Nutritional programming of gastrointestinal tract development. Is the pig a good model for man?

被引:250
作者
Guilloteau, Paul [1 ]
Zabielski, Romuald [2 ]
Hammon, Harald M. [3 ]
Metges, Cornelia C. [3 ]
机构
[1] INRA, U1079, UMR SENAH, F-35590 Domaine De La Prise, Saint Gilles, France
[2] Warsaw Univ Life Sci, Fac Vet Med, Dept Physiol Sci, Warsaw, Poland
[3] Leibniz Inst Farm Anim Biol FBN, Res Unit Nutr Physiol, D-18196 Dummerstorf, Germany
关键词
Intra-uterine growth retardation; Animal models; Swine; Human nutrition; INTRAUTERINE GROWTH-RETARDATION; ADIPOSE-TISSUE DEVELOPMENT; MATERNO-FETAL EXCHANGES; LONG-TERM CONSEQUENCES; LOW-PROTEIN-DIET; ANIMAL-MODELS; BIRTH-WEIGHT; GESTATIONAL-AGE; ENZYME-ACTIVITIES; EARLY-LIFE;
D O I
10.1017/S0954422410000077
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The consequences of early-life nutritional programming in man and other mammalian species have been studied chiefly at the metabolic level. Very few studies, if any, have been performed in the gastrointestinal tract (GIT) as the target organ, but extensive GIT studies are needed since the GIT plays a key role in nutrient supply and has an impact on functions of the entire organism. The possible deleterious effects of nutritional programming at the metabolic level were discovered following epidemiological studies in human subjects, and confirmed in animal models. Investigating the impact of programming on GIT structure and function would need appropriate animal models due to ethical restrictions in the use of human subjects. The aim of the present review is to discuss the use of pigs as an animal model as a compromise between ethically acceptable animal studies and the requirement of data which can be interpolated to the human situation. In nutritional programming studies, rodents are the most frequently used model for man, but GIT development and digestive function in rodents are considerably different from those in man. In that aspect, the pig GIT is much closer to the human than that of rodents. The swine species is closely comparable with man in many nutritional and digestive aspects, and thus provides ample opportunity to be used in investigations on the consequences of nutritional programming for the GIT. In particular. the 'sow-piglets' dyad could be a useful tool to simulate the 'human mother-infant' dyad in studies which examine short-, middle- and long-term effects and is suggested as the reference model.
引用
收藏
页码:4 / 22
页数:19
相关论文
共 231 条
[1]   Morphological changes and increased sucrase and isomaltase activity in small intestines of insulin-deficient and type 2 diabetic rats [J].
Adachi, T ;
Mori, C ;
Sakurai, K ;
Shihara, N ;
Tsuda, K ;
Yasuda, K .
ENDOCRINE JOURNAL, 2003, 50 (03) :271-279
[2]   Size at birth and growth trajectories to young adulthood [J].
Adair, Linda S. .
AMERICAN JOURNAL OF HUMAN BIOLOGY, 2007, 19 (03) :327-337
[3]   Enteral feeding and gut atrophy [J].
Alpers, DH .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2002, 5 (06) :679-683
[4]  
ALUMETS J, 1983, GASTROENTEROLOGY, V85, P1359
[5]  
[Anonymous], 1975, FAMINE HUM DEV DUTCH
[6]  
[Anonymous], 2005, DIETARY REFERENCE IN, DOI DOI 10.17226/10490
[7]   Experimental models of developmental programming: consequences of exposure to an energy rich diet during development [J].
Armitage, JA ;
Taylor, PD ;
Poston, L .
JOURNAL OF PHYSIOLOGY-LONDON, 2005, 565 (01) :3-8
[8]   Developmental programming of the metabolic syndrome by maternal nutritional imbalance: how strong is the evidence from experimental models in mammals? [J].
Armitage, JA ;
Khan, IY ;
Taylor, PD ;
Nathanielsz, PW ;
Poston, L .
JOURNAL OF PHYSIOLOGY-LONDON, 2004, 561 (02) :355-377
[9]  
Armitage JA, 2004, J SOC GYNECOL INVEST, V11, p183A
[10]   Presence of obestatin in breast milk: Relationship among obestatin, ghrelin, and leptin in lactating women [J].
Aydin, Suleyman ;
Ozkan, Yusuf ;
Erman, Fazilet ;
Gurates, Bilgin ;
Kilic, Nermin ;
Colak, Ramis ;
Gundogan, Tugba ;
Catak, Zekiye ;
Bozkurt, Mahmut ;
Akin, Okhan ;
Sen, Yasar ;
Sahn, Ibrahim .
NUTRITION, 2008, 24 (7-8) :689-693