Department of Drug Science, Biochemistry Section, University of Catania, Catania, Italy.
Eur Rev Med Pharmacol Sci. 2017 Dec;21(23):5478-5484. doi: 10.26355/eurrev_201712_13938.
In this study we evaluated the possible protective effect of an antioxidant formulation containing microfiltered milk derived polypeptides, Curcumin, Vitamin B2, Carnitine and N-Acetyl-cysteine (NAC) in an in vitro model of chronic obstructive pulmonary disease (COPD).
Human bronchial epithelial cells (16HBE) were used in this study. Cells were treated for 24 h in the presence or absence of 10% of cigarette smoke extract (CSE) and in the presence or absence of antioxidant formulation. We evaluated cell viability by MTT assay, reactive oxygen species by flow cytometer and quantitative analysis of gene expression by Real-time PCR.
The data obtained showed a significant increase of cell viability in CSE-exposed cells and a significant reduction of reactive oxygen species (ROS) production compared to cells treated with only CSE. The antioxidant effects of formulation were confirmed by a decrease of inflammatory cytokines genes IL-1β, IL-6, TNFα, nitric oxide synthase gene (NOS2) and through an induction of antioxidant genes such as heme oxygenase 1 (HO-1), nuclear transcription factor erythroid 2 (NRF2) and peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1α).
The results suggest that antioxidants combination plays a protective role on oxidative stress and inflammation, in an in vitro model of COPD, activating key genes in response to oxidative stress and decreasing the cytokines responsible for the inflammatory pathways.
本研究评估了一种含有微滤牛奶衍生多肽、姜黄素、维生素 B2、肉碱和 N-乙酰半胱氨酸 (NAC) 的抗氧化配方在慢性阻塞性肺疾病 (COPD) 的体外模型中的可能保护作用。
本研究使用人支气管上皮细胞 (16HBE)。细胞在存在或不存在 10%香烟烟雾提取物 (CSE) 的情况下处理 24 小时,并存在或不存在抗氧化剂配方的情况下处理。通过 MTT 测定法评估细胞活力,通过流式细胞仪评估活性氧 (ROS),并通过实时 PCR 进行基因表达的定量分析。
获得的数据显示,与仅用 CSE 处理的细胞相比,CSE 暴露的细胞中细胞活力显著增加,活性氧 (ROS) 产生显著减少。配方的抗氧化作用通过降低炎症细胞因子基因 IL-1β、IL-6、TNFα、一氧化氮合酶基因 (NOS2) 以及诱导抗氧化基因如血红素加氧酶 1 (HO-1)、红细胞 2 核转录因子 (NRF2) 和过氧化物酶体增殖物激活受体 γ共激活因子 1α (PGC-1α) 得到证实。
结果表明,抗氧化剂组合在 COPD 的体外模型中对氧化应激和炎症具有保护作用,激活关键基因以应对氧化应激,并减少炎症途径中负责的细胞因子。