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1. 兰州市第一人民医院检验科
2. 兰州市第一人民医院病理科
纸质出版日期:2016,
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[1]孙韬,王春霞,李东海,赵谊,曾婷婷.C57BL/6J小鼠急性足肿胀炎症模型的建立及指标评价[J].重庆医科大学学报,2016,41(02):175-178.
Sun Tao, Wang Chunxia, Li Donghai, et al. Establishment and evaluation of acute paw edema inflammation model of C57BL/6J mice[J]. Journal of Chongqing Medical University, 2016,41(2):175-178.
[1]孙韬,王春霞,李东海,赵谊,曾婷婷.C57BL/6J小鼠急性足肿胀炎症模型的建立及指标评价[J].重庆医科大学学报,2016,41(02):175-178. DOI: 10.13406/j.cnki.cyxb.000739.
Sun Tao, Wang Chunxia, Li Donghai, et al. Establishment and evaluation of acute paw edema inflammation model of C57BL/6J mice[J]. Journal of Chongqing Medical University, 2016,41(2):175-178. DOI: 10.13406/j.cnki.cyxb.000739.
目的:建立C57BL/6J小鼠急性足肿胀炎症模型进行模型指标评价。方法:将24只SPF级雄性C57BL/6J小鼠随机分为3组
即正常组、模型组和吲哚美辛对照组。采用角叉菜胶法诱导模型组和吲哚美辛对照组小鼠发病建立急性足肿胀炎症模型。正常组小鼠不做任何处理。各组分别于注射角叉菜胶后1、2、3、4、5、6 h测量足趾厚度
随后处死小鼠取血清标本进行炎性因子检测
取足部组织进行病理学观察。结果:致炎1 h后模型组小鼠足部开始肿胀
2 h后肿胀明显
5 h后达到肿胀高峰。与模型组相比
吲哚美辛对照组则在2 h明显抑制肿胀(P=0.004)
抑制作用持续到6 h(P=0.000)。正常组小鼠无明显变化;模型组较吲哚美辛对照组和正常组小鼠血清肿瘤坏死因子-α(tumour necrosis factor-α
TNF-α)和白介素-1β(interleukin-1β
IL-1β)都明显升高(P=0.000);模型组小鼠足趾病理切片见大量中性粒细胞浸润
吲哚美辛对照组小鼠见少量中性粒细胞浸润
正常组小鼠足部病理未见明显异常。结论:C57BL/6J小鼠急性足肿胀炎症模型方法可靠、可重复性较高以及阳性对照药物吲哚美辛抗足肿胀效果明显
可适用于抗炎药物的常规筛选及评价。足趾厚度改变、血清炎性因子TNF-α和IL-1β升高以及炎症部位病理改变是评价急性足肿胀炎症模型的重要指标。
Objective:To establish and evaluate acute paw edema inflammation model of C57BL/6J mice. Methods:Twenty-four cases of C57BL/6J male mice were randomly divided into 3 groups.The normal group did not receive any treatment;the other two groups were induced to acute inflammation model by carrageenan. The thickness of the paw was measured respec-tively at 1
2
3
4
5
6 hours after the injection of carrageenan.Then the mice were executed
the serum samples were taken for the detection of inflammatory cytokines
and the foot tissue was taken for pathology detection. Results:At 1 h after the inflammation
the paws of mice in model group began to swell. The edema became significant at 2 h after the inflammation. At 5 h after the inflammation
the edema reached the peak. The edema was significantly inhibited in indomathacin group at 2 h after the inflammation
and the inhibition continued till 6 h after the inflammation. The mice in normal group had no significant change. Compared with those in indomathacin group and normal group
the serum TNF-α and IL-1β of mice in normal group were significantly elevated. The pathological sections of paws of mice in model group showed massive infiltration of neutrophils. Little infiltration of neutrophils was seen in mice in indomathacin group. The paw pathology of mice in normal group showed no obvious abnormality. Conclusion:The acute paw edema and inflammation model of C57BL/6J mice is reliable and highly repetitive. The positive controlling drug indomathacin has obvious anti-edema effect. The model is applicable to the routine screening and evaluation of anti-inflammatory drugs. The changes in paw edema
the increase in serum cytokines TNF-α and IL-1β
and the pathological changes in sites of inflammation are very important indicators to evaluate the acute inflammation model.
炎症模型C57BL/6J小鼠足肿胀
inflammation modelC57BL/6J micepaw edema
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