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Published on: June 27, 2014
Hypothalamic neuropeptide expression of juvenile and middle-aged rats after early postnatal food restriction
Floor Remmers1, Linda A W Verhagen, Roger A H Adan
1Department of Pediatrics, Vrije Universiteit University Medical Center, Amsterdam, The Netherlands. floorremmers@hotmail.com
Insights
Early postnatal food restriction (FR) in rats persistently alters energy balance by reprogramming hypothalamic gene expression, leading to a lower body weight set-point. This programming affects key neuropeptides involved in appetite regulation from a young age.
Area of Science:
- Neuroscience
- Endocrinology
- Developmental Biology
Background:
- Early life nutrition significantly impacts long-term energy balance and metabolic health.
- The hypothalamus is a critical brain region regulating appetite and body weight.
- Developmental programming can alter physiological systems in response to early environmental cues.
Purpose of the Study:
- To investigate the long-term effects of early postnatal food restriction (FR) on hypothalamic neuropeptide gene expression in rats.
- To determine if FR induces developmental programming of appetite-regulating neuropeptides.
- To assess changes in gene expression in specific hypothalamic nuclei (ARC, PVN, LHA) at juvenile and middle-aged stages.
Main Methods:
- Rats were raised in litters with either normal (10 pups) or restricted (20 pups) feeding conditions.
- Gene expression of key neuropeptides (NPY, AgRP, POMC, CART, CRH, TRH, MCH, orexin) was analyzed in hypothalamic regions.
- Analysis was performed on samples from juvenile and middle-aged rats subjected to early FR.
Main Results:
- Early FR led to persistent reductions in body size.
- Juvenile FR rats showed decreased CART and increased MCH gene expression.
- Middle-aged FR rats exhibited reduced POMC and CART mRNA levels.
- The ratio of orexigenic to anorexigenic peptides in the ARC was elevated in juvenile FR rats.
Conclusions:
- Early postnatal food restriction programs hypothalamic neuropeptide expression, favoring orexigenic over anorexigenic signals.
- This programming affects the arcuate nucleus (ARC) and lateral hypothalamic area (LHA), but not the paraventricular nucleus (PVN).
- Adult FR rats appear to adapt to a lower body weight set-point, suggesting successful developmental programming.
Abstract:
Rats subjected to early postnatal food restriction (FR) show persistent changes in energy balance. The hypothalamus plays a major role in the regulation of energy balance. Therefore, we hypothesized that early postnatal food restriction induces developmental programming of hypothalamic gene expression of neuropeptides involved in this regulation. In the hypothalamus of juvenile and middle-aged rats that were raised in control (10 pups) or FR litters (20 pups), gene expression was investigated for neuropeptide Y (NPY), agouti-related protein (AgRP), proopiomelanocortin (POMC), and cocaine- and amphetamine-regulated transcript (CART) in the arcuate nucleus (ARC); CRH and TRH in the paraventricular nucleus; and melanin-concentrating hormone (MCH) and orexin in the lateral hypothalamic area. Early postnatal FR acutely and persistently reduced body size. Juvenile FR rats had significantly reduced CART gene expression and increased MCH expression. In middle-aged FR rats, POMC and CART mRNA levels were significantly reduced. The ratio between expression of the ARC orexigenic peptides (NPY and AgRP) and anorexigenic peptides (POMC and CART) was increased in juvenile, but not in middle-aged, FR rats. These results suggest that in neonatal rats, FR already triggers the ARC, and to a lesser extent the lateral hypothalamic area, but not the paraventricular nucleus, to increase expression of orexigenic relative to anorexigenic peptides. In addition, with enduring small body size and normalized hypothalamic gene expression, the adult FR rats appeared to have accepted this smaller body size as normal. This suggests that the body weight set-point was differently programmed in animals with early postnatal FR.
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