Chen Jie, Wang Xing-Peng, Liu Pi, Wu Ka, Xu Min, Yu Xiao-Feng, Wang Gen-Sheng
Department of Gastroenterology, First People's Hospital of Shanghai, Jiaotong University, Shanghai 200080, China.
Zhonghua Yi Xue Za Zhi. 2004 Oct 17;84(20):1726-31.
To evaluate the effects of continuous early enteral nutrition on the gut barrier function in acute necrotizing pancreatitis (ANP).
Thirty mongrel dogs underwent laparotomy and 5% mixed solution of sodium taurocholate with trypsin was infused into the pancreatic ducts so as to induce model of ANP. Permanent duodenal and jejunal fistulas were retained. Then the 30 dogs were randomly divided into 6 groups of 5 dogs: total parenteral nutrition (TPN) group, normal saline (NS) group, duodenal nutrison multifibre (DN) group, duodenal PEPTI-2000Varient (DP) group, jejunal nutrison multifibre (JN) group, and jejunal PEPTI-2000Varient (JP) group, the last 4 groups being called enteral nutrition (EN) group together. Infusion of nutritional solutions was performed via the duodenal or jejunal fistulas, beginning 24 hours after the operation and lasting for 5 days. The levels of endotoxin and D-(-)-lactate in the peripheral plasma were measured every day. On the days 2 and 5 after the operation test solution to measure the enteral permeability, containing lactulose and mannitol, was infused via the fistulas and then urine within 6 hours thereafter was collected to detect the concentrations of lactulose and mannitol and calculate the lactulose/mannitol ratio. Seven days after the operation the dogs were killed to take the pancreas and intestines to be examined by microscopy. Feces was collected. ERIC-PCR fingerprint method was used to examine the structure and distribution of ERIC series of the microbial communities in the gut.
The plasma D-(-)-lactate of the NS group gradually increased and peaked on the 5th day after the operation, and that of the TPN group gradually increased too, however, lower than that of the NS group at any time points and was significantly lower on the 5th day (P < 0.05). The plasma D-(-)-lactate of the EN groups increased first and then decreased and was lower than those of the TPN and NS groups with significant differences on the 4th and 5th days (all P < 0.05). Five days after the operation the lactulose/mannitol ratio decreased in every groups and with significant differences between the EN groups and TPN and NS groups and between the TPN and NS groups (all P < 0.05). The plasma endotoxin level increased in every groups, however, the endotoxin levels of the EN groups at any time points were all lower than those of the TPN group and much more lower than those in the NS group with significant differences between the EN groups and TPN group and NS group on specific days after operation (all P < 0.05). The pathological changes of the intestinal mucosa were more severe in the NS group than in the TPN group, and much more severe than in the EN groups. The makeup and distribution of intestinal microbial in the EN groups were similar to those of the normal dogs. However, the makeup and distribution of intestinal microbial in the TPN groups were quite different from those of the normal dogs.
EN helps maintain gut mucosal barrier, decreases endotoxin translocation, and decreases the extent of mucosal atrophy in ANP.
评估早期持续肠内营养对急性坏死性胰腺炎(ANP)肠道屏障功能的影响。
30只杂种犬行剖腹术,将5%牛磺胆酸钠与胰蛋白酶混合液注入胰管以诱导ANP模型,保留永久性十二指肠和空肠瘘。然后将30只犬随机分为6组,每组5只:全胃肠外营养(TPN)组、生理盐水(NS)组、十二指肠能全力(DN)组、十二指肠百普力(DP)组、空肠能全力(JN)组和空肠百普力(JP)组,后4组统称为肠内营养(EN)组。术后24小时开始经十二指肠或空肠瘘输注营养溶液,持续5天。每天测定外周血浆中内毒素和D-(-)-乳酸水平。术后第2天和第5天,经瘘管输注含乳果糖和甘露醇的肠通透性测试溶液,然后收集此后6小时内的尿液,检测乳果糖和甘露醇浓度并计算乳果糖/甘露醇比值。术后7天处死犬,取胰腺和肠道进行显微镜检查。收集粪便。采用ERIC-PCR指纹法检测肠道微生物群落ERIC系列的结构和分布。
NS组血浆D-(-)-乳酸逐渐升高,术后第5天达峰值,TPN组血浆D-(-)-乳酸也逐渐升高,但在任何时间点均低于NS组,且在第5天显著低于NS组(P<0.05)。EN组血浆D-(-)-乳酸先升高后降低,在第4天和第5天低于TPN组和NS组,差异有统计学意义(均P<0.05)。术后5天,各组乳果糖/甘露醇比值均降低,EN组与TPN组和NS组之间以及TPN组和NS组之间差异有统计学意义(均P<0.05)。各组血浆内毒素水平均升高,但EN组在任何时间点的内毒素水平均低于TPN组,且远低于NS组,术后特定天数EN组与TPN组和NS组之间差异有统计学意义(均P<0.05)。NS组肠黏膜病理改变比TPN组更严重,比EN组更严重得多。EN组肠道微生物的组成和分布与正常犬相似。然而,TPN组肠道微生物的组成和分布与正常犬有很大不同。
EN有助于维持肠道黏膜屏障,减少内毒素移位,减轻ANP时黏膜萎缩程度。