Abstract

The aim was to test the hypothesis that prenatal under‐ and overnutrition in late gestation can program small intestinal (SI) growth, angiogenesis, and endocrine function to predispose for a hyperabsorptive state, thereby increasing the susceptibility to the adverse effects of an early postnatal obesogenic diet. Twin‐pregnant ewes were exposed to adequate (NORM), LOW (50% of NORM), or HIGH (150% energy and 110% protein of NORM) diets through the last trimester (term ~147 days). From 3 days to 6 months of age, their lambs were fed either a moderate (CONV) or a high‐carbohydrate high‐fat (HCHF) diet. At 6 months of age, responses in plasma metabolites and insulin to refeeding after fasting were determined and then different segments of the SI were sampled at autopsy. Prenatal overnutrition impacts were most abundant in the duodenum where HIGH had increased villus amplification factor and lowered villi thickness with increased IRS‐1 and reduced GH‐R expressions. In jejunum, HIGH lambs had an increased expression of Lactate gene and amplified when exposed to HCHF postnatally. Specifically, in LOW, sensitivity to HCHF was affected in ileum. Thus, the mismatching LOW‐HCHF nutrition increased expressions of angiogenic genes (VEGF, VEGF‐R1, ANGPT1, RTK) and increased mucosa layer (tunica mucosa) thickness but reduced muscle layer (Tunica muscularis) thickness. The SI is a target of prenatal nutritional programming, where late gestation overnutrition increased and shifted digestive capacity for carbohydrates toward the jejunum, whereas late gestation undernutrition predisposed for ileal angiogenesis and carbohydrate and fat hyperabsorptive capacity upon subsequent exposure to postnatal obesogenic diet.

Highlights

  • Numerous studies in humans and different animal models have convincingly demonstrated that adverse prenatal nutrition exposures can impact metabolic and endocrine functions later in life (Barker et al, 1993; Boerschmann, Pflüger, Henneberger, Ziegler, & Hummel, 2010; FabriciusBjerre et al, 2011; Howie, Sloboda, & Vickers, 2012; Meas et al, 2010; Samuelsson et al, 2008)

  • The twin offspring were allocated to one of two different diets fed from 3 days until 6 months of age: an obesogenic, high-carbohydrate, high-fat (HCHF) diet consisting of milk replacer mixed in a 1:1 (v/v) ratio with dairy cream (38% fat in dry matter) and supplemented with rolled maize; or a moderate conventional (CONV) diet consisting of milk replacer and green hay administered in amounts to achieve moderate daily growth rates of 225 g/d

  • The full models for the feeding challenge data included ewe start body weight and body condition score, lamb sex, and birth weight as covariates and the full models for the quantitative real-time PCR (qPCR) data included in addition to these the lamb body weight at 3 months as covariate

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Summary

Introduction

Numerous studies in humans and different animal models have convincingly demonstrated that adverse prenatal nutrition exposures can impact metabolic and endocrine functions later in life (Barker et al, 1993; Boerschmann, Pflüger, Henneberger, Ziegler, & Hummel, 2010; FabriciusBjerre et al, 2011; Howie, Sloboda, & Vickers, 2012; Meas et al, 2010; Samuelsson et al, 2008) This has been ascribed to the phenomenon termed fetal programming. In good correspondence with this, studies of the SI and glucose absorption in diabetic rats have indicated that increased intestinal capacity for glucose absorption can be a contributing factor to diabetes (Adachi et al, 2003; Fujita et al, 1998) These findings made us speculate, whether the SI could be a target of fetal programming and play a role in the predisposition for metabolic disorders such as type 2 diabetes later in life in individuals exposed to fetal malnutrition

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