Experimentally induced gluten enteropathy and protective effect of epidermal growth factor in artificially fed neonatal rats

Journal of Pediatric Gastroenterology and Nutrition

Volumn 36, Issue 1, 2003, Pages 96-104

  Stepankova, Renata ^a   Kofroňová, Olga ^a   Tučková, Ludmila ^a   Kozáková, Hana ^a   Cebra, John J ^b   Tlaskalová Hogenová, Helena ^a  

^a INSTITUTE OF MICROBIOLOGY   (Czech Republic)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Celiac disease; Epidermal growth factor; Interferon

Indexed keywords

EPIDERMAL GROWTH FACTOR; GAMMA INTERFERON; GLIADIN; GLUTEN; RECOMBINANT EPIDERMAL GROWTH FACTOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; ATROPHY; CONTROLLED STUDY; DIET; ENTEROPATHY; EXPERIMENTATION; FEEDING BEHAVIOR; INBRED STRAIN; INFLAMMATORY CELL; INTESTINE INJURY; INTESTINE VILLUS; MILK; NONHUMAN; PRIORITY JOURNAL; RAT; T LYMPHOCYTE; ANIMAL; BODY WEIGHT; CELIAC DISEASE; CHEMICALLY INDUCED DISORDER; DISEASE MODEL; DRUG EFFECT; JEJUNUM; NEWBORN; NUTRITIONAL SUPPORT; PHYSIOLOGY; RAT STRAIN; SCANNING ELECTRON MICROSCOPY; SUCKLING; TIME; ULTRASTRUCTURE;

ANIMALIA;

ANIMALS; ANIMALS, NEWBORN; ANIMALS, SUCKLING; BODY WEIGHT; CELIAC DISEASE; DISEASE MODELS, ANIMAL; EPIDERMAL GROWTH FACTOR; GLIADIN; JEJUNUM; MICROSCOPY, ELECTRON, SCANNING; NUTRITIONAL SUPPORT; RATS; RATS, INBRED STRAINS; TIME FACTORS;

EID: 19044383571     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005176-200301000-00018     Document Type: Article

References (33)

