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Am J Physiol Gastrointest Liver Physiol 282: G241-G248, 2002; doi:10.1152/ajpgi.00310.2001
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Vol. 282, Issue 2, G241-G248, February 2002

Expression of monosaccharide transporters in intestine of diabetic humans

J. Dyer1, I. S. Wood1, A. Palejwala2, A. Ellis2, and S. P. Shirazi-Beechey1

1 Department of Veterinary Preclinical Sciences, The University of Liverpool, Liverpool L69 7ZJ; and 2 Department of Medicine, Royal Liverpool University Hospital, Liverpool L7 8XP, United Kingdom

Noninsulin-dependent diabetes mellitus (NIDDM) is an increasingly common disease, which brings a number of life-threatening complications. In rats with experimentally induced diabetes, there is an increase in the capacity of the intestine to absorb monosaccharides. We have examined the activity and the expression of monosaccharide transporters in the intestine of patients suffering from NIDDM. Na+-dependent D-glucose transport was 3.3-fold higher in brush-border membrane (BBM) vesicles isolated from duodenal biopsies of NIDDM patients compared with healthy controls. Western analysis indicated that SGLT1 and GLUT5 protein levels were also 4.3- and 4.1-fold higher in diabetic patients. This was associated with threefold increases in SGLT1 and GLUT5 mRNA measured by Northern blotting. GLUT2 mRNA levels were also increased threefold in the intestine of diabetic patients. Analysis of other BBM proteins indicated that the activity and abundance of sucrase and lactase were increased by 1.5- to 2-fold and the level of the structural proteins villin and beta -actin was enhanced 2-fold in diabetic patients compared with controls. The increase in the capacity of the intestine to absorb monosaccharides in human NIDDM is due to a combination of intestinal structural change with a specific increase in the expression of the monosaccharide transporters SGLT1, GLUT5, and GLUT2.

noninsulin-dependent diabetes mellitus; SGLT1; GLUT5; GLUT2; human intestine


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