Glucagon-like peptide-2 induces rapid digestive adaptation following intestinal resection in preterm neonates.

Short bowel syndrome (SBS) is a frequent complication after intestinal resection in infants suffering from intestinal disease. We tested whether treatment with the intestinotrophic hormone glucagon-like peptide-2 (GLP-2) increases intestinal volume and function in the period immediately following intestinal resection in preterm pigs. Preterm pigs were fed enterally for 48 h before undergoing resection of 50% of the small intestine and establishment of a jejunostomy. Following resection, pigs were maintained on total parenteral nutrition (TPN) without (SBS, n = 8) or with GLP-2 treatment (3.5 μg/kg body wt per h, SBS+GLP-2, n = 7) and compared with a group of unresected preterm pigs (control, n = 5). After 5 days of TPN, all piglets were fed enterally for 24 h, and a nutrient balance study was performed. Intestinal resection was associated with markedly reduced endogenous GLP-2 levels. GLP-2 increased the relative absorption of wet weight (46 vs. 22%), energy (79 vs. 64%), and all macronutrients (all parameters P < 0.05). These findings were supported by a 200% increase in sucrase and maltase activities, a 50% increase in small intestinal epithelial volume (P < 0.05), as well as increased DNA and protein contents and increased total protein synthesis rate in SBS+GLP-2 vs. SBS pigs (+100%, P < 0.05). Following intestinal resection in preterm pigs, GLP-2 induced structural and functional adaptation, resulting in a higher relative absorption of fluid and macronutrients. GLP-2 treatment may be a promising therapy to enhance intestinal adaptation and improve digestive function in preterm infants with jejunostomy following intestinal resection.

[1]  A. Forbes,et al.  Teduglutide reduces need for parenteral support among patients with short bowel syndrome with intestinal failure. , 2012, Gastroenterology.

[2]  P. Brubaker,et al.  The "cryptic" mechanism of action of glucagon-like peptide-2. , 2011, American journal of physiology. Gastrointestinal and liver physiology.

[3]  R. Gilroy,et al.  Randomised placebo-controlled trial of teduglutide in reducing parenteral nutrition and/or intravenous fluid requirements in patients with short bowel syndrome , 2011, Gut.

[4]  C. Sergi,et al.  Novel Neonatal Piglet Models of Surgical Short Bowel Syndrome With Intestinal Failure , 2011, Journal of pediatric gastroenterology and nutrition.

[5]  N. Kapel,et al.  Effect of recombinant human growth hormone on intestinal absorption and body composition in children with short bowel syndrome. , 2010, JPEN. Journal of parenteral and enteral nutrition.

[6]  P. Wales,et al.  Does the colon play a role in intestinal adaptation in infants with short bowel syndrome? A multiple variable analysis. , 2010, Journal of pediatric surgery.

[7]  B. Stoll,et al.  Carbohydrate maldigestion induces necrotizing enterocolitis in preterm pigs. , 2009, American journal of physiology. Gastrointestinal and liver physiology.

[8]  B. Yusta,et al.  ErbB signaling is required for the proliferative actions of GLP-2 in the murine gut. , 2009, Gastroenterology.

[9]  J. Holst,et al.  Colonic GLP-2 is not sufficient to promote jejunal adaptation in a PN-dependent rat model of human short bowel syndrome. , 2009, JPEN. Journal of parenteral and enteral nutrition.

[10]  M. Helmrath,et al.  Early but not late administration of glucagon-like peptide-2 following ileo-cecal resection augments putative intestinal stem cell expansion. , 2009, American journal of physiology. Gastrointestinal and liver physiology.

[11]  F. Cominelli Early and late gut immune responses in IBD. , 2008, Journal of pediatric gastroenterology and nutrition.

[12]  J. Bines,et al.  GLP-2 Administration Results in Increased Proliferation but Paradoxically an Adverse Outcome in a Juvenile Piglet Model of Short Bowel Syndrome , 2008, Journal of pediatric gastroenterology and nutrition.

[13]  J. Holst,et al.  Glucagon-like peptide 2 has limited efficacy to increase nutrient absorption in fetal and preterm pigs. , 2007, American journal of physiology. Regulatory, integrative and comparative physiology.

[14]  D. Tibboel,et al.  Dietary protein absorption of the small intestine in human neonates. , 2007, JPEN - Journal of Parenteral and Enteral Nutrition.

[15]  M. Helmrath,et al.  Expansion of intestinal stem cells associated with long-term adaptation following ileocecal resection in mice. , 2007, American journal of physiology. Gastrointestinal and liver physiology.

[16]  K. Urschel,et al.  A multitracer stable isotope quantification of the effects of arginine intake on whole body arginine metabolism in neonatal piglets. , 2007, American journal of physiology. Endocrinology and metabolism.

[17]  A. Francavilla,et al.  Total parenteral nutrition-related gastroenterological complications. , 2006, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

[18]  L. Wallace,et al.  Glucagon-like Peptide-2 Induces a Specific Pattern of Adaptation in Remnant Jejunum , 2006, Digestive Diseases and Sciences.

[19]  K. Tappenden,et al.  Glucagon-like Peptide 2 Stimulates Intestinal Nutrient Absorption in Parenterally Fed Newborn Pigs , 2006, Journal of pediatric gastroenterology and nutrition.

