Heparin-binding EGF-like growth factor increases intestinal microvascular blood flow in necrotizing enterocolitis

Gastroenterology. 2009 Jul;137(1):221-30. doi: 10.1053/j.gastro.2009.03.060. Epub 2009 Apr 8.

Abstract

Background & aims: Necrotizing enterocolitis (NEC) is the most common gastrointestinal emergency in neonates. Although the exact etiology remains unknown, decreased intestinal blood flow is believed to play a critical role. We have shown that heparin-binding epidermal growth factor-like growth factor (HB-EGF) protects the intestines from injury in a rodent model of NEC. Our current goal was to assess the effect of HB-EGF on intestinal microvascular blood flow and intestinal injury in rat pups subjected to experimental NEC.

Methods: Newborn rat pups were subjected to stress by exposure to hypoxia, hypothermia, hypertonic feedings, and lipopolysaccharide, with some pups receiving HB-EGF (800 microg x kg(-1) x dose(-1)) added to the feeds. Control animals received breast milk. Intestinal injury was graded using a standard histologic injury scoring system. Microvascular blood flow was assessed by fluorescein isothiocyanate/dextran angiography, with fluorescent images subjected to quantification, and by scanning electron microscopy.

Results: Intestinal microvascular blood flow (defined as the extent of vascular filling with fluorescein isothiocyanate/dextran) was significantly decreased in pups subjected to stress compared with breast-fed pups. Stressed pups treated with HB-EGF had significantly increased microvascular blood flow. The changes in villous microvasculature correlated with histologic injury scores, with stressed pups treated with HB-EGF showing decreased histologic injury.

Conclusions: HB-EGF significantly preserved intestinal microvascular blood flow in pups subjected to experimental NEC, indicating that HB-EGF may play a critical role in the treatment of various diseases manifested by decreased intestinal blood flow, including NEC.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Arterioles / metabolism
  • Arterioles / physiopathology
  • Capillaries / metabolism
  • Capillaries / physiopathology
  • Disease Models, Animal
  • Enterocolitis, Necrotizing / metabolism*
  • Enterocolitis, Necrotizing / pathology
  • Enterocolitis, Necrotizing / physiopathology
  • Enterocolitis, Necrotizing / prevention & control
  • Fluorescein Angiography
  • Heparin-binding EGF-like Growth Factor
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Intestinal Mucosa / blood supply*
  • Intestinal Mucosa / ultrastructure
  • Intestines / blood supply*
  • Intestines / ultrastructure
  • Microcirculation*
  • Microscopy, Confocal
  • Microscopy, Electron, Scanning
  • Microscopy, Fluorescence
  • Microvilli / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Severity of Illness Index
  • Splanchnic Circulation*
  • Venules / metabolism
  • Venules / physiopathology

Substances

  • Hbegf protein, rat
  • Heparin-binding EGF-like Growth Factor
  • Intercellular Signaling Peptides and Proteins