Abstract

Background: Intrauterine growth restriction is a common cause of small for gestational age (SGA) infants worldwide. SGA infants are deficient in digestive enzymes required for fat digestion and absorption compared to appropriate for gestational age (AGA) infants, putting them at risk for impaired neurocognitive development.Objective: The objective was to determine if a hydrolyzed fat (HF) infant formula containing soy free fatty acids, 2-monoacylglycerolpalmitate, cholesterol, and soy lecithin could increase brain tissue incorporation of essential fatty acids or white matter to enhance brain development in SGA and AGA neonatal piglet models.Methods: Sex-matched, littermate pairs of SGA (0.5–0.9 kg) and AGA (1.2–1.8 kg) 2 days old piglets (N = 60) were randomly assigned to control (CON) or HF formula diets in a 2 × 2 factorial design. On day 14, 24 piglets were used for hippocampal RNA-sequencing; the rest began a spatial learning task. On days 26–29, brain structure was assessed by magnetic resonance imaging (MRI). Cerebellum and hippocampus were analyzed for fatty acid content.Results: SGA piglets grew more slowly than AGA piglets, with no effect of diet on daily weight gain or weight at MRI. HF diet did not affect brain weight. HF diet increased relative volumes of 7 brain regions and white matter (WM) volume in both SGA and AGA piglets. However, HF did not ameliorate SGA total WM integrity deficits. RNA sequencing revealed SGA piglets had increased gene expression of synapse and cell signaling pathways and decreased expression of ribosome pathways in the hippocampus compared to AGA. HF decreased expression of immune response related genes in the hippocampus of AGA and SGA piglets, but did not correct gene expression patterns in SGA piglets. Piglets learned the T-maze task at the same rate, but SGA HF, SGA CON, and AGA HF piglets had more accurate performance than AGA CON piglets on reversal day 2. HF increased arachidonic acid (ARA) percentage in the cerebellum and total ARA in the hippocampus.Conclusions: HF enhanced brain development in the neonatal piglet measured by brain volume and WM volume in specific brain regions; however, more studies are needed to assess long-term outcomes.

Highlights

  • Neonatal mortality accounts for 45% of deaths in children under 5 years old worldwide [1], and ∼22% of neonatal deaths in low and middle income countries are small for gestational age (SGA) infants [2]

  • The brain-sparing effect in intrauterine growth restriction (IUGR) infants has been correlated to worse neurodevelopmental outcomes including difficulties with creative problem solving, attention and executive functions, and visuomotor organization [35, 36]

  • Brain to body weight ratios of SGA piglets in this study suggested that the brain-sparing effect had occurred

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Summary

Introduction

Neonatal mortality accounts for 45% of deaths in children under 5 years old worldwide [1], and ∼22% of neonatal deaths in low and middle income countries are small for gestational age (SGA) infants [2]. The cause of SGA birth is often intrauterine growth restriction (IUGR), which leads to complications such as neonatal infections, hypoglycemia, difficulty feeding, and hypothermia [2]. In addition to these immediate problems, SGA infants have an increased risk of delayed neurodevelopment [3]. Many studies have examined the cognitive development and behavior of infants born SGA. A neonatal piglet model of SGA due to IUGR developed by Radlowski et al [7] demonstrated deficits in learning and memory along with white matter (WM) deficits that persisted even with catch up growth. Intrauterine growth restriction is a common cause of small for gestational age (SGA) infants worldwide. SGA infants are deficient in digestive enzymes required for fat digestion and absorption compared to appropriate for gestational age (AGA) infants, putting them at risk for impaired neurocognitive development

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