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中国龙虾食物变态反应BALB/c鼠模型的建立(英文)
引用本文:陈同强,刘鹏,邱立明,黄菲. 中国龙虾食物变态反应BALB/c鼠模型的建立(英文)[J]. 农业科学与技术, 2013, 0(9): 1291-1294
作者姓名:陈同强  刘鹏  邱立明  黄菲
作者单位:[1]赣南医学院组织胚胎学教研室,江西赣州341000 [2]江西省赣州卫生学校,江西赣州341000 [3]赣南医学院实验动物中心,江西赣州341000
基金项目:Supported by the Science and Technology Project of Department of Education of Jiangxi Province(GJJ08399)~~
摘    要:[目的]通过腹腔注射的致敏方式建立中国龙虾食物变态反应Balb/c小鼠模型,探讨中国龙虾食物变态反应体外鉴定与评价方法。[方法]将40只雄性Balb/c小鼠分为卵清蛋白(OVA)阳性对照组、Coca’s液阴性对照组、空白对照组和模型组,以OVA、中国龙虾粗提蛋白,加氢氧化铝佐剂腹腔注射免疫Balb/c小鼠,建立食物变态反应小鼠模型。ELISA法测定第二次致敏激发后血清中IgE与组胺水平并进行被动皮肤过敏试验(PCA)确定特异性IgE抗体滴度,同时观察脾指数、小肠组织学变化及激发后的食物变态反应症状。[结果]末次激发后1 h采血,中国龙虾粗提蛋白组血清IgE含量为236.75(±73.39)μg/L,与阳性对照OVA组无区别,与阴性对照Coca’s液组和正常对照组相比显著升高(P〈0.01);中国龙虾粗提蛋白组的组胺含量406.55(±232.79)μg/L与正常对照组相比显著升高(P〈0.01);PCA反应中国龙虾粗提蛋白组血清特异性IgE抗体滴度达到1/16;中国龙虾粗提蛋白组和OVA致敏组小鼠脾指数明显大于Coca’s液或正常对照组(P〈0.01)且前两组小肠粘膜固有层皆出现淋巴细胞、嗜酸性粒细胞等炎性细胞浸润。[结论]建立了一种中国龙虾食物变态反应小鼠模型,通过ELISA测定血清IgE和组胺以及PCA确定特异性IgE抗体滴度可作为一种鉴定与评价中国龙虾食物变态反应的方法。

关 键 词:中国龙虾  Balb  c鼠  食物变态反应

Establishment of BALB/c Mice Model for Food Allergy to Chinese Lobsters
Tongqiang CHEN;Peng LIU;Liming QIU;Fei HUANG. Establishment of BALB/c Mice Model for Food Allergy to Chinese Lobsters[J]. Agricultural Science & Technology, 2013, 0(9): 1291-1294
Authors:Tongqiang CHEN  Peng LIU  Liming QIU  Fei HUANG
Affiliation:Tongqiang CHEN;Peng LIU;Liming QIU;Fei HUANG;Teaching and Research Office of Histology and Embryology,Gannan Medical College;Health School of Ganzhou in Jiangxi Province;Laboratory Animal Center,Gannan Medical College;
Abstract:[Objective] This study aimed to establish Balb/c mice model for food allergy caused by Chinese lobsters through using intraperitoneal injection for sensitization and explore methods for in vitro identification and evaluation of food allergy caused by Chinese lobsters. [Method] The 40 male Bal/c mice were divided into ovalbumin(OVA) positive control group, Coca's solution negative control group, blank control group and model group. Balb/c mice model was established by intraperitoneally injection of immunized Balb/c mice with OVA or Chinese lobster crude protein with aluminum hydroxide adjuvant. IgE and histamine levels in serum after the second challenge were determined by ELISA method, and the specific IgE antibody titer was determined by passive cutaneous anaphylaxis test(PCA); additionally, spleen index and histological changes in the small intestine, as well as food allergy symptoms after challenge were also calculated or observed. [Results] After the last challenge, IgE content was(236.75 ±73.39) μg/L in the Chinese lobster crude protein group, revealing no difference with that in the OVA group, but significantly higher than that in either the Coca's solution group or the blank control group(P 0.01);histamine content in serum in the Chinese lobster crude protein group was(406.55±232.79), significantly higher than that in the blank control group(P0.01). In the passive cutaneous anaphylaxis test, IgE antibody titer reached 1/16 after the last challenge in the Chinese lobster crude protein group. Spleen index in both Chinese lobster crude protein group and OVA group was significantly greater than that in either the Coca's solution group or the blank control group(P0.01). What's more, infiltration of inflammatory cells like lymphocytes and eosnophils at the lamina propria of intestinal mucosa was also observed both Chinese lobster crude protein group and OVA group. [Conclusion] This study established Balb/c mice model for food allergy caused by Chinese lobsters; serum IgE and ELISA assay and specific IgE antibody titer in PCA test can be used for the in vitro identification and evaluation of food allergies caused by Chinese lobsters.
Keywords:Chinese lobsters  Balb/c mice  Food allergies
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