Enteral nutrient deprivation in patients leads to a loss of intestinal epithelial barrier function

Surgery. 2015 Apr;157(4):732-42. doi: 10.1016/j.surg.2014.12.004. Epub 2015 Feb 20.

Abstract

Objective: To investigate the effect of nutrient withdrawal on human intestinal epithelial barrier function (EBF). We hypothesized that unfed mucosa results in decreased EBF. This was tested in a series of surgical small intestinal resection specimens.

Design: Small bowel specifically excluding inflamed tissue, was obtained from pediatric patients (aged 2 days to 19 years) undergoing intestinal resection. EBF was assessed in Ussing chambers for transepithelial resistance (TER) and passage of fluorescein isothiocyanate (FITC)-dextran (4 kD). Tight junction and adherence junction proteins were imaged with immunofluorescence staining. Expression of Toll-like receptors (TLR) and inflammatory cytokines were measured in loop ileostomy takedowns in a second group of patients.

Results: Because TER increased with patient age (P < .01), results were stratified into infant versus teenage groups. Fed bowel had significantly greater TER versus unfed bowel (P < .05) in both age populations. Loss of EBF was also observed by an increase in FITC-dextran permeation in enteral nutrient-deprived segments (P < .05). Immunofluorescence staining showed marked declines in intensity of ZO-1, occludin, E-cadherin, and claudin-4 in unfed intestinal segments, as well as a loss of structural formation of tight junctions. Analysis of cytokine and TLR expression showed significant increases in tumor necrosis factor (TNF)-α and TLR4 in unfed segments of bowel compared with fed segments from the same individual.

Conclusion: EBF declined in unfed segments of human small bowel. This work represents the first direct examination of EBF from small bowel derived from nutrient-deprived humans and may explain the increased incidence of infectious complications seen in patients not receiving enteral feeds.

Publication types

  • Evaluation Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adherens Junctions / metabolism*
  • Adolescent
  • Biomarkers / metabolism
  • Child
  • Child, Preschool
  • Cytokines / metabolism
  • Enteral Nutrition*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / physiopathology*
  • Intestine, Small / metabolism
  • Intestine, Small / physiopathology*
  • Linear Models
  • Male
  • Parenteral Nutrition / adverse effects*
  • Permeability
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tight Junctions / metabolism*
  • Toll-Like Receptors / metabolism
  • Young Adult

Substances

  • Biomarkers
  • Cytokines
  • Toll-Like Receptors