University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Cardiovasc Drugs Ther. 2012 Apr;26(2):95-9. doi: 10.1007/s10557-011-6368-7.
The PPAR-alpha agonists (fibrates) are commonly used in the treatment of dyslipidemia. It has been hypothesized that the cardio-protective effects of fibrates are partially due to immunomodulatory effects. However, there is a paucity of data regarding the effect of fibrates on neutrophilic chemokines such as epithelial neutrophil activating protein (ENA-78) and interleukin (IL)-8. We investigated the influence of fenofibrate on IL-1β-stimulated production of ENA-78 and IL-8 from human endothelial cells (HUVECs).
HUVECs were cultured in the presence or absence of IL-1β and fenofibrate ranging from 1-50 uM. ENA-78 and IL-8 were measured and normalized to total protein content in cell culture supernates by multiplex immunofluorescence detection. Experimental samples were measured in triplicate. Significance was set at P < 0.05 by ANOVA with correction for multiple comparisons.
Endothelial production of both ENA-78 and IL-8 was induced by the proinflammatory cytokine IL-1β. ENA-78 concentrations increased by more than 160-fold over constitutively produced ENA-78 upon IL-1β stimulation (mean ± SEM: 10,129 ± 1591 pg/mg vs. 61 ± 9.5 mg/mg; P < 0.0001). IL-8 concentrations increased by slightly over 5-fold (6145 ± 860 pg/mg vs. 1160 ± 201 pg/mg; P = 0.0003). ENA-78 protein and mRNA were significantly reduced by fenofibrate while no drug effects were observed on IL-8 production.
Fenofibrate blunts IL-1β-mediated ENA-78 production with no effect on IL-8. This represents a novel mechanism by which fenofibrate exerts anti-inflammatory effects and should be further explored.
过氧化物酶体增殖物激活受体-α 激动剂(贝特类药物)常用于治疗血脂异常。据推测,贝特类药物的心脏保护作用部分归因于免疫调节作用。然而,关于贝特类药物对中性粒细胞趋化因子(如上皮中性粒细胞激活蛋白[ENA-78]和白细胞介素[IL]-8)的影响的数据很少。我们研究了非诺贝特对人内皮细胞(HUVEC)中 IL-1β 刺激产生的 ENA-78 和 IL-8 的影响。
在存在或不存在 IL-1β 和非诺贝特(1-50 μM)的情况下培养 HUVEC。通过多重免疫荧光检测测量 ENA-78 和 IL-8,并将其归一化为细胞培养上清液中的总蛋白含量。实验样品一式三份测量。通过方差分析(校正多重比较后),以 P < 0.05 为显著性标准。
促炎细胞因子 IL-1β 诱导内皮细胞产生 ENA-78 和 IL-8。ENA-78 浓度在 IL-1β 刺激后比基础产生的 ENA-78 增加了 160 多倍(平均值 ± SEM:10129 ± 1591 pg/mg 比 61 ± 9.5 mg/mg;P < 0.0001)。IL-8 浓度增加略超过 5 倍(6145 ± 860 pg/mg 比 1160 ± 201 pg/mg;P = 0.0003)。非诺贝特显著降低 ENA-78 蛋白和 mRNA,但对 IL-8 产生无药物作用。
非诺贝特可减弱 IL-1β 介导的 ENA-78 产生,而对 IL-8 无影响。这代表了非诺贝特发挥抗炎作用的一种新机制,应进一步探索。