生长激素对大鼠急性坏死性胰腺炎过程中细菌易位的有益作用

Wang Xingpeng, Wang Bingxian, Wu Jianxin, W. Guoliang
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引用次数: 1

摘要

目的:由于肠道细菌易位是急性坏死性胰腺炎(ANP)细菌感染的重要来源之一,而生长激素(GH)具有促进肠上皮细胞增殖的能力,我们在大鼠ANP模型中研究了GH对细菌易位的影响。方法:在大鼠胆管内注射5%牛磺胆酸钠诱导急性坏死性胰腺炎。ANP大鼠分别用人重组生长激素或安慰剂治疗。无ANP诱导的开腹动物(假手术)作为对照。术后24小时抽血进行细菌培养,检测淀粉酶、脂肪酶及内毒素。取腹膜液及肠系膜淋巴结(MLN)、肝脏、胰腺、脾脏标本按标准技术进行细菌培养。通过测量[125I]标记的白蛋白从血液到肠腔的运动来评估肠粘膜通透性。逆转录聚合酶链反应(RT-PCR)检测肝脏和回肠中胰岛素样生长因子-1 (IGF-1) mRNA的表达。胰腺和回肠的形态学变化也进行了分析。结果:GH可显著降低血清淀粉酶和脂肪酶活性,降低血浆内毒素水平,降低细菌易位发生率。同时提高了ANP大鼠的存活率。生长激素治疗可减轻胰腺和回肠炎症的严重程度。与ANP大鼠相比,gh处理大鼠回肠粘膜厚度、绒毛高度和隐窝深度明显增加。与ANP组相比,GH组肠通透性明显降低。GH处理导致回肠IGF-1 mRNA表达上调,而肝脏IGF-1 mRNA表达上调。结论:这些结果表明外源性GH在维持ANP大鼠肠粘膜屏障完整性和减少细菌易位发生率方面具有有益作用。其中一种机制可能是生长激素上调肠道IGF-1 mRNA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Beneficial effects of growth hormone on bacterial translocation during the course of acute necrotizing pancreatitis in rats
OBJECTIVE: Because bacterial translocation from the gut is one of the important sources of bacterial infection in acute necrotizing pancreatitis (ANP), and growth hormone (GH) has the ability to promote intestinal epithelial proliferation, we investigated the effects of GH on bacterial translocation in a rat ANP model. METHODS: Acute necrotizing pancreatitis was induced in rats via injection of 5% sodium taurocholate into the biliopancreatic duct. The rats with ANP were treated with either human recombinant GH or a placebo. Laparotomized animals without ANP induction (sham operation) served as controls. Twenty-four hours after the operation, blood was drawn for bacterial culture and determinations of amylase, lipase and endotoxin. Peritoneal fluid and specimens of mesenteric lymph nodes (MLN), liver, pancreas and spleen were taken for bacterial culture by standard techniques. Intestinal mucosal permeability was assessed by measuring the movement of [125I]-labeled albumin from blood to the intestinal lumen. Insulin-like growth factor-1 (IGF-1) mRNA was detected in the liver and ileum by reverse transcription–polymerase chain reaction (RT-PCR). Morphological changes in the pancreas and ileum were also analyzed. RESULTS: Administration of GH significantly decreased the activity of serum amylase and lipase, decreased the plasma endotoxin level and reduced the incidence of bacterial translocation. Moreover, the survival rate of ANP rats was improved. The severity of inflammation in the pancreas and ileum was reduced by GH treatment. Ileal mucosal thickness, villus height and crypt depth in GH-treated rats were obviously increased as compared with those of ANP rats. The intestinal permeability was markedly decreased in the GH group as compared with the ANP group. GH treatment resulted in upregulation of IGF-1 mRNA expression in ileum, but not in liver. CONCLUSIONS: These results suggest that exogenous GH has beneficial effects in maintaining the integrity of the intestinal mucosal barrier and reducing the incidence of bacterial translocation in rats with ANP. One of the mechanisms might be the upregulation of IGF-1 mRNA in the intestine by GH.
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