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首页> 外文期刊>Nutrition Research >Mice with infectious colitis exhibit linear growth failure and subsequent catch-up growth related to systemic inflammation and IGF-1
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Mice with infectious colitis exhibit linear growth failure and subsequent catch-up growth related to systemic inflammation and IGF-1

机译:具有传染性结肠炎的小鼠表现出线性生长衰竭和随后与全身炎症和IGF-1相关的追赶生长

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In developing communities, intestinal infection is associated with poor weight gain and linear-growth failure. Prior translational animal models have focused on weight gain investigations into key contributors to linear growth failure have been lacking. We hypothesized that murine intestinal infection with Citrobacter rodentium would induce linear-growth failure associated with systemic inflammation and suppressed serum levels of insulin-like growth factor-1 (IGF-1). We evaluated 4 groups of mice infected or sham infected on day-of-life 28: uninfected-controls, wild-type C rodentium-infected, partially attenuated C rodentium-infected (with deletion of 3 serine protease genes involved in colonization), and pair-fed (given the amount of daily food consumed by the wild-type C rodentium group). Relative to the uninfected group, mice infected with wild-type C rodentium exhibited temporal associations of lower food intake, weight loss, linear-growth failure, higher IL-6 and TNF-alpha and lower IGF-1. However, relative to the pair-fed group, the C rodentium-infected group only differed significantly by linear growth and systemic inflammatory cytokines. Between post-infection days 15-20, the infected group exhibited resolution of systemic inflammation. Between days 16-20, both wild-type C rodentium and pair-fed groups exhibited rapid linear-growth velocities exceeding the uninfected and mutant C rodentium groups; during this time levels of IGF-1 increased to match the uninfected group. We submit this as a model providing important opportunities to study mechanisms of catch-up growth related to intestinal inflammation. We conclude that in addition to known effects of weight loss, infection with C rodentium induces linear-growth failure potentially related to systemic inflammation and low levels of IGF-1, with catch-up of linear growth following resolution of inflammation. (C) 2017 Elsevier Inc. All rights reserved.
机译:在开发社区中,肠道感染与重量增长和线性生长衰竭不良有关。先前的平移动物模型的重点是重量增益调查转为关键贡献者对线性生长失败的贡献缺乏。我们假设小鼠肠道感染与柠檬酸杆菌毒素感染会诱导与全身炎症相关的线性生长失败,并抑制胰岛素样生长因子-1(IGF-1)的血清水平。我们评估了4组感染或虚假的小鼠感染的小鼠28:未感染的对照,野生型C鼠疫感染,部分减毒的C鼠笼(缺失参与殖民化的3个丝氨酸蛋白酶基因),和对喂养(鉴于野生型C鼠李群组消耗的日常食物量)。相对于未感染的组,用野生型C鼠感染的小鼠表现出较低食物摄入,减肥,线性生长衰竭,较高IL-6和TNF-α和下IGF-1的时间关联。然而,相对于对喂养的组,C鼠李毒素感染的组仅通过线性生长和全身炎性细胞因子显着差异。在感染后15-20天之间,感染的群体表现出全身炎症的决定。在第16-20天之间,野生型C鼠李和配对组两者都表现出快速的线性生长速度超过未感染和突变的C鼠李群;在此期间,IGF-1的水平增加以匹配未感染的组。我们将其作为一种模型,为肠炎相关的追赶增长机制提供了重要机会。我们得出结论,除了重量损失的已知效果之外,C鼠李的感染均导致与全身炎症和低水平的IGF-1有关的线性生长衰竭,随着炎症分辨率的线性生长追赶。 (c)2017年Elsevier Inc.保留所有权利。

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