Stolarz Amanda J, Farris Ryan A, Wiley Charla A, O'Brien Catherine E, Price Elvin T
Department of Pharmaceutical Sciences, University of Arkansas for Medical, Sciences College of Pharmacy, Little Rock, Arkansas, USA.
Department of Pharmacy Practice, University of Arkansas for Medical, Sciences College of Pharmacy, Little Rock, Arkansas, USA.
Clin Transl Sci. 2015 Dec;8(6):696-701. doi: 10.1111/cts.12310. Epub 2015 Aug 10.
A hallmark of cystic fibrosis (CF) lung disease is neutrophilic airway inflammation. Elevated neutrophil counts have been associated with decreased forced expiratory volume in 1 second and poor clinical measures in patients with CF. Interleukin 8 (IL-8), epithelial neutrophil activating protein 78 (ENA-78), tumor necrosis factor alpha (TNF-α), granulocyte macrophage colony-stimulating factor (GM-CSF), and granulocyte colony-stimulating factor (G-CSF) contribute to neutrophil activation and disease pathogenesis in the airways of patients with CF. Drugs that modify the production of these chemokines in the airways could potentially benefit CF patients. Thus, we determined the effects of fenofibrate on their production in cell populations obtained from the airways. Human small airway epithelial cells and CF bronchial epithelial cells were treated with IL-1β to induce inflammation. We cotreated the cells with fenofibrate at concentrations ranging from 10 to 50 μM to determine if this drug could attenuate the inflammation. IL-8, ENA-78, TNF-α, GM-CSF, and G-CSF production were measured from the cell culture supernates by ELISA. ANOVA statistical testing was conducted using SPSS 17.0. IL-1β increased the production of each of the chemokines by several fold. Fenofibrate reduced IL-1β induced production of each of these neutrophilic chemokines at the concentrations used. IL-1β increases the production of neutrophilic chemokines in airway epithelial cells. Cotreatment with fenofibrate blunts these processes. Fenofibrate should be explored as a therapeutic option to modulate the abundant neutrophilic inflammation observed in CF.
囊性纤维化(CF)肺部疾病的一个标志是中性粒细胞气道炎症。中性粒细胞计数升高与CF患者1秒用力呼气量降低及临床指标不佳有关。白细胞介素8(IL-8)、上皮中性粒细胞激活蛋白78(ENA-78)、肿瘤坏死因子α(TNF-α)、粒细胞巨噬细胞集落刺激因子(GM-CSF)和粒细胞集落刺激因子(G-CSF)在CF患者气道中促使中性粒细胞活化并参与疾病发病机制。能够改变气道中这些趋化因子产生的药物可能会使CF患者受益。因此,我们确定了非诺贝特对从气道获取的细胞群体中这些趋化因子产生的影响。用人白细胞介素1β(IL-1β)处理人小气道上皮细胞和CF支气管上皮细胞以诱导炎症。我们用浓度范围为10至50μM的非诺贝特共同处理这些细胞,以确定该药物是否能减轻炎症。通过酶联免疫吸附测定法(ELISA)从细胞培养上清液中测量IL-8、ENA-78、TNF-α、GM-CSF和G-CSF的产生。使用SPSS 17.0进行方差分析统计检验。IL-1β使每种趋化因子的产生增加了几倍。在所使用的浓度下,非诺贝特降低了IL-1β诱导的这些中性粒细胞趋化因子的产生。IL-1β增加气道上皮细胞中中性粒细胞趋化因子的产生。与非诺贝特共同处理可抑制这些过程。应探索将非诺贝特作为一种治疗选择,以调节CF中观察到的大量中性粒细胞炎症。