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1
Early weaning stress induces chronic functional diarrhea, intestinal barrier defects, and increased mast cell activity in a porcine model of early life adversity.早期断奶应激在仔猪生命早期逆境模型中诱导慢性功能性腹泻、肠道屏障缺陷和肥大细胞活性增加。
Neurogastroenterol Motil. 2017 Nov;29(11). doi: 10.1111/nmo.13118. Epub 2017 Jun 1.
2
Large Animal Models: The Key to Translational Discovery in Digestive Disease Research.大型动物模型:消化系统疾病研究中转化性发现的关键
Cell Mol Gastroenterol Hepatol. 2016 Nov;2(6):716-724. doi: 10.1016/j.jcmgh.2016.09.003.
3
The arachidonic acid metabolite 11β-ProstaglandinF2α controls intestinal epithelial healing: deficiency in patients with Crohn's disease.花生四烯酸代谢产物11β-前列腺素F2α调控肠道上皮愈合:克罗恩病患者存在该物质缺乏
Sci Rep. 2016 May 3;6:25203. doi: 10.1038/srep25203.
4
Postnatal development of the myenteric glial network and its modulation by butyrate.肠肌间神经胶质网络的产后发育及其受丁酸盐的调节。
Am J Physiol Gastrointest Liver Physiol. 2016 Jun 1;310(11):G941-51. doi: 10.1152/ajpgi.00232.2015. Epub 2016 Apr 7.
5
Early-life stress origins of gastrointestinal disease: animal models, intestinal pathophysiology, and translational implications.胃肠道疾病的早期生活应激源:动物模型、肠道病理生理学及转化意义
Am J Physiol Gastrointest Liver Physiol. 2015 Dec 15;309(12):G927-41. doi: 10.1152/ajpgi.00206.2015. Epub 2015 Oct 8.
6
Emerging roles of gut microbiota and the immune system in the development of the enteric nervous system.肠道微生物群和免疫系统在肠神经系统发育中的新作用。
J Clin Invest. 2015 Mar 2;125(3):956-64. doi: 10.1172/JCI76308.
7
Porcine models of digestive disease: the future of large animal translational research.猪消化系统疾病模型:大型动物转化研究的未来。
Transl Res. 2015 Jul;166(1):12-27. doi: 10.1016/j.trsl.2015.01.004. Epub 2015 Jan 13.
8
Microbiota controls the homeostasis of glial cells in the gut lamina propria.微生物群控制肠道固有层神经胶质细胞的动态平衡。
Neuron. 2015 Jan 21;85(2):289-95. doi: 10.1016/j.neuron.2014.12.037. Epub 2015 Jan 8.
9
The enteric nervous system and gastrointestinal innervation: integrated local and central control.肠神经系统和胃肠道神经支配:局部和中枢的综合控制。
Adv Exp Med Biol. 2014;817:39-71. doi: 10.1007/978-1-4939-0897-4_3.
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Small intestinal permeability is increased in diarrhoea predominant IBS, while alterations in gastroduodenal permeability in all IBS subtypes are largely attributable to confounders.在腹泻型肠易激综合征中,小肠通透性增加,而所有肠易激综合征亚型的胃十二指肠通透性改变在很大程度上归因于混杂因素。
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肠道屏障功能障碍与复发性消化道疾病:来自早期生活应激猪模型的启示。

Impaired intestinal barrier function and relapsing digestive disease: Lessons from a porcine model of early life stress.

机构信息

Department of Clinical Sciences, Center for Gastrointestinal Biology and Disease, College of Veterinary Medicine, NC State University, Raleigh, NC, USA.

出版信息

Neurogastroenterol Motil. 2017 Nov;29(11):1-4. doi: 10.1111/nmo.13216.

DOI:10.1111/nmo.13216
PMID:29052972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5940449/
Abstract

Within this issue of Neurogastroenterology and Motility, an article by Pohl et al highlights new insights from a powerful porcine model of the link between early life adversity and relapsing functional gastrointestinal disorders. Early weaning stress closely mimics the early life psychosocial stressors that have been linked to adult onset gastrointestinal dysfunction. This early weaning model provides reproducible and highly translatable outcomes in young stress-challenged pigs. Due to the convincingly comparable neurological and gastroenterological anatomy and physiology between pigs and human beings, gastrointestinal stress and injury studies utilizing swine models will provide invaluable insights to improve our understanding and treatment of gastrointestinal disease in human beings. Future studies to examine mechanisms underlying this link between early life adversity and functional gastrointestinal disorders will explore the roles of gender and hypomaturity in gastrointestinal responses to stress.

摘要

本期《神经胃肠病学与动力学期刊》中,Pohl 等人的一篇文章强调了一种强大的猪模型在早期生活逆境与复发性功能性胃肠疾病之间关联的新见解。早期断奶应激非常类似于与成年期胃肠道功能障碍相关的早期生活心理社会应激源。这种早期断奶模型为处于应激挑战中的年轻猪提供了可重现且高度可转化的结果。由于猪和人类在神经和胃肠解剖学和生理学上具有令人信服的可比性,利用猪模型进行胃肠道应激和损伤研究将为我们深入理解和治疗人类胃肠道疾病提供宝贵的见解。未来研究将探索早期生活逆境与功能性胃肠疾病之间这种关联的机制,探索性别和不成熟在胃肠道对压力反应中的作用。