Department of Surgery, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania;
Division of Newborn Medicine, Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Am J Physiol Gastrointest Liver Physiol. 2014 Jun 1;306(11):G917-28. doi: 10.1152/ajpgi.00422.2013. Epub 2014 Apr 24.
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.
坏死性小肠结肠炎是早产儿胃肠道疾病发病率和死亡率的主要原因,其特征是最初出现喂养不耐受和腹胀,随后迅速发展为肠凝固性坏死,许多情况下导致死亡。尽管 NEC 发展的风险因素仍然被广泛接受,即早产和配方奶喂养,但潜在机制仍不完全清楚。目前的观点表明,NEC 是由于早产儿宿主的黏膜免疫系统与异常的本土微生物群之间的异常相互作用而发展起来的,导致黏膜炎症反应过度和肠系膜灌注受损。为了了解导致 NEC 的分子和细胞事件,已经开发了各种动物模型。然而,可用动物模型的数量和变异性以及每种模型的独特特征,引发了关于特定模型在 NEC 研究中的有效性的重要问题。为了试图为不断增长的 NEC 研究人员群体提供一些指导,我们现在试图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,并评估每种模型的优点、缺点、挑战和主要科学发现。提出了一种模型验证策略,对主要模型进行了比较,并探讨了 NEC 研究领域的未来方向和挑战。