1. Marsh MN. Gluten, major histocompatibility complex, and the small intestine: A molecular and immunobiologic approach to the spectrum of gluten sensitivity "celiac sprue." Gastroenterology 1992;102:330-54.
2. Hekkens WT. The toxicity of wheat prolamins. Ann Nestle 1993;51-8.
3. Kasarda DD. Gluten and gliadin: Precipitating factors in celiac disease. In: Mäki M, Collin P, Visakorpi JK, eds. Celiac disease. Celiac Disease Study Group, Tampere, Finland; 1997:95-212.
4. Štěpánková R, Tlaskalová H, Sinkora J, Jodl J, Frič P. Changes in jejunal mucosa after long-term feeding of germfree rats with gluten. Scand J Gastroenterol 1996;31:551-7.
5. Troncone R, Ferguson A. Animal model of gluten induced enteropathy in mice. Gut 1991;32:871-5.
6. Marsh MN, Morgan S, Moriarty KJ, Ensari A. Intestinal lymphocyte responses to in vivo gluten challenge. In: Mäki MP, Collin P, Visakorpi JK, eds. Celiac disease. Celiac Disease Study Group, Tampere, Finland; 1997:125-37.
7. Auricchio S, Follo D, De Ritis G, et al. Does breast feeding protect against the development of clinical symptoms of caliac disease in children? J Pediatr Gastroenterol Nutr 1983;2:428-33.
8. Greco L, Mayer M, Grimaldi M, Follo D, De Ritis G, Auricchio S. The effect of early feeding on the onset of symptoms in celiac disease. J Pediatr Gastroenterol Nutr 1985;4:52-5
9. Mäki M, Holm K. Incidence and prevalence of celiac disease in Tampere: Celiac disease is not disappearing. Acta Paediatr Scand 1990;79:980-2.
10. Dvořák B, Koldovský O. Concerning the physiological role of milk-born transforming growth factor-α for the neonate. Endocr Regul 1993;27:145-7.
11. Štěpánková R, Šterzl J, Trebichavský I. Long-term effect on the immune status of defined diets during the early postnatal period in rat. Physiol Bohemoslov 1985;34:49-61.
12. Štěpánková R, Dvořák B, Šterzl J, Trebichavský I. Effects of essential fatty acid deficiency in milk diets on the development of germfree and conventional rats. Physiol Bohemoslov 1990;39: 135-46.
13. Dvořák B, Štěpánková R. Effects of dietary essential fatty acid deficiency on the development of rat thymus and immune system. Prostaglandins Leucotrienes Essential Fatty Acids 1992;46:183-9.
14. Štěpánková R. Weaning of hand-fed GF animals. In: Lefkovits I, Tlaskalová H, Sterzl J, eds. Immunology Methods Manual. Gnotobiologic Models. New York: Academy Press, 1997:1541.
15. Mölberg O, Kett K, Scott H, Thorsby E, Sollid LM, Lundin KEA. Gliadin specific, HLA-DQ2-restricted T cells are commonly found in small intestine biopsies from celiac disease patients, but not from controls. Scand J Immunol 1997;46:103-9.
16. Sollid LM, Lundin KEA, Sjöström H, Mölberg O, Thorsby E. HLA-DQ molecules, peptides and T cells in celiac disease. In: Mäki M, Collin P, Visakorpi JK, eds. Celiac Disease. Celiac Disease Study Group, Tampere, Finland; 1997:265-74.
17. Hall EJ, Batt RM. Dietary modulation of gluten sensitivity in a naturally occurring enteropathy of Irish setter dogs. Gut 1992;33: 198-205.
18. Troncone R, Caputo N, Zibella A, Molitierno G, Maiuri L, Auricchio S. Effects of gluten enriched diet on the small intestinal mucosa of normal mice and mice with graft versus host reaction. Gut 1994;35:779-89.
19. Simonski K, Gonnella P, Bernanke J, Owen L, Neutra M, Murphy RA. Uptake and transepithelial transport of nerve growth factor in suckling rat ileum. J Cell Biol 1986;103:1976-90.
20. Moxey PC, Trier JS. Development of villus absorptive cells in the human fetal small intestine: A morphologic and morphometric study. Anat Rec 1979;195:463-82.
21. Van Elburg RM, Uil JJ, De Monchy GR, Heymans HSA. Intestinal permeability in pediatric gastroenterology. Scand J Gastroenterol 1992;27(suppl 194):19-24.
22. Sütas Y, Aution S, Rantala I, Isolauri E. IFN-gamma enhances macromolecular transport across Peyer's patches in suckling rats: Implications for natural immune responses to dietary antigens early in life. J Pediatr Gastroenterol Nutr 1997;24:162-9.
23. Schaudies RP, Grimes J, Wray HL, Koldovský O. Gastrointestinal absorption of epidermal growth factor in suckling rats. Am J Physiol 1990;259:G1056-61.
24. Dvořák B, Holubec H, LeBouton AV, Wilson JM, Koldovský O. Epidermal growth factor and transforming growth factor-α m RNA in rat small intestine: In situ hybridization study. FEBS Lett 1994; 352:291-5.
25. Hormi K, Lehy T. Transforming growth factor-α in vivo stimulates epithelial cell proliferation in digestive tissues of suckling rats. Gut 1996;39:532-8.
26. Playford RJ, Hanby AM, Geschmeissner S, Peiffer LP, Wright NA, McGarrity T. The epidermal growth factor receptor (EGF-R) is present on the basolateral, but not the apical, surface of enterocytes in the human gastrointestinal tract. Gut 1996;39:262-6.
27. Montaner B, Perez-Tomas R. Epidermal growth factor receptor (EGF-R) localization in the apical membrane of the enterocytes of rat duodenum. Cell Biol Int 1999;23:475-9.
28. Playford RJ, Wright NA. Why is epidermal growth factor present in the gut lumen? Gut 1996;38:303-5.
29. Playford RJ, Macdonald CE, Johonson WS. Colostrum and milk-derived peptide growth factors for the treatment of gastrointestinal disorders. Am J Clin Nutr 2000;72:5-14.
30. Dvorak B, Halpern MD, Holubec H, et al. Epidermal growth factor reduces the development of necrotizing enterocolitis in a neonatal rat model. Am J Physiol Gastrointest Liver Physiol 2002;282: G156-64.
31. Dignass AU, Sturm A. Peptide growth factors in the intestine. Eur J Gastroenterol Hepatol 2001;13:763-70.
32. Familari M, Cook GA, Taupin DR, Marryatt G, Yeomans ND, Giraud AS. Trefoil peptides are early markers of gastrointestinal maturation in the rat. Int J Dev Biol 1998;42:783-9.
33. Tran CP, Cook GA, Yeomans ND, Thim L, Giraud AS. Trefoil peptide TFF2 (spasmolytic polypeptide) potently accelerates healing and reduces inflammation in a rat model of colitis. Gut 1999; 44:636.