Aims: Intra-uterine growth restriction (IUGR) followed by accelerated postnatal growth is associated with an increased risk of obesity and type 2 diabetes. We aimed to determine central and peripheral insulin sensitivity in mice that underwent IUGR followed by post-natal catch-up growth and investigate potential molecular mechanisms underpinning their physiology. Methods: We used a C57/bl6J mouse model of maternal diet-induced IUGR (maternal diet 8 % protein) followed by cross fostering to a normal nutrition dam (maternal diet 20% protein) and litter size manipulation, to cause accelerated post-natal catch-up growth. We performed intra-cerebroventricular insulin injection and hyperinsulinemic-euglycemic clamps to examine the effect of this ...
These data suggest that insulin secretion in WSB mice is blunted specifically in vivo, either due to...
Caloric restriction (CR) is the only environmental intervention with robust evidence that it extends...
OBJECTIVE: To characterize the hormonal milieu and adipose gene expression in response to catch-up g...
AIMS: Intra-uterine growth restriction (IUGR) followed by accelerated postnatal growth is associated...
BACKGROUND: It is now widely accepted that the early-life nutritional environment is important in de...
12 Pág.Low birth weight and rapid postnatal weight gain are independent predictors of obesity and di...
International audienceINTRODUCTION: Individuals born with intrauterine growth retardation (IUGR) are...
<div><p>Background</p><p>Intrauterine growth restriction (IUGR) and rapid postnatal weight gain or c...
International audienceIncreasing evidence suggests a developmental origin for a number of human dise...
Intrauterine growth restriction (IUGR) and rapid postnatal weight gain or catch up growth (CUG) incr...
Individuals with intrauterine growth retardation (IUGR) are prone to insulin resistance, whereas the...
We previously reported that maternal protein restriction in rodents influenced the rate of growth in...
We previously reported that maternal protein restriction in rodents influenced the rate of growth in...
These data suggest that insulin secretion in WSB mice is blunted specifically in vivo, either due to...
A suboptimal in utero environment leads to fetal adaptations to ensure short-term survival but in th...
These data suggest that insulin secretion in WSB mice is blunted specifically in vivo, either due to...
Caloric restriction (CR) is the only environmental intervention with robust evidence that it extends...
OBJECTIVE: To characterize the hormonal milieu and adipose gene expression in response to catch-up g...
AIMS: Intra-uterine growth restriction (IUGR) followed by accelerated postnatal growth is associated...
BACKGROUND: It is now widely accepted that the early-life nutritional environment is important in de...
12 Pág.Low birth weight and rapid postnatal weight gain are independent predictors of obesity and di...
International audienceINTRODUCTION: Individuals born with intrauterine growth retardation (IUGR) are...
<div><p>Background</p><p>Intrauterine growth restriction (IUGR) and rapid postnatal weight gain or c...
International audienceIncreasing evidence suggests a developmental origin for a number of human dise...
Intrauterine growth restriction (IUGR) and rapid postnatal weight gain or catch up growth (CUG) incr...
Individuals with intrauterine growth retardation (IUGR) are prone to insulin resistance, whereas the...
We previously reported that maternal protein restriction in rodents influenced the rate of growth in...
We previously reported that maternal protein restriction in rodents influenced the rate of growth in...
These data suggest that insulin secretion in WSB mice is blunted specifically in vivo, either due to...
A suboptimal in utero environment leads to fetal adaptations to ensure short-term survival but in th...
These data suggest that insulin secretion in WSB mice is blunted specifically in vivo, either due to...
Caloric restriction (CR) is the only environmental intervention with robust evidence that it extends...
OBJECTIVE: To characterize the hormonal milieu and adipose gene expression in response to catch-up g...