Oral administration of surfactant protein-a reduces pathology in an experimental model of necrotizing enterocolitis

J Pediatr Gastroenterol Nutr. 2015 May;60(5):613-20. doi: 10.1097/MPG.0000000000000678.

Abstract

Objectives: Necrotizing enterocolitis (NEC) frequently results in significant morbidity and mortality in premature infants. Others reported that mice deficient in pulmonary surfactant protein-A (SP-A) born and raised in a nonhygienic environment succumb to significant gastrointestinal tract pathology, and enteral administration of purified SP-A significantly reduced mortality. We hypothesized that oral administration of purified SP-A can ameliorate pathology in an experimental model of neonatal NEC.

Methods: Experimental NEC was induced in newborn Sprague-Dawley rat pups by daily formula gavage and intermittent exposure to hypoxia. Purified human SP-A (5 μg/day) was administered by oral gavage. After 4 days, surviving pups were sacrificed, and intestinal pathology was assessed by histological examination of distal terminal ileal sections. Intestinal levels of inflammatory cytokines (IL-1β, IFN-γ, and TNF-α) were assessed by enzyme-linked immunosorbent assay and levels of Toll-like receptor 4 (TLR4) by Western analysis.

Results: Sixty-one percent of the gavaged rat pups that survived to day 4 met the criteria for experimental NEC after hypoxia, whereas treatment with SP-A significantly reduced mortality and assessment of NEC. Intestinal levels of proinflammatory cytokines were significantly increased in pups exposed to hypoxia. Administration of SP-A to pups exposed to hypoxia significantly reduced IL-1β and TNF-α levels, but had little effect on elevated levels of IFN-γ. SP-A treatment of hypoxia-exposed pups significantly reduced expression of intestinal TLR4, key in NEC pathogenesis.

Conclusions: In a rat model of experimental neonatal NEC, oral administration of SP-A reduces intestinal levels of proinflammatory cytokines and TLR4 protein and ameliorates adverse outcomes associated with gastrointestinal pathologies.

Publication types

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

MeSH terms

  • Administration, Oral
  • Animals
  • Cytokines / metabolism*
  • Disease Models, Animal
  • Enterocolitis, Necrotizing / drug therapy*
  • Enterocolitis, Necrotizing / metabolism
  • Enterocolitis, Necrotizing / pathology
  • Ileum / metabolism
  • Interferon-gamma / metabolism
  • Interleukin-1beta / metabolism
  • Pulmonary Surfactant-Associated Protein A / administration & dosage*
  • Pulmonary Surfactants / administration & dosage*
  • Rats
  • Rats, Sprague-Dawley
  • Toll-Like Receptor 4 / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cytokines
  • Interleukin-1beta
  • Pulmonary Surfactant-Associated Protein A
  • Pulmonary Surfactants
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma