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Caffeic acid phenethyl ester attenuates allergic airway inflammation and hyperresponsiveness in murine model of ovalbumin-induced asthma

机译:咖啡酸苯乙酯减轻卵清蛋白诱导哮喘小鼠模型的过敏性气道炎症和反应过度

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摘要

Caffeic acid phenethyl ester (CAPE) is a biologically active ingredient of propolis, which has several interesting biological properties, including antioxidant and anti-inflammatory; however, its anti-allergic effects are poorly understood. The objective of this study was to determine whether treatment with CAPE results in significant inhibition of asthmatic reactions in a mouse model. Mice sensitized and challenged with ovalbumin (OVA) had the following typical asthmatic reactions: an increase in the number of eosinophils in bronchoalveolar lavage (BAL) fluid; a marked influx of inflammatory cells into the lung around blood vessels and airways, and airway luminal narrowing; the development of airway hyperresponsiveness (AHR); the presence of tumor necrosis factor-alpha (TNF-alpha) and Th2 cytokines, including IL-4 and IL-5, in the BAL fluid; and the presence of allergen-specific IgE in the serum. Five successive intraperitoneal administrations of CAPE before the last airway OVA challenge resulted in significant inhibition of characteristic asthmatic reactions. We determined that increased generation of reactive oxygen species (ROS) by inhalation of OVA was diminished via the administration of CAPE in BAL fluid, as well as nuclear factor-kappa B (NF-kappa B) DNA binding activity. These findings indicate that oxidative stress may have a crucial function in the pathogenesis of bronchial asthma, and that CAPE may be useful as an adjuvant therapy for the treatment of bronchial asthma. (c) 2008 Elsevier Inc. All rights reserved.
机译:咖啡酸苯乙酯(CAPE)是蜂胶的生物活性成分,具有多种有趣的生物学特性,包括抗氧化剂和抗炎剂;然而,其抗过敏作用知之甚少。这项研究的目的是确定用CAPE治疗是否能在小鼠模型中显着抑制哮喘反应。卵清蛋白(OVA)致敏和攻击的小鼠出现以下典型的哮喘反应:支气管肺泡灌洗液(BAL)中嗜酸性粒细胞数量增加;炎性细胞大量流入血管和气道周围的肺部,气道腔狭窄。气道高反应性(AHR)的发展; BAL液中是否存在肿瘤坏死因子-α(TNF-α)和Th2细胞因子,包括IL-4和IL-5;以及血清中过敏原特异性IgE的存在。在最后一次气道OVA刺激之前,连续五次腹膜内给予CAPE可显着抑制特征性哮喘反应。我们确定,通过在BAL液中施用CAPE以及核因子-κB(NF-κB)DNA结合活性,减少了通过吸入OVA产生的活性氧(ROS)的增加。这些发现表明,氧化应激可能在支气管哮喘的发病机理中起着至关重要的作用,并且CAPE可用作治疗支气管哮喘的辅助疗法。 (c)2008 Elsevier Inc.保留所有权利。

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