Enteral feeding induces early intestinal adaptation in a parenterally fed neonatal piglet model of short bowel syndrome

JPEN J Parenter Enteral Nutr. 2012 Mar;36(2):205-12. doi: 10.1177/0148607111417447. Epub 2011 Dec 21.

Abstract

Background: Successful small intestinal (SI) adaptation following surgical resection is essential for optimizing newborn growth and development, but the potential for adaptation is unknown. The authors developed an SI resection model in neonatal piglets supported by intravenous and enteral nutrition.

Methods: Piglets (n = 33, 12-13 days old) were randomized to 80% SI resection with parenteral nutrition feeding (R-PN), 80% SI resection with PN + enteral feeding (R-EN), or sham SI transection with PN + enteral feeding (sham-EN). In resected pigs, the distal 100 cm of ileum (residual SI) and 30 cm of proximal SI were left intact. All pigs received parenteral nutrition postsurgery. Enteral nutrition piglets received continuous gastric infusion of elemental diet from day 3 (40:60 parenteral nutrition:enteral nutrition). Piglets were killed 4, 6, or 10 days postsurgery.

Results: By 10 days, R-EN piglets had longer residual SI than R-PN and sham-EN pigs (P < .05). At days 6 and 10, R-EN piglets had greater weight per length of intact SI (P < .05) and isolated mucosa (P < .05) compared to other groups. Greater gut weight in R-EN piglets was facilitated by a greater cellular proliferation index (P < .01) by 4 days compared to other groups and greater overall ornithine decarboxylase activity vs R-PN piglets (P < .05).

Conclusions: This new model demonstrated profound SI adaptation, initiated early postsurgery by polyamine synthesis and crypt cell proliferation and only in response to enteral feeding. These changes translated to greater gut mass and length within days, likely improving functional capacity long term.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological*
  • Animals
  • Animals, Newborn
  • Cell Proliferation
  • Disease Models, Animal
  • Enteral Nutrition*
  • Ileum
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / growth & development*
  • Intestine, Small / cytology
  • Intestine, Small / growth & development*
  • Intestine, Small / surgery
  • Organ Size
  • Ornithine Decarboxylase / metabolism
  • Parenteral Nutrition*
  • Random Allocation
  • Short Bowel Syndrome / metabolism
  • Short Bowel Syndrome / surgery
  • Short Bowel Syndrome / therapy*
  • Swine

Substances

  • Ornithine Decarboxylase