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首页> 外文期刊>American Journal of Physiology >Animal models of gastrointestinal and liver diseases. Animal models of necrotizing enterocolitis: pathophysiology, translational relevance, and challenges
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Animal models of gastrointestinal and liver diseases. Animal models of necrotizing enterocolitis: pathophysiology, translational relevance, and challenges

机译:胃肠道和肝脏疾病的动物模型。坏死性小肠结肠炎的动物模型:病理生理,翻译相关性和挑战

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摘要

Necrotizing enterocolitis is the leading cause of morbidity and mortality from gastrointestinal disease in premature infants and is characterized by initial feeding intolerance and abdominal distention followed by the rapid progression to coagulation necrosis of the intestine and death in many cases. Although the risk factors for NEC development remain well accepted, namely premature birth and formula feeding, the underlying mechanisms remain incompletely understood. Current thinking indicates that NEC develops in response to an abnormal interaction between the mucosal immune system of the premature host and an abnormal indigenous microflora, leading to an exaggerated mucosal inflammatory response and impaired mesenteric perfusion. In seeking to understand the molecular and cellular events leading to NEC, various animal models have been developed. However, the large number and variability between the available animal models and the unique characteristics of each has raised important questions regarding the validity of particular models for NEC research. In an attempt to provide some guidance to the growing community of NEC researchers, we now seek to review the key features of the major NEC models that have been developed in mammalian and nonmammalian species and to assess the advantages, disadvantage, challenges and major scientific discoveries yielded by each. A strategy for model validation is proposed, the principal models are compared, and future directions and challenges within the field of NEC research are explored.
机译:坏死性小肠结肠炎是早产儿胃肠道疾病的发病率和死亡率的主要原因,其特征是最初的喂养不耐受和腹胀,随后在许多情况下迅速发展为肠凝血性坏死并死亡。尽管NEC发展的风险因素仍然被人们所接受,即早产和配方奶喂养,但其潜在机制仍不完全清楚。当前的想法表明,NEC是由于早产宿主的粘膜免疫系统与异常的本地菌群之间的相互作用异常而发展的,从而导致粘膜炎性反应过度和肠系膜灌注受损。为了寻求理解导致NEC的分子和细胞事件,已经开发了各种动物模型。但是,可用的动物模型之间的数量众多且差异很大,每种动物模型的独特特征也引发了有关NEC研究特定模型有效性的重要问题。为了为不断增长的NEC研究者社区提供一些指导,我们现在寻求回顾在哺乳动物和非哺乳动物物种中开发的主要NEC模型的关键特征,并评估其优势,劣势,挑战和重大科学发现各自屈服。提出了一种模型验证策略,比较了主要模型,并探索了NEC研究领域内的未来方向和挑战。

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