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首页> 外文期刊>Journal of Nutrition >Cow Milk Allergy Symptoms Are Reduced in Mice Fed Dietary Synbiotics during Oral Sensitization with Whey
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Cow Milk Allergy Symptoms Are Reduced in Mice Fed Dietary Synbiotics during Oral Sensitization with Whey

机译:在乳清口服增敏过程中,小鼠喂养的饮食合生素减少了牛奶过敏症状

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摘要

Cow milk allergy is the most common food allergy in children. So far, no effective treatment is available to prevent or cure food allergy. The purpose of this study was to compare effects of dietary supplementation with a prebiotic mixture (Immunofortis), a probiotic strain [Bifidobacterium breve M-16V], or a synbiotic diet combining both on the outcome of the allergic response when provided during oral sensitization with whey in mice. Mice were fed diets containing 2% (wt:wt) Immunofortis and/or the B. breve M-16V (n = 6/group). The acute allergic skin response was determined by measuring ear swelling. Antigen-induced anaphylaxis was scored. Furthermore, whey-specific serum immunoglobulins and mouse mast cell protease-1 (mMCP-1) were determined. In mice fed the synbiotic mixture, the allergic skin response and the anaphylactic reaction were strongly reduced compared with whey-sensitized mice fed the control diet (P < 0.01). Immunofortis or B. breve M-16V alone were significantly less effective in reducing the allergic skin response than the synbiotic diet and did not reduce the anaphylactic reaction. The whey-specific IgE and IgG1 responses were not affected; however, IgG2a was greater in all treated groups than in the control group (P sup> 0.05). Serum mMCP-1 concentrations, reflecting mucosal mast cell degranulation, were lower in mice fed synbiotics compared with those fed the control diet (P < 0.01). Dietary supplementation with Immunofortis, B. breve M-16V, and particularly the synbiotic mixture, provided during sensitization, reduces the allergic effector response in a murine model of IgE-mediated hypersensitivity that mimics the human route of sensitization. This model shows the potential for dietary intervention with synbiotics in reducing the allergic response to food allergens.
机译:牛奶过敏是儿童中最常见的食物过敏。 到目前为止,尚无有效的方法来预防或治愈 食物过敏。这项研究的目的是比较益生菌混合物(Immunofortis),益生菌菌株[短双歧杆菌M-16V]或合生素 饮食结合在小鼠乳清口服致敏过程中提供的过敏反应结果 。给小鼠 喂食含2%(wt:wt)免疫福特和/或 B的饮食。短M-16V(n = 6 /组)。急性过敏性皮肤反应 是通过测量耳肿胀来确定的。对抗原引起的过敏反应 进行评分。此外,测定了乳清特异性血清免疫球蛋白和小鼠肥大细胞蛋白酶-1(mMCP-1)。在 饲喂该合生素混合物的小鼠中,与 乳清致敏小鼠饲喂对照饮食相比,其皮肤过敏反应和 过敏反应明显降低( P <0.01)。单独的Imfortofortis或B. breve M-16V在减少过敏性皮肤反应方面的功效明显低于合生素饮食,并且没有减少过敏反应反应。乳清特异性 IgE和IgG 1 反应不受影响;然而,所有治疗组的IgG 2a 都比对照组大(P sup> 0.05)。饲喂合生素的小鼠的血清mMCP-1浓度反映了粘膜肥大细胞的脱颗粒,与饲喂对照饮食的小鼠相比更低(P <0.01)。在致敏过程中提供的Immunofortis,短双歧杆菌M-16V的膳食补充剂 ,尤其是合生元 混合物,可降低过敏性动物的模仿人类致敏途径的IgE介导的超敏反应 的小鼠模型。该模型显示了 用合生素进行饮食干预的潜力,可以减少 对食物过敏原的过敏反应。

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  • 来源
    《Journal of Nutrition》 |2009年第7期|1398-1403|共6页
  • 作者单位

    Pharmaceutical Sciences, Pharmacology and Pathophysiology, Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Utrecht 3584 CA, The Netherlands and;

    Pharmaceutical Sciences, Pharmacology and Pathophysiology, Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Utrecht 3584 CA, The Netherlands and|Danone Research–Centre for Specialised Nutrition, Wageningen 6704 PH, The Netherlands;

    Pharmaceutical Sciences, Pharmacology and Pathophysiology, Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Utrecht 3584 CA, The Netherlands and;

    Danone Research–Centre for Specialised Nutrition, Wageningen 6704 PH, The Netherlands;

    Danone Research–Centre for Specialised Nutrition, Wageningen 6704 PH, The Netherlands;

    Danone Research–Centre for Specialised Nutrition, Wageningen 6704 PH, The Netherlands;

    Pharmaceutical Sciences, Pharmacology and Pathophysiology, Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Utrecht 3584 CA, The Netherlands and|Danone Research–Centre for Specialised Nutrition, Wageningen 6704 PH, The Netherlands;

    Pharmaceutical Sciences, Pharmacology and Pathophysiology, Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Utrecht 3584 CA, The Netherlands and;

    Pharmaceutical Sciences, Pharmacology and Pathophysiology, Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Utrecht 3584 CA, The Netherlands and|Danone Research–Centre for Specialised Nutrition, Wageningen 6704 PH, The Netherlands;

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