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Am J Physiol Gastrointest Liver Physiol 288: G431-G438, 2005. First published September 23, 2004; doi:10.1152/ajpgi.00242.2004
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HORMONES AND SIGNALING

Nutrient-stimulated GLP-2 release and crypt cell proliferation in experimental short bowel syndrome

G. R. Martin,1 L. E. Wallace,1 B. Hartmann,2 J. J. Holst,2 L. Demchyshyn,3 K. Toney,3 and D. L. Sigalet1

1University of Calgary, Gastrointestinal Research Group, Calgary, Alberta, Canada; 2Department of Medical Physiology, The Panum Institute, University of Copenhagen, Copenhagen, Denmark; and 3NPS Pharmaceuticals, Mississauga, Ontario, Canada

Submitted 1 June 2004 ; accepted in final form 16 September 2004

Glucagon-like peptide-2 (GLP-2) is an enteroendocrine peptide that is released in response to luminal nutrients and has unique trophic actions in the gastrointestinal tract. These features suggest GLP-2 may be important in controlling intestinal adaptation. We examined the relationship over time of GLP-2 production and adaptation to intestinal resection, the effects of resection-induced malabsorption on GLP-2 production, and the correlation of endogenous serum GLP-2 levels with adaptation as measured by crypt-cell proliferation (CCP). We initially examined the effect of nutrient malabsorption, induced by a 90% resection of the proximal intestine studied on day 4, on the time course and levels of GLP-2 release. Secondly, the degree of malabsorption was varied by performing intestinal transection or 50, 75, or 90% resection of proximal small intestine. Finally, the relationship of GLP-2 levels over time with adaptation to a 90% resection was examined by determining GLP-2 levels on days 7, 14, and 28, and correlating this with intestinal adaptation, as assessed by morphology and CCP rate. A 90% resection significantly increased basal and postprandial GLP-2 levels, with a net increase in nutrient-stimulated exposure over 90 min; GLP-2 exposure (integrated levels vs. time) increased 12.7-fold in resected animals (P < 0.001). Basal and postprandial GLP-2 levels significantly correlated with the magnitude of intestinal resection (r2 = 0.71; P < 0.001), CCP (r2 = 0.48; P < 0.005), and nutrient malabsorption (protein, P < 0.001; fat, P < 0.005). The increase in CCP was maintained to 28 days after small bowel resection and was associated with an ongoing elevation in GLP-2 release. These findings suggest that GLP-2 is important in initiating and maintaining the small intestinal adaptive response to resection.

nutrient malabsorption; intestinal adaptation; intestinal resection; intestinal morphology; nutrition



Address for reprint requests and other correspondence: G. R. Martin, Health Sciences Bldg, Rm. 1746, 3330 Hospital Dr. NW, Calgary, AB, Canada T2N 4N1 (E-mail: marting{at}ucalgary.ca)




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