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一种用于研究脓毒症长期分解代谢状态的持续性大鼠模型。

A sustained rat model for studying the long-lasting catabolic state of sepsis.

作者信息

Breuille D, Voisin L, Contrepois M, Arnal M, Rose F, Obled C

机构信息

Clintec Technologies, 78140 Vélizy-Villacoublay, INRA Theix, 63122 Ceyrat, France.

出版信息

Infect Immun. 1999 Mar;67(3):1079-85. doi: 10.1128/IAI.67.3.1079-1085.1999.

Abstract

Most animal models of sepsis induced high mortality or early recovery and do not mimic the long-lasting catabolic state observed in patients. The purpose of this study is to develop a model of sepsis which reproduces these disorders, especially the long-lasting muscle wasting. This report summarizes our observations in a series of seven experiments using this model with rats to study the route of live Escherichia coli administration, dose of bacteria, reproducibility of the model, bacterial count in tissues, comparison of injection of live or dead bacteria, metabolic perturbations linked to infection, and potential role of tumor necrosis factor alpha (TNF-alpha) in muscle wasting. After intravenous infection, animals were anorexic and the catabolic state was long-lasting: body weight loss for 2 to 3 days followed by a chronic wasting state for several days. Liver, spleen, lung protein content, and plasma concentration of alpha2-macroglobulin were increased 2 and 6 days after infection. At 6 days, muscle protein content was substantially (-40%) reduced. The plasma TNF-alpha level measured 1.5 h after infection correlated with body weight loss observed 9 days later. The inhibition of TNF-alpha secretion by administration of pentoxifylline 1 h before infection reduced muscle wasting and activation of proteolysis at day 2 and abolished them at day 6. This septic model mimics in rats the prolonged protein metabolism alterations and muscle atrophy characteristics of infected patients and thus is useful for studying the impact of nutritional support on outcome.

摘要

大多数脓毒症动物模型会导致高死亡率或早期恢复,无法模拟患者中观察到的长期分解代谢状态。本研究的目的是建立一种脓毒症模型,该模型能够再现这些紊乱情况,尤其是长期的肌肉消耗。本报告总结了我们在一系列七项实验中的观察结果,这些实验使用该模型对大鼠进行研究,以探讨活大肠杆菌的给药途径、细菌剂量、模型的可重复性、组织中的细菌计数、活细菌与死细菌注射的比较、与感染相关的代谢紊乱,以及肿瘤坏死因子α(TNF-α)在肌肉消耗中的潜在作用。静脉感染后,动物出现厌食,分解代谢状态持续时间长:体重在2至3天内下降,随后在数天内处于慢性消耗状态。感染后2天和6天,肝脏、脾脏、肺的蛋白质含量以及α2-巨球蛋白的血浆浓度升高。在第6天,肌肉蛋白质含量大幅降低(-40%)。感染后1.5小时测得的血浆TNF-α水平与9天后观察到的体重减轻相关。在感染前1小时给予己酮可可碱抑制TNF-α分泌,可减少第2天的肌肉消耗和蛋白水解激活,并在第6天时消除这些现象。这种脓毒症模型在大鼠中模拟了感染患者长期的蛋白质代谢改变和肌肉萎缩特征,因此对于研究营养支持对预后的影响很有用。

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