这些数据表明智利蜂胶中的多酚在控制动脉粥样硬化斑块中细胞外基质降解方面具有潜在作用。