Abstract

BackgroundEarly postnatal environments may have long-term and potentially irreversible consequences on hypothalamic neurons involved in energy homeostasis. Litter size is an important life history trait and negatively correlated with milk intake in small mammals, and thus has been regarded as a naturally varying feature of the early developmental environment. Here we investigated the long-term effects of litter size on metabolic phenotype and hypothalamic neuropeptide mRNA expression involved in the regulation of energy homeostasis, using the offspring reared from large (10–12) and small (3–4) litter sizes, of Brandt's voles (Lasiopodomys brandtii), a rodent species from Inner Mongolia grassland in China.Methodology/Principal FindingsHypothalamic leptin signaling and neuropeptides were measured by Real-Time PCR. We showed that offspring reared from small litters were heavier at weaning and also in adulthood than offspring from large litters, accompanied by increased food intake during development. There were no significant differences in serum leptin levels or leptin receptor (OB-Rb) mRNA in the hypothalamus at weaning or in adulthood, however, hypothalamic suppressor of cytokine signaling 3 (SOCS3) mRNA in adulthood increased in small litters compared to that in large litters. As a result, the agouti-related peptide (AgRP) mRNA increased in the offspring from small litters.Conclusions/SignificanceThese findings support our hypothesis that natural litter size has a permanent effect on offspring metabolic phenotype and hypothalamic neuropeptide expression, and suggest central leptin resistance and the resultant increase in AgRP expression may be a fundamental mechanism underlying hyperphagia and the increased risk of overweight in pups of small litters. Thus, we conclude that litter size may be an important and central determinant of metabolic fitness in adulthood.

Highlights

  • Early-life environmental influences on the adult metabolic phenotype are of interest both scientifically and clinically, as it relates to the risk factors contributing to the obesity epidemic [1]

  • We investigated the long-term effects of natural litter sizes on offspring metabolic phenotype and biomarkers, such as food intake, resting metabolic rate (RMR), nonshivering thermogenesis (NST), uncoupling protein 1 (UCP1) in brown adipose tissue (BAT), body compositions, serum leptin and tri-iodothyronine (T3) and thyroxine (T4) levels in adulthood

  • We used a wild rodent model to examine the consequences of postnatal litter size on offspring growth and adult metabolic phenotype, and to investigate the central mechanisms contributing to the long-term effect of litter size on metabolic fitness

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Summary

Introduction

Early-life environmental influences on the adult metabolic phenotype are of interest both scientifically and clinically, as it relates to the risk factors contributing to the obesity epidemic [1]. Adult rats [4,5] and mice [6,7] previously subjected to early postnatal overnutrition in small litters are hyperphagic, hyperleptinemic and differ in emotional behavior from control litters. These observations from either maternal high-fat diet or litter size manipulation underscore the critical importance of early postnatal nutritional environment in ‘‘programming’’ the long-term regulation of energy homeostasis [8,9]. We investigated the long-term effects of litter size on metabolic phenotype and hypothalamic neuropeptide mRNA expression involved in the regulation of energy homeostasis, using the offspring reared from large (10–12) and small (3–4) litter sizes, of Brandt’s voles (Lasiopodomys brandtii), a rodent species from Inner Mongolia grassland in China

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