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大鼠肠缺血-再灌注损伤后细菌易位发生部位的实验研究 被引量:3

The site of bacterial translocation after rat intestinal ischemia-reperfusion
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摘要 目的:探讨肠道缺血-再灌注损伤对不同肠段细菌易位的影响。方法:将大鼠随机分为对照组(行假手术)和肠道缺血-再灌注组(分别于再灌注后1、6和24 h取材)。检测空肠、回肠和结肠的细菌、内毒素易位情况,各段肠系膜静脉中的肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)水平。结果:对照组和肠道缺血-再灌注1 h组各肠段系膜淋巴结细菌培养均阴性,再灌注后24 h组空肠、回肠系膜淋巴结细菌易位率明显高于对照组和结肠系膜淋巴结(P<0.05);两组大鼠各段肠系膜静脉血培养、内毒素测定均为阴性;肠道缺血-再灌注后1 h和6 h组大鼠TNF-α浓度明显高于对照组(P<0.05);各段肠系膜静脉血IL-6浓度均明显高于对照组(P<0.05),再灌注后6 h组,空肠、回肠的肠系膜静脉血IL-6浓度明显高于结肠(P<0.05)。结论:肠道缺血-再灌注损伤可造成肠道细菌易位,空、回肠更易遭受肠缺血-再灌注损伤的打击,从而发生细菌易位。 Objective: The study was designed to find out the effect of intestinal ischemia and reperfusion injury on gut barrier function and the site of bacterial translocation.Methods: Healthy male SPF SD rats were divided into two groups at random: group A[simple laparotomy(sham),known as the control group] and group B[intestinal ischemia and reperfusion(I/R)].Bacterial translocation and the levels of endotoxin and cytokine in mesenteric circulation were measured separately in jejunum,ileum and colon and at 1,6 and 24 hours after I/R.Results: There was no bacteria in all groups in the mesenteric lymph nodes(MLN) at 1h after reperfusion.Colony counts of jejunum and ileum MLN in 24 h after reperfusion I/R in group B were significantly higher than that of colon MLN(P〈0.05).No bacteria and endotoxin were detected in the blood from the mesenteric vein in all groups.Concentrations of cytokine TNF-α and IL-6 at 1,6 h after reperfusion in the I/R in group B was significantly higher than that in sham group(P〈0.05).The concentration of IL-6 in mesenteric vein blood of jejunum and ileum was significantly higher than that of colon at 6h after reperfusion in the I/R group(P〈0.05). Conclusion: Bacterial translocation can be caused by Intestinal I/R.Compared with the large intestine,the small intestine is easier to injury of intestinal I/R.
出处 《肠外与肠内营养》 CAS 北大核心 2010年第4期239-242,共4页 Parenteral & Enteral Nutrition
基金 国家自然科学基金重点项目(30830098)
关键词 肠缺血-再灌注损伤 细菌易位 炎症因子 大鼠 Intestinal ischemia/reperfusion Bacterial translocation Cytokine Rat
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