Infant digestion physiology and the relevance of in vitro biochemical models to test infant formula lipid digestion

Mol Nutr Food Res. 2016 Aug;60(8):1876-95. doi: 10.1002/mnfr.201500883.

Abstract

Lipids play an important role in the diet of preterm and term infants providing a key energy source and essential lipid components for development. While a lot is known about adult lipid digestion, our understanding of infant digestion physiology is still incomplete, the greatest gap being on the biochemistry of the small intestine, particularly the activity and relative importance of the various lipases active in the intestine. The literature has been reviewed to identify the characteristics of lipid digestion of preterm and term infants, but also to better understand the physiology of the infant gastrointestinal tract compared to adults that impacts the absorption of lipids. The main differences are a higher gastric pH, submicellar bile salt concentration, a far more important role of gastric lipases as well as differences at the level of the intestinal barrier. Importantly, the consequences of improper in vitro replication of gastric digestions conditions (pH and lipase specificity) are demonstrated using examples from the most recent of studies. It is true that some animal models could be adapted to study infant lipid digestion physiology, however the ethical relevance of such models is questionable, hence the development of accurate in vitro models is a must. In vitro models that combine up to date knowledge of digestion biochemistry with intestinal cells in culture are the best choice to replicate digestion and absorption in infant population, this would allow the adaptation of infant formula for a better digestion and absorption of dietary lipids by preterm and term infants.

Keywords: Digestion; Digestion models; Infant; Lipid; Malabsorption.

Publication types

  • Review

MeSH terms

  • Digestion / physiology*
  • Gastrointestinal Tract / metabolism
  • Humans
  • Infant Formula*
  • Infant, Newborn
  • Lipid Metabolism / physiology
  • Models, Biological