Enhanced Ghrelin Levels and Hypothalamic Orexigenic AgRP and NPY Neuropeptide Expression in Models of Jejuno-Colonic Short Bowel Syndrome

Sci Rep. 2016 Jun 21:6:28345. doi: 10.1038/srep28345.

Abstract

Short bowel syndrome (SBS) patients developing hyperphagia have a better outcome. Gastrointestinal endocrine adaptations help to improve intestinal functions and food behaviour. We investigated neuroendocrine adaptations in SBS patients and rat models with jejuno-ileal (IR-JI) or jejuno-colonic (IR-JC) anastomosis with and without parenteral nutrition. Circulating levels of ghrelin, PYY, GLP-1, and GLP-2 were determined in SBS rat models and patients. Levels of mRNA for proglucagon, PYY and for hypothalamic neuropeptides were quantified by qRT-PCR in SBS rat models. Histology and immunostaining for Ki67, GLP-1 and PYY were performed in SBS rats. IR-JC rats, but not IR-JI, exhibited significantly higher crypt depths and number of Ki67-positive cells than sham. Fasting and/or postprandial plasma ghrelin and PYY concentrations were higher, or tend to be higher, in IR-JC rats and SBS-JC patients than in controls. Proglucagon and Pyy mRNA levels were significantly enhanced in IR-JC rats. Levels of mRNA coding hypothalamic orexigenic NPY and AgRP peptides were significantly higher in IR-JC than in sham rats. We demonstrate an increase of plasma ghrelin concentrations, major changes in hypothalamic neuropeptides levels and greater induction of PYY in SBS-JC rats and patients suggesting that jejuno-colonic continuity creates a peculiar environment promoting further gut-brain adaptations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Agouti-Related Protein / metabolism*
  • Anastomosis, Surgical
  • Animals
  • Colon / pathology*
  • Disease Models, Animal
  • Feeding Behavior
  • Female
  • Ghrelin / blood*
  • Glucagon-Like Peptide 1 / blood
  • Glucagon-Like Peptide 2 / blood
  • Humans
  • Hyperphagia / metabolism
  • Hypothalamus / metabolism*
  • Intestinal Mucosa / metabolism
  • Jejunum / pathology*
  • Ki-67 Antigen / metabolism
  • Male
  • Middle Aged
  • Neuropeptide Y / metabolism*
  • Peptide YY / blood
  • Proglucagon / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Real-Time Polymerase Chain Reaction
  • Short Bowel Syndrome / metabolism*

Substances

  • Agouti-Related Protein
  • Ghrelin
  • Glucagon-Like Peptide 2
  • Ki-67 Antigen
  • Neuropeptide Y
  • RNA, Messenger
  • Peptide YY
  • Proglucagon
  • Glucagon-Like Peptide 1