Peh Hong Yong, Ho Wanxing Eugene, Cheng Chang, Chan Tze Khee, Seow Ann Ching Genevieve, Lim Albert Y H, Fong Chee Wai, Seng Kok Yong, Ong Choon Nam, Wong W S Fred
Department of Pharmacology, Yong Loo Lin School of Medicine, National University Health System, Singapore 119228; Immunology Program, Life Science Institute, National University of Singapore, Singapore 117456;
Saw Swee Hock School of Public Health, National University Health System, Singapore 117597; Singapore-MIT Alliance for Research and Technology, National University of Singapore, Singapore 117543;
J Immunol. 2015 Jul 15;195(2):437-44. doi: 10.4049/jimmunol.1500362. Epub 2015 Jun 3.
Inflammation and oxidative damage contribute to the pathogenesis of asthma. Although corticosteroid is the first-line treatment for asthma, a subset of patients is steroid resistant, and chronic steroid use causes side effects. Because vitamin E isoform γ-tocotrienol possesses both antioxidative and anti-inflammatory properties, we sought to determine protective effects of γ-tocotrienol in a house dust mite (HDM) experimental asthma model. BALB/c mice were sensitized and challenged with HDM. Bronchoalveolar lavage (BAL) fluid was assessed for total and differential cell counts, oxidative damage biomarkers, and cytokine levels. Lungs were examined for cell infiltration and mucus hypersecretion, as well as the expression of antioxidants and proinflammatory biomarkers. Sera were assayed for IgE and γ-tocotrienol levels. Airway hyperresponsiveness in response to methacholine was measured. γ-Tocotrienol displayed better free radical-neutralizing activity in vitro and inhibition of BAL fluid total, eosinophil, and neutrophil counts in HDM mouse asthma in vivo, as compared with other vitamin E isoforms, including α-tocopherol. Besides, γ-tocotrienol abated HDM-induced elevation of BAL fluid cytokine and chemokine levels, total reactive oxygen species and oxidative damage biomarker levels, and of serum IgE levels, but it promoted lung-endogenous antioxidant activities. Mechanistically, γ-tocotrienol was found to block nuclear NF-κB level and enhance nuclear Nrf2 levels in lung lysates to greater extents than did α-tocopherol and prednisolone. More importantly, γ-tocotrienol markedly suppressed methacholine-induced airway hyperresponsiveness in experimental asthma. To our knowledge, we have shown for the first time the protective actions of vitamin E isoform γ-tocotrienol in allergic asthma.
炎症和氧化损伤在哮喘发病机制中起作用。尽管皮质类固醇是哮喘的一线治疗药物,但一部分患者对类固醇耐药,且长期使用类固醇会产生副作用。由于维生素E异构体γ-生育三烯酚具有抗氧化和抗炎特性,我们试图确定γ-生育三烯酚在屋尘螨(HDM)实验性哮喘模型中的保护作用。用HDM对BALB/c小鼠进行致敏和激发。评估支气管肺泡灌洗(BAL)液中的总细胞计数和分类细胞计数、氧化损伤生物标志物及细胞因子水平。检查肺组织的细胞浸润和黏液高分泌情况,以及抗氧化剂和促炎生物标志物的表达。检测血清中的IgE和γ-生育三烯酚水平。测量对乙酰甲胆碱的气道高反应性。与其他维生素E异构体(包括α-生育酚)相比,γ-生育三烯酚在体外表现出更好的自由基中和活性,并且在体内HDM小鼠哮喘模型中能抑制BAL液中的总细胞、嗜酸性粒细胞和中性粒细胞计数。此外,γ-生育三烯酚可减轻HDM诱导的BAL液细胞因子和趋化因子水平、总活性氧和氧化损伤生物标志物水平以及血清IgE水平的升高,但它能促进肺内源性抗氧化活性。从机制上讲,发现γ-生育三烯酚比α-生育酚和泼尼松龙更能在更大程度上阻断肺裂解物中的核NF-κB水平并提高核Nrf2水平。更重要的是,γ-生育三烯酚在实验性哮喘中显著抑制乙酰甲胆碱诱导的气道高反应性。据我们所知,我们首次展示了维生素E异构体γ-生育三烯酚在过敏性哮喘中的保护作用。