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本文引用的文献

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Gut microbiomes of Malawian twin pairs discordant for kwashiorkor.马拉维双胞胎中库普弗细胞营养不良症的肠道微生物组。
Science. 2013 Feb 1;339(6119):548-54. doi: 10.1126/science.1229000. Epub 2013 Jan 30.
2
Liver protein expression in dairy cows with high liver triglycerides in early lactation.泌乳早期高甘油三酯奶牛肝脏蛋白质表达。
J Dairy Sci. 2012 May;95(5):2409-21. doi: 10.3168/jds.2011-4604.
3
Effects on Rats of Prolonged Staple African Diet.长期食用非洲主食对大鼠的影响。
Br Med J. 1944 Jan 29;1(4334):149-50. doi: 10.1136/bmj.1.4334.149-a.
4
The gut takes nearly all: threonine kinetics in infants.肠道几乎摄取了全部:婴儿体内苏氨酸的动力学
Am J Clin Nutr. 2007 Oct;86(4):1132-8. doi: 10.1093/ajcn/86.4.1132.
5
Antimicrobial treatment reduces intestinal microflora and improves protein digestive capacity without changes in villous structure in weanling pigs.抗菌治疗可减少断奶仔猪的肠道微生物群,并提高蛋白质消化能力,而不改变绒毛结构。
Br J Nutr. 2007 Jun;97(6):1128-37. doi: 10.1017/S0007114507691910. Epub 2007 Mar 21.
6
Methionine transmethylation and transsulfuration in the piglet gastrointestinal tract.仔猪胃肠道中的蛋氨酸转甲基作用和转硫作用。
Proc Natl Acad Sci U S A. 2007 Feb 27;104(9):3408-13. doi: 10.1073/pnas.0607965104. Epub 2007 Feb 21.
7
Lipid metabolism and liver inflammation. II. Fatty liver disease and fatty acid oxidation.脂质代谢与肝脏炎症。二、脂肪肝疾病与脂肪酸氧化。
Am J Physiol Gastrointest Liver Physiol. 2006 May;290(5):G852-8. doi: 10.1152/ajpgi.00521.2005.
8
Measuring splanchnic amino acid metabolism in vivo using stable isotopic tracers.使用稳定同位素示踪剂在体内测量内脏氨基酸代谢。
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9
THE ANAEMIA OF KWASHIORKOR IN UGANDA.乌干达夸休可尔症贫血症
Trans R Soc Trop Med Hyg. 1965 May;59:326-41. doi: 10.1016/0035-9203(65)90015-5.
10
EFFECT OF DIETARY ENERGY INTAKE ON PROTEIN DEFICIENCY SYMPTOMS AND BODY COMPOSITION OF BABY PIGS FED EQUALIZED BUT SUBOPTIMAL AMOUNTS OF PROTEIN.日粮能量摄入量对摄入等量但低于最佳水平蛋白质的仔猪蛋白质缺乏症状及身体组成的影响。
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营养不良可导致肠道萎缩和肝脂肪浸润增加:在儿童营养不良猪模型中的研究。

Malnutrition induces gut atrophy and increases hepatic fat infiltration: studies in a pig model of childhood malnutrition.

机构信息

Department of Nutrition, Exercise and Sports, University of Copenhagen 30 Rolighedsvej, DK-1958 Frederiksberg C, Denmark.

出版信息

Am J Transl Res. 2013 Aug 15;5(5):543-54. eCollection 2013.

PMID:23977413
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3745441/
Abstract

Childhood malnutrition is a problem in developing countries, and pathological changes in digestive organs such as the intestine and liver are poorly understood. An animal model to study the progression of severe acute malnutrition could elucidate pathological changes in the intestine and liver. We sought to characterize growth and clinical changes during malnutrition related to structural and functional indices in the intestine and liver. Newly weaned piglets were given ad libitum access to a maize flour diet (MAIZE, n=9) or a nutritionally optimized reference diet (REFERENCE, n=12) for 7 weeks. Growth, hematology and clinical biochemistry where recorded weekly. After 7 weeks, the MAIZE pigs had lower body weights than the REF pigs (8.3 kg vs. 32.4 kg, P < 0.001), indicating severe stunting and moderate to severe wasting. This was paralleled by lower values for hematocrit, hemoglobin and mean cell volume in MAIZE vs. REFERENCE (P < 0.01), indicating anemia. Although the observed temporal changes in MAIZE were associated with atrophy of the small intestinal mucosa (P < 0.001), digestive enzyme activity was only marginally reduced. Serum alanine aminotransferase, bilirubin and albumin were increased in the MAIZE pigs (P < 0.001), and the liver had a vacuolated appearance and tendency toward increased triglyceride content (P=0.054). We conclude that liver and intestinal indices are compromised during malnutrition and are associated with temporal changes in growth and hematological and biochemical endpoints. The pig model is relevant for malnourished infants and can act as a valuable tool for understanding the pathophysiology of malnutrition.

摘要

儿童营养不良是发展中国家的一个问题,人们对肠道和肝脏等消化器官的病变知之甚少。建立一种研究严重急性营养不良进展的动物模型,可以阐明肠道和肝脏的病变。我们试图描述与肠道和肝脏结构和功能指标相关的营养不良相关的生长和临床变化。我们让新生仔猪自由选择玉米粉饮食(MAIZE,n=9)或营养优化参考饮食(REFERENCE,n=12),喂养 7 周。每周记录生长、血液学和临床生化指标。7 周后,MAIZE 组仔猪的体重低于 REF 组(8.3kg 比 32.4kg,P<0.001),表明严重发育迟缓且存在中度至重度消瘦。这与 MAIZE 组的红细胞压积、血红蛋白和平均细胞体积值低于 REF 组(P<0.01)相对应,表明贫血。尽管 MAIZE 中观察到的时间变化与小肠黏膜萎缩有关(P<0.001),但消化酶活性仅略有降低。MAIZE 组血清丙氨酸氨基转移酶、胆红素和白蛋白升高(P<0.001),肝脏呈空泡状且有增加的甘油三酯含量趋势(P=0.054)。我们得出结论,在营养不良期间,肝脏和肠道指数受损,并与生长和血液学及生化终点的时间变化相关。猪模型与营养不良的婴儿相关,可作为了解营养不良病理生理学的有价值工具。