Glucagon-Like Peptide 2 Stimulates Postresection Intestinal Adaptation in Preterm Pigs by Affecting Proteins Related to Protein, Carbohydrate, and Sulphur Metabolism

JPEN J Parenter Enteral Nutr. 2017 Nov;41(8):1293-1300. doi: 10.1177/0148607116662971. Epub 2016 Aug 8.

Abstract

Background: Exogenous glucagon-like peptide 2 (GLP-2) stimulates intestinal adaptation after resection in animal models of pediatric short bowel syndrome (SBS). It is unknown whether the molecular mechanisms of such GLP-2 effects are similar to those of postresection spontaneous adaptation. Using preterm pigs as a model, we hypothesized that GLP-2 treatment would change the intestinal proteome within the first week after resection, relative to individuals not resected or resected without GLP-2 treatment.

Materials and methods: Two-day-old preterm pigs were subjected to resection of 50% distal small intestine and fed total parenteral nutrition without (SBS) or with GLP-2 infusion (3.5 µg/kg/h, SBS+GLP-2) for 5 days. The proteome of the remnant proximal intestine was compared among the SBS, SBS+GLP-2, and unresected pigs, through gel-based proteomics.

Results: Thirty-two proteins with differential expression were identified. Ten of these proteins were affected by the resection alone (ie, SBS vs unresected pigs). Five of these resection-responsive proteins and another 22 proteins were affected by GLP-2 infusion (ie, SBS+GLP-2 vs SBS or unresected pigs). Resection alone mainly affected cellular structural proteins, while the added GLP-2 treatment affected proteins involved in protein processing and the metabolism of protein, carbohydrate, and sulphur.

Conclusion: In the first days following resection, proteins affected by resection plus GLP-2 treatment differed markedly from those affected by the spontaneous intestinal adaptation following resection alone. Whether more long-term GLP-2 treatment may affect the intestinal proteome following intestinal resection remains unknown.

Keywords: GLP-2; intestinal adaptation; preterm pig; proteomics; research and diseases; short bowel syndrome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological
  • Animals
  • Animals, Newborn
  • Dietary Carbohydrates / metabolism
  • Dietary Proteins / metabolism
  • Disease Models, Animal
  • Glucagon-Like Peptide 2 / pharmacology*
  • Intestine, Small / drug effects*
  • Intestine, Small / metabolism
  • Parenteral Nutrition, Total
  • Short Bowel Syndrome / surgery*
  • Sulfur / metabolism
  • Swine

Substances

  • Dietary Carbohydrates
  • Dietary Proteins
  • Glucagon-Like Peptide 2
  • Sulfur