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重庆医科大学附属儿童医院新生儿科
纸质出版日期:2009,
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[1]李金纯,韦红,贾盛华,魏小娣.新生儿坏死性小肠结肠炎动物模型建立方法改进与比较[J].重庆医科大学学报,2009,34(03):313-317.
LI Jin-chun, et al. Improvement and comparison of animal models of neonatal necrotizing enterocolitis[J]. Journal of Chongqing Medical University, 2009,34(3):313-317.
目的:在国内外坏死性小肠结肠炎(Necrotizing enterocolitis
NEC)动物模型建立现状基础上提出缺氧复氧冷刺激+LPS灌胃+人工喂养三因素联合造模的新方法(B组)
并与国内外常见的四种方法进行比较。方法:采用出生当日SD新生大鼠为研究对象
按不同造模方式随机分为6组
每组8只。A组大鼠采取人工喂养+缺氧复氧冷刺激
B组大鼠为人工喂养+缺氧复氧冷刺激+LPS灌胃
C组大鼠仅接受缺氧复氧冷刺激
D组大鼠仅接受LPS灌胃
E组为人工喂养组
F为正常对照组。每日定时称量体重
实验结束取肠组织HE染色后观察肠道组织病理损伤情况
采用Nandle评分法对病变程度进行评价。结果:实验过程中
各模型组新生鼠相继出现活动减少
倦怠
进而可见腹胀及大便颜色性状发生改变。实验结束A、B、E组体重下降
C、D、F组体重上升
各组与F组比较有统计差异(P<0.05)。Kruskal-wallis检验发现:体重改变F组>D组>C组>E组>A组>B组。各组病理评分分别为A:3.0±0.53、B:3.63±0.52、C:1.75±0.71、D:1.75±0.46、E:2.38±0.52、F:0.5±0.53
各组与B组比较均有统计差异(P<0.05)。缺氧复氧冷刺激、LPS灌胃、人工喂养均为NEC发病危险因素
三项联合法造模所致肠道病理损伤明显重于其他方法。结论:新生大鼠在缺氧复氧冷刺激+LPS灌胃+人工喂养三因素联合干预下可诱导严重肠道损伤
接近人类新生儿坏死性小肠结肠炎病理改变
可广泛应用于建立新生儿坏死性小肠结肠炎模型。
Objective:To establish a new animal model of neonatal necrotizing enterocolitis (NEC) by cold exposure after hypoxic-reoxygenation treatment
formula feeding and (Lipopolysaccharid
LPS)intragastric administration on the base of the modeling status
and to compare the differences between them. Methods:According to different modeling methods
0-day-postnatal S-D rats were divided into 6 groups randomly
each group including 8 rats. Group A was given cold exposure shortly after hypoxic-reoxygen treatment and received formula feeding. Group B was in the same condition expect extra LPS intragastric administration. Group C was given cold exposure after simple hypoxic-reoxygenation treatment. Group D received LPS intragastric administration. Group E was given formula feeding alone. Group F was set up as control group. All rats were weighed every day and sacrificed on the 4th day. Proximal intestines of ileocecal junction were harvested and were evaluated by HE staining for pathological scoring. Results:All the neonatal rats in model groups had physical inactivity
abdominal distention and a change in stool. On day 3
neonatal rats in group A
B
and E had weight loss
while group C
D
and F had weight gain. The terminal weight and weight change of every model group were different from that of Group F (P<0.05). ByKruskal-wallis analysis
weight changes ofeach group were:Group F>Group D>Group C>Group E> Group A>Group B. The pathological scores (x±s)for each gourp were group A:3.0±0.53
group B:3.63±0.52
group C:1.75±0.71
group D:1.75±0.46
group E:2.38±0.52 and group F 0.5±0.53 respectively. The score of group B had significant differences from those of other 5 groups (P<0.05). Cold exposure after hypoxic-reoxygenation
formula feeding and LPS intragastric administration were all risk factors for NEC. Our newmethod with combination of all these factors could produce the most serious intestine injury. Conclusions:By cold exposure after hypoxic-reoxygenation
formula feeding and LPS intragastric administration
we could produced animal models which had intestine injurysimilar to neonatal necrotizing enterocolitis. This new method could be used for the establishment of NEC animal modle extensively.
新生儿坏死性小肠结肠炎肠道损伤动物模型新方法比较
neonatal necrotizing enterocolitisIntestine injuryAnimal modleNewmethodcomparison
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