[20]  P. Brubaker,et al.  The essential role of insulin-like growth factor-1 in the intestinal tropic effects of glucagon-like peptide-2 in mice. , 2006, Gastroenterology.

[21]  O. Goulet,et al.  Short bowel syndrome and intestinal transplantation in children , 2006, Current opinion in clinical nutrition and metabolic care.

[22]  S. K. Jensen,et al.  Preterm birth makes the immature intestine sensitive to feeding-induced intestinal atrophy. , 2005, American journal of physiology. Regulatory, integrative and comparative physiology.

[23]  J. Holst,et al.  Teduglutide (ALX-0600), a dipeptidyl peptidase IV resistant glucagon-like peptide 2 analogue, improves intestinal function in short bowel syndrome patients , 2005, Gut.

[24]  A. Moore,et al.  Neonatal short bowel syndrome: a cohort study. , 2005, Journal of pediatric surgery.

[25]  J. Holst,et al.  Nutrient-stimulated GLP-2 release and crypt cell proliferation in experimental short bowel syndrome. , 2005, American journal of physiology. Gastrointestinal and liver physiology.

[26]  J. Holst,et al.  Supplementation of total parenteral nutrition with butyrate acutely increases structural aspects of intestinal adaptation after an 80% jejunoileal resection in neonatal piglets. , 2004, JPEN. Journal of parenteral and enteral nutrition.

[27]  L. Wallace,et al.  Glucagon-like peptide-2 induces intestinal adaptation in parenterally fed rats with short bowel syndrome. , 2004, American journal of physiology. Gastrointestinal and liver physiology.

[28]  T. To,et al.  Neonatal short bowel syndrome: population-based estimates of incidence and mortality rates. , 2004, Journal of pediatric surgery.

[29]  J. Holst,et al.  GLP-2-mediated up-regulation of intestinal blood flow and glucose uptake is nitric oxide-dependent in TPN-fed piglets 1. , 2003, Gastroenterology.

[30]  J. Holst,et al.  Introduction of enteral food increases plasma GLP-2 and decreases GLP-2 receptor mRNA abundance during pig development. , 2003, The Journal of nutrition.

[31]  P. Sangild,et al.  Glucagon-Like Peptide 2 Enhances Maltase-Glucoamylase and Sucrase-Isomaltase Gene Expression and Activity in Parenterally Fed Premature Neonatal Piglets , 2002, Pediatric Research.

[32]  D. Burrin,et al.  GLP-2 has differential effects on small intestine growth and function in fetal and neonatal pigs. , 2001, American journal of physiology. Regulatory, integrative and comparative physiology.

[33]  J. Holst,et al.  Glucagon-like peptide 2 improves nutrient absorption and nutritional status in short-bowel patients with no colon. , 2001, Gastroenterology.

[34]  J. Holst,et al.  GLP-2 stimulates intestinal growth in premature TPN-fed pigs by suppressing proteolysis and apoptosis. , 2000, American journal of physiology. Gastrointestinal and liver physiology.

[35]  J. Holst,et al.  Elevated plasma glucagon-like peptide 1 and 2 concentrations in ileum resected short bowel patients with a preserved colon , 2000, Gut.

[36]  B. Stoll,et al.  Enteral nutrient intake level determines intestinal protein synthesis and accretion rates in neonatal pigs. , 2000, American journal of physiology. Gastrointestinal and liver physiology.

[37]  J. Holst,et al.  In vivo and in vitro degradation of glucagon-like peptide-2 in humans. , 2000, The Journal of clinical endocrinology and metabolism.

[38]  D. Drucker Glucagon-like Peptide 2 , 1999, Trends in Endocrinology & Metabolism.

[39]  H. Gundersen,et al.  The efficiency of systematic sampling in stereology — reconsidered , 1999, Journal of microscopy.

[40]  P. Mortensen,et al.  Effect of intravenous ranitidine and omeprazole on intestinal absorption of water, sodium, and macronutrients in patients with intestinal resection , 1998, Gut.

[41]  W. MacNaughton,et al.  GLP-2 augments the adaptive response to massive intestinal resection in rat. , 1998, American journal of physiology. Gastrointestinal and liver physiology.

[42]  P. Mortensen,et al.  The influence of a preserved colon on the absorption of medium chain fat in patients with small bowel resection , 1998, Gut.

[43]  D. Drucker,et al.  Induction of intestinal epithelial proliferation by glucagon-like peptide 2. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[44]  A. Fowden,et al.  The Prenatal Development and Glucocorticoid Control of Brush-Border Hydrolases in the Pig Small Intestine , 1995, Pediatric Research.

[45]  N. Qvist,et al.  P313 PRETERM BIRTH REDUCES THE ADAPTATION TO INTESTINAL RESECTION IN NEWBORN PIGS , 2009 .

[46]  J. Holst,et al.  GLP-2 receptor localizes to enteric neurons and endocrine cells expressing vasoactive peptides and mediates increased blood flow. , 2006, Gastroenterology.

[47]  J. Holst,et al.  Glucagon-like peptide 2 dose-dependently activates intestinal cell survival and proliferation in neonatal piglets. , 2005, Endocrinology.

[48]  D. Burrin,et al.  Preterm birth affects the intestinal response to parenteral and enteral nutrition in newborn pigs. , 2002, The Journal of nutrition.

[49]  B. Wise Neonatal short bowel syndrome. , 1992, Neonatal network : NN.