Albuquerque K F F S, Marinovic M P, Morandi A C, Bolin A P, Otton R
Department of Pharmacology, Biomedical Sciences Institute, University of São Paulo, São Paulo, Brazil.
Postgraduate Programme, Health Sciences, CBS, Universidade Cruzeiro do Sul, São Paulo, São Paulo, Brazil.
Eur J Nutr. 2016 Apr;55(3):1261-74. doi: 10.1007/s00394-015-0940-z. Epub 2015 Jun 2.
Our study aimed to evaluate whether obesity induced by cafeteria diet changes the neutrophil effector/inflammatory function and whether treatment with green tea extract (GT) can improve neutrophil function.
Male Wistar rats were treated with GT by gavage (12 weeks/5 days/week; 500 mg/kg of body weight), and obesity was induced by cafeteria diet (8 weeks). Neutrophils were obtained from the peritoneal cavity (injection of oyster glycogen). The following analyses were performed: phagocytic capacity, chemotaxis, myeloperoxidase activity (MPO), hypochlorous acid (HOCl), superoxide anion (O 2 (·-) ), hydrogen peroxide (H2O2), IL-1β, IL-6 and TNFα, mRNA levels of inflammatory genes, calcium mobilisation, activities of antioxidant enzymes, hexokinase and G6PDH.
Neutrophils from obese rats showed a significant decrease in migration capacity, H2O2 and HOCl production, MPO activity and O 2 (·-) production. Phagocytosis and CD11b mRNA levels were increased, while inflammatory cytokines release remained unmodified. mRNA levels of TLR4 and IκK were enhanced. Treatment of obese rats with GT increased neutrophil migration, MPO activity, H2O2, HOCl and O 2 (·-) production, whereas TNF-α and IL-6 were decreased (versus obese). Similar reductions in TLR4, IκK and CD11b mRNA were observed. Catalase and hexokinase were increased by obesity, while SOD and G6PDH were decreased. Treatment with GT reduced catalase and increased the GSH/GSSG ratio.
In response to a cafeteria diet, we found a decreased chemotaxis, H2O2 release, MPO activity and HOCl production. We also showed a significant immunomodulatory effect of GT on the obese condition recovering some of these factors such H2O2 and HOCl production, also reducing the levels of inflammatory cytokines.
我们的研究旨在评估自助餐饮食诱导的肥胖是否会改变中性粒细胞的效应/炎症功能,以及绿茶提取物(GT)治疗是否能改善中性粒细胞功能。
雄性Wistar大鼠通过灌胃接受GT治疗(12周/每周5天;500mg/kg体重),并通过自助餐饮食诱导肥胖(8周)。从腹腔获取中性粒细胞(注射牡蛎糖原)。进行了以下分析:吞噬能力、趋化性、髓过氧化物酶活性(MPO)、次氯酸(HOCl)、超氧阴离子(O₂⁻)、过氧化氢(H₂O₂)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNFα)、炎症基因的mRNA水平、钙动员、抗氧化酶、己糖激酶和葡萄糖-6-磷酸脱氢酶(G6PDH)的活性。
肥胖大鼠的中性粒细胞迁移能力、H₂O₂和HOCl生成、MPO活性和O₂⁻生成显著降低。吞噬作用和CD11b mRNA水平升高,而炎症细胞因子释放未改变。Toll样受体4(TLR4)和IκB激酶(IκK)的mRNA水平增强。用GT治疗肥胖大鼠可增加中性粒细胞迁移、MPO活性、H₂O₂、HOCl和O₂⁻生成,而肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)减少(与肥胖大鼠相比)。观察到TLR4、IκK和CD11b mRNA有类似降低。肥胖使过氧化氢酶和己糖激酶增加,而超氧化物歧化酶(SOD)和G6PDH减少。GT治疗降低了过氧化氢酶并增加了谷胱甘肽(GSH)/氧化型谷胱甘肽(GSSG)比值。
对于自助餐饮食,我们发现趋化性、H₂O₂释放、MPO活性和HOCl生成降低。我们还显示GT对肥胖状况有显著的免疫调节作用,恢复了其中一些因素,如H₂O₂和HOCl生成,同时也降低了炎症细胞因子水平。