Document Detail


Isolated canine and murine intestinal cells exhibit a different pattern of fuel utilization for oxidative metabolism.
MedLine Citation:
PMID:  12019609     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The amount and type of dietary fiber influences the end-products of fermentation and thus fuel availability to intestinal tissue. Metabolic fuel usage was studied in intestinal cells isolated from dogs consuming a commercial diet or from rats consuming either a commercial rat diet or dog diet to examine preferential fuel usage, the effect of diet, and species differences. Production of 14CO2 was measured by incubating cells in media containing either D-[U-14C]glucose, [1-14C]n-butyrate, L-[U-14C]glutamine, or [1-14C]propionate with or without competing substrates. The presence of a mixture of 5 mM each of glucose, butyrate, propionate, and acetate and 1 mM glutamine in the media decreased CO2 production from glucose, glutamine, and propionate by canine enterocytes (P < 0.05) and from glutamine and propionate by canine colonocytes (P < 0.05). The presence of glutamine in the media decreased glucose oxidation by murine enterocytes, regardless of the diet. Similarly, glutamine decreased glucose oxidation by murine colonocytes (P < 0.05), but only when the rats had consumed the rat diet. Regardless of diet, murine colonocytes oxidized more butyrate (P < 0.01) than did enterocytes, and murine enterocytes tended (P < 0.07) to oxidize more glucose than did colonocytes. The proportion of propionate in colonic contents was higher in dogs than in rats (P < 0.02), and the proportion of butyrate tended to be higher in contents from rats than in those from dogs (P < 0.08). Colonic and cecal wet weights were decreased (P < 0.05) when rats were fed the commercial dog diet. Preferred utilization of substrates by isolated canine enterocytes and colonocytes differed from that of murine intestinal cells. These differences were only partially overcome by feeding the same diet to each species.
Authors:
A D Beaulieu; J K Drackley; T R Overton; L S Emmert
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Journal of animal science     Volume:  80     ISSN:  0021-8812     ISO Abbreviation:  J. Anim. Sci.     Publication Date:  2002 May 
Date Detail:
Created Date:  2002-05-21     Completed Date:  2002-10-02     Revised Date:  2003-11-14    
Medline Journal Info:
Nlm Unique ID:  8003002     Medline TA:  J Anim Sci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1223-32     Citation Subset:  IM    
Affiliation:
Department of Animal Sciences, University of Illinois, Urbana 61801, USA.
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MeSH Terms
Descriptor/Qualifier:
Acetates / metabolism
Animals
Butyric Acids / metabolism
Carbon Dioxide / metabolism
Carbon Isotopes
Cells, Cultured
Colon / cytology*,  metabolism*
Diet / veterinary*
Dietary Fiber / metabolism
Dogs
Enterocytes / metabolism
Fermentation
Glucose / metabolism
Glutamine / metabolism
Intestine, Small / cytology*,  metabolism*
Male
Models, Animal
Oxidation-Reduction
Oxygen Consumption*
Propionates / metabolism
Rats
Rats, Sprague-Dawley
Species Specificity
Chemical
Reg. No./Substance:
0/Acetates; 0/Butyric Acids; 0/Carbon Isotopes; 0/Propionates; 124-38-9/Carbon Dioxide; 50-99-7/Glucose; 56-85-9/Glutamine

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


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