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Review
. 2013 Oct;91(10):4713-29.
doi: 10.2527/jas.2013-6359. Epub 2013 Aug 13.

Invited review: the preterm pig as a model in pediatric gastroenterology

Affiliations
Review

Invited review: the preterm pig as a model in pediatric gastroenterology

P T Sangild et al. J Anim Sci. 2013 Oct.

Abstract

At birth, the newborn mammal undergoes a transition from a sterile uterine environment with a constant nutrient supply, to a microbe-rich environment with intermittent oral intake of complex milk nutrients via the gastrointestinal tract (GIT). These functional challenges partly explain the relatively high morbidity and mortality of neonates. Preterm birth interrupts prenatal organ maturation, including that of the GIT, and increases disease risk. Exemplary is necrotizing enterocolitis (NEC), which is associated closely with GIT immaturity, enteral feeding, and bacterial colonization. Infants with NEC may require resection of the necrotic parts of the intestine, leading to short bowel syndrome (SBS), characterized by reduced digestive capacity, fluid loss, and dependency on parenteral nutrition. This review presents the preterm pig as a translational model in pediatric gastroenterology that has provided new insights into important pediatric diseases such as NEC and SBS. We describe protocols for delivery, care, and handling of preterm pigs, and show how the immature GIT responds to delivery method and different nutritional and therapeutic interventions. The preterm pig may also provide a sensitive model for postnatal adaptation of weak term piglets showing high mortality. Attributes of the preterm pig model include close similarities with preterm infants in body size, organ development, and many clinical features, thereby providing a translational advantage relative to rodent models of GIT immaturity. On the other hand, the need for a sow surgical facility, a piglet intensive care unit, and clinically trained personnel may limit widespread use of preterm pigs. Studies on organ adaptation in preterm pigs help to identify the physiological basis of neonatal survival for hypersensitive newborns and aid in defining the optimal diet and rearing conditions during the critical neonatal period.

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Figures

Figure 1
Figure 1
Maturation (as percentage of gestation) of lungs, gut, and brain relative to term birth, weaning, and total life span for rats, pigs, and humans. Symbols for lungs, gut, and brain indicate the time period when ontogenetic maturation is sufficient to secure general viability of preterm newborns (dark grey boxes), that is, independent breathing (determined by lung alveolar respiration), digestion of nonmilk food (determined by gut functions), and locomotion (in part determined by brain motoric control). See online version for figure in color.
Figure 2
Figure 2
Piglet neonatal intensive care unit. (A–C) Incubator types, room design, and clinical care procedures have been adjusted over the years to improve the care and neonatal adaptation of 20 to 25 preterm piglets per litter. After (B) placement of an orogastric feeding tube and a vascular catheter into a jugular vein or umbilical artery, (C, D) the piglets are placed in heated, ventilated, humidified and oxygenated incubators. (D) Syringe or infusion pumps deliver intravenous or oral nutrition or other therapies. (E) Growth-restricted or normal-weight preterm pigs may also be fed manually by providing intermittent boluses, both before and after they become mobile at 1–5 d after birth. (F) Continuous clinical surveillance is supported by web based cameras. See online version for figure in color.
Figure 3
Figure 3
Flow of events in short-term protocols using preterm pigs delivered by caesarean section at ~90% gestation to investigate factors that prevent necrotizing enterocolitis (NEC, upper panels) or stimulate intestinal adaptation following intestinal resection and short bowel syndrome (SBS, lower panels). See online version for figure in color.

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