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Assessment of the sensitizing potential of processed peanut proteins in Brown Norway rats: roasting does not enhance allergenicity

机译:评估挪威褐大鼠中加工的花生蛋白的致敏潜力:烘烤不会增强变应原性

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摘要

Background: IgE-binding of process-modified foods or proteins is the most common method for examination of how food processing affects allergenicity of food allergens. How processing affects sensitization capacity is generally studied by administration of purified food proteins or food extracts and not allergens present in their natural food matrix. [br/]Objectives: The aim was to investigate if thermal processing increases sensitization potential of whole peanuts via the oral route. In parallel, the effect of heating on sensitization potential of the major peanut allergen Ara h 1 was assessed via the intraperitoneal route. Methods: Sensitization potential of processed peanut products and Ara h 1 was examined in Brown Norway (BN) rats by oral administration of blanched or oil-roasted peanuts or peanut butter or by intraperitoneal immunization of purified native (N-), heated (H-) or heat glycated (G-) Ara h 1. Levels of specific IgG and IgE were determined by ELISA and IgE functionality was examined by rat basophilic leukemia (RBL) cell assay. [br/]Results: In rats dosed orally, roasted peanuts induced significant higher levels of specific IgE to NAra h 1 and 2 than blanched peanuts or peanut butter but with the lowest level of RBL degranulation. However, extract from roasted peanuts was found to be a superior elicitor of RBL degranulation. Process-modified Ara h 1 had similar sensitizing capacity as NAra h 1 but specific IgE reacted more readily with process-modified Ara h 1 than with native. [br/]Conclusions: Peanut products induce functional specific IgE when dosed orally to BN rats. Roasted peanuts do not have a higher sensitizing capacity than blanched peanuts. In spite of this, extract from roasted peanuts is a superior elicitor of RBL cell degranulation irrespectively of the peanut product used for sensitization. The results also suggest that new epitopes are formed or disclosed by heating Ara h 1 without glucose.
机译:背景:经过工艺修饰的食品或蛋白质的IgE结合是检查食品加工如何影响食品过敏原致敏性的最常用方法。通常通过施用纯化的食物蛋白或食物提取物而不是天然食物基质中存在的过敏原来研究加工如何影响致敏能力。 [br /]目的:目的是研究热处理是否通过口服途径增加了整个花生的致敏性。同时,通过腹膜内途径评估了加热对主要花生过敏原Ara h 1致敏性的影响。方法:通过口服变白或油烘烤的花生或花生酱,或通过腹膜内免疫纯化的天然(N-),加热(H-),在褐挪威(BN)大鼠中检查加工后的花生产品和Ara h 1的致敏潜力。 )或热糖化(G-)Ara h 1.通过ELISA确定特异性IgG和IgE的水平,并通过大鼠嗜碱性白血病(RBL)细胞测定法检查IgE功能。 [br /]结果:在口服给药的大鼠中,烤花生诱导的NAra h 1和2特异性IgE水平明显高于脱皮的花生或花生酱,但RBL脱粒水平最低。但是,发现从烤花生中提取的提取物是RBL脱粒的上等引发剂。过程修饰的Ara h 1具有与NAra h 1相似的敏化能力,但特定IgE与过程修饰的Ara h 1相比,与天然IgE的反应更容易。结论:花生产品口服给BN大鼠时会诱导功能特异性IgE。烤花生没有比漂白花生更高的敏化能力。尽管如此,与用于敏化的花生产品无关,来自烤花生的提取物是RBL细胞脱粒的优良引发剂。结果还表明,通过加热不含葡萄糖的Ara h 1形成或公开了新的表位。

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