Document Detail


Colon luminal content and epithelial cell morphology are markedly modified in rats fed with a high-protein diet.
MedLine Citation:
PMID:  20689060     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Hyperproteic diets are used in human nutrition to obtain body weight reduction. Although increased protein ingestion results in an increased transfer of proteins from the small to the large intestine, there is little information on the consequences of the use of such diets on the composition of large intestine content and on epithelial cell morphology and metabolism. Rats were fed for 15 days with either a normoproteic (NP, 14% protein) or a hyperproteic isocaloric diet (HP, 53% protein), and absorptive colonocytes were observed by electron microscopy or isolated for enzyme activity studies. The colonic luminal content was recovered for biochemical analysis. Absorbing colonocytes were characterized by a 1.7-fold reduction in the height of the brush-border membranes (P = 0.0001) after HP diet consumption when compared with NP. This coincided in the whole colon content of HP animals with a 1.8-fold higher mass content (P = 0.0020), a 2.2-fold higher water content (P = 0.0240), a 5.2-fold higher protease activity (P = 0.0104), a 5.5-fold higher ammonia content (P = 0.0008), and a more than twofold higher propionate, valerate, isobutyrate, and isovalerate content (P < 0.05). The basal oxygen consumption of colonocytes was similar in the NP and HP groups, but ammonia was found to provoke a dose-dependent decrease of oxygen consumption in the isolated absorbing colonocytes. The activity of glutamine synthetase (which condenses ammonia and glutamate) was found to be much higher in colonocytes than in small intestine enterocytes and was 1.6-fold higher (P = 0.0304) in colonocytes isolated from HP animals than NP. Glutaminase activity remained unchanged. Thus hyperproteic diet ingestion causes marked changes both in the luminal environment of colonocytes and in the characteristics of these cells, demonstrating that hyperproteic diet interferes with colonocyte metabolism and morphology. Possible causal relationships between energy metabolism, reduced height of colonocyte brush-border membranes, and reduced water absorption are discussed.
Authors:
Mireille Andriamihaja; Anne-Marie Davila; Mamy Eklou-Lawson; Nathalie Petit; Serge Delpal; Fadhila Allek; Anne Blais; Corine Delteil; Daniel Tomé; François Blachier
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-08-05
Journal Detail:
Title:  American journal of physiology. Gastrointestinal and liver physiology     Volume:  299     ISSN:  1522-1547     ISO Abbreviation:  Am. J. Physiol. Gastrointest. Liver Physiol.     Publication Date:  2010 Nov 
Date Detail:
Created Date:  2010-10-29     Completed Date:  2010-11-12     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100901227     Medline TA:  Am J Physiol Gastrointest Liver Physiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  G1030-7     Citation Subset:  IM    
Affiliation:
Institut National de Recherche Agronomique, AgroParisTech, Centre de Recherche en Nutrition Humaine-Ile de France, UMR 914 Physiologie de Nutrition et du Comportement Alimentaire, Paris, France.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Ammonia / analysis,  pharmacology
Animals
Body Water
Cell Shape / drug effects*
Colon / drug effects*,  metabolism
Dietary Proteins / administration & dosage,  metabolism*
Epithelial Cells / drug effects*,  physiology
Gastrointestinal Contents / chemistry,  drug effects*
Glutamate-Ammonia Ligase / metabolism
Male
Oxygen Consumption / drug effects
Rats
Rats, Wistar
Chemical
Reg. No./Substance:
0/Dietary Proteins; 7664-41-7/Ammonia; EC 6.3.1.2/Glutamate-Ammonia Ligase

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


Previous Document:  HIF-1 mediates pathogenic inflammatory responses to intestinal ischemia-reperfusion injury.
Next Document:  Roles of lysosomal proteolytic systems in AQP5 degradation in the submandibular gland of rats follow...