Document Detail


Biochemical and morphological changes in the digestive tract of rats after prenatal and postnatal malnutrition.
MedLine Citation:
PMID:  2502904     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Six-week-old rats subjected to prenatal and postnatal dietary restriction (maternal and weanling intake = 50% that of controls) were studied. Compared with controls, malnourished rats not only had reduced body (78 +/- 12 vs 187 +/- 21 g) and organ weights (small intestine: 4.51 +/- 0.46 vs 9.89 +/- 0.61 g; colon: 0.75 +/- 0.08 vs 1.77 +/- 0.18 g; liver: 2.75 +/- 0.34 vs 9.13 +/- 1.33 g; pancreas: 0.78 +/- 0.14 vs 1.67 +/- 0.49 g) but also decreased body weight-length ratios (6.5 +/- 0.3 vs 10.8 +/- 1.4 g/cm) and serum albumin levels. The small intestinal mucosa was hypotrophic (protein-DNA ratio: 5.02 +/- 1.43 vs 8.82 +/- 0.68, malnourished vs controls, respectively) with reduced mucosal thickness, villus height, and crypt depth. Specific activities of lactase, maltase, and sucrase were diminished (53%, 66%, 54% of control values, respectively). Colonic mucosa was hypoplastic with decreased mucosal thickness and crypt depth. Liver and pancreas were both hypotrophic and hypoplastic. The findings suggest that, in contrast to colonic mucosa, pancreas, and liver, the small intestinal mucosa maintained cell number during prolonged prenatal and postnatal malnutrition.
Authors:
A Firmansyah; L Suwandito; D Penn; E Lebenthal
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, Non-P.H.S.    
Journal Detail:
Title:  The American journal of clinical nutrition     Volume:  50     ISSN:  0002-9165     ISO Abbreviation:  Am. J. Clin. Nutr.     Publication Date:  1989 Aug 
Date Detail:
Created Date:  1989-09-07     Completed Date:  1989-09-07     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0376027     Medline TA:  Am J Clin Nutr     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  261-8     Citation Subset:  AIM; IM    
Affiliation:
International Institute for Infant Nutrition and Gastrointestinal Disease, Children's Hospital of Buffalo, NY 14222.
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MeSH Terms
Descriptor/Qualifier:
Animals
Animals, Newborn / growth & development*
Colon / metabolism,  pathology
DNA / analysis
Digestive System / metabolism*,  pathology
Female
Intestinal Mucosa / enzymology
Intestine, Small / metabolism,  pathology
Liver / metabolism,  pathology
Nutrition Disorders / metabolism*,  pathology
Organ Size
Pancreas / metabolism,  pathology
Pregnancy
Prenatal Exposure Delayed Effects*
Proteins / analysis
Rats
Rats, Inbred Strains
Sucrase / metabolism
alpha-Glucosidases / metabolism
beta-Galactosidase / metabolism
Chemical
Reg. No./Substance:
0/Proteins; 9007-49-2/DNA; EC 3.2.1.20/alpha-Glucosidases; EC 3.2.1.23/beta-Galactosidase; EC 3.2.1.48/Sucrase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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