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Am J Physiol ; 273(4): G913-9, 1997 10.
Article in English | MEDLINE | ID: mdl-9357835

ABSTRACT

In a rabbit model of chronic ileal inflammation, we previously demonstrated that coupled NaCl absorption was reduced because of an inhibition of Cl-/HCO3- but not Na+/H+ exchange on the brush-border membrane (BBM) of villus cells. In this study we determined the alterations in Na+-stimulated glucose [Na+-O-methyl-D-glucose (Na+-OMG)] absorption during chronic ileitis. Na+-OMG uptake was reduced in villus cells from the chronically inflamed ileum. Na+-K+-adenosinetriphosphatase (ATPase), which provides the favorable Na+ gradient for this cotransporter in intact cells, was found to be reduced also. However, in villus cell BBM vesicles from the inflamed ileum Na+-OMG uptake was reduced as well, suggesting an effect at the level of the cotransporter itself. Kinetic studies demonstrated that Na+-OMG uptake in the inflamed ileum was inhibited by a decrease in the maximal rate of uptake for OMG without a change in the affinity. Analysis of steady-state mRNA and immunoreactive protein levels of this cotransporter demonstrates reduced expression. Thus Na+-glucose cotransport was inhibited in the chronically inflamed ileum, and the inhibition was secondary to a decrease in the number of cotransporters and not solely secondary to an inhibition of Na+-K--ATPase or altered affinity for glucose.


Subject(s)
Coccidiosis/physiopathology , Ileitis/physiopathology , Intestinal Mucosa/metabolism , Membrane Glycoproteins/biosynthesis , Monosaccharide Transport Proteins/biosynthesis , Monosaccharide Transport Proteins/metabolism , Sodium/metabolism , Animals , Coccidiosis/pathology , Eimeria , Ileitis/parasitology , Ileum , Inflammation , Intestinal Absorption , Intestinal Mucosa/pathology , Kinetics , Methylglucosides/metabolism , Microvilli/metabolism , Monosaccharide Transport Proteins/antagonists & inhibitors , RNA, Messenger/biosynthesis , Rabbits , Sodium-Glucose Transporter 1 , Sodium-Potassium-Exchanging ATPase/metabolism , Transcription, Genetic
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