Postnatal growth after intrauterine growth restriction alters central leptin signal and energy homeostasis.

Intrauterine growth restriction (IUGR) is closely linked with metabolic diseases, appetite disorders and obesity at adulthood. Leptin, a major adipokine secreted by adipose tissue, circulates in direct proportion to body fat stores, enters the brain and regulates food intake and energy expenditure....

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Main Authors: Bérengère Coupé, Isabelle Grit, Philippe Hulin, Gwenaëlle Randuineau, Patricia Parnet
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3264579?pdf=render
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spelling doaj-63f3512f522d4c8ea10f847e1da7dc672020-11-25T02:00:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0171e3061610.1371/journal.pone.0030616Postnatal growth after intrauterine growth restriction alters central leptin signal and energy homeostasis.Bérengère CoupéIsabelle GritPhilippe HulinGwenaëlle RanduineauPatricia ParnetIntrauterine growth restriction (IUGR) is closely linked with metabolic diseases, appetite disorders and obesity at adulthood. Leptin, a major adipokine secreted by adipose tissue, circulates in direct proportion to body fat stores, enters the brain and regulates food intake and energy expenditure. Deficient leptin neuronal signalling favours weight gain by affecting central homeostatic circuitry. The aim of this study was to determine if leptin resistance was programmed by perinatal nutritional environment and to decipher potential cellular mechanisms underneath.We clearly demonstrated that 5 months old IUGR rats develop a decrease of leptin sentivity, characterized by no significant reduction of food intake following an intraperitoneal injection of leptin. Apart from the resistance to leptin injection, results obtained from IUGR rats submitted to rapid catch-up growth differed from those of IUGR rats with no catch-up since we observed, for the first group only, fat accumulation, increased appetite for food rich in fat and increased leptin synthesis. Centrally, the leptin resistant state of both groups was associated with a complex and not always similar changes in leptin receptor signalling steps. Leptin resistance in IUGR rats submitted to rapid catch-up was associated with alteration in AKT and mTOR pathways. Alternatively, in IUGR rats with no catch-up, leptin resistance was associated with low hypothalamic expression of LepRa and LepRb. This study reveals leptin resistance as an early marker of metabolic disorders that appears before any evidence of body weight increase in IUGR rats but whose mechanisms could depend of nutritional environment of the perinatal period.http://europepmc.org/articles/PMC3264579?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Bérengère Coupé
Isabelle Grit
Philippe Hulin
Gwenaëlle Randuineau
Patricia Parnet
spellingShingle Bérengère Coupé
Isabelle Grit
Philippe Hulin
Gwenaëlle Randuineau
Patricia Parnet
Postnatal growth after intrauterine growth restriction alters central leptin signal and energy homeostasis.
PLoS ONE
author_facet Bérengère Coupé
Isabelle Grit
Philippe Hulin
Gwenaëlle Randuineau
Patricia Parnet
author_sort Bérengère Coupé
title Postnatal growth after intrauterine growth restriction alters central leptin signal and energy homeostasis.
title_short Postnatal growth after intrauterine growth restriction alters central leptin signal and energy homeostasis.
title_full Postnatal growth after intrauterine growth restriction alters central leptin signal and energy homeostasis.
title_fullStr Postnatal growth after intrauterine growth restriction alters central leptin signal and energy homeostasis.
title_full_unstemmed Postnatal growth after intrauterine growth restriction alters central leptin signal and energy homeostasis.
title_sort postnatal growth after intrauterine growth restriction alters central leptin signal and energy homeostasis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Intrauterine growth restriction (IUGR) is closely linked with metabolic diseases, appetite disorders and obesity at adulthood. Leptin, a major adipokine secreted by adipose tissue, circulates in direct proportion to body fat stores, enters the brain and regulates food intake and energy expenditure. Deficient leptin neuronal signalling favours weight gain by affecting central homeostatic circuitry. The aim of this study was to determine if leptin resistance was programmed by perinatal nutritional environment and to decipher potential cellular mechanisms underneath.We clearly demonstrated that 5 months old IUGR rats develop a decrease of leptin sentivity, characterized by no significant reduction of food intake following an intraperitoneal injection of leptin. Apart from the resistance to leptin injection, results obtained from IUGR rats submitted to rapid catch-up growth differed from those of IUGR rats with no catch-up since we observed, for the first group only, fat accumulation, increased appetite for food rich in fat and increased leptin synthesis. Centrally, the leptin resistant state of both groups was associated with a complex and not always similar changes in leptin receptor signalling steps. Leptin resistance in IUGR rats submitted to rapid catch-up was associated with alteration in AKT and mTOR pathways. Alternatively, in IUGR rats with no catch-up, leptin resistance was associated with low hypothalamic expression of LepRa and LepRb. This study reveals leptin resistance as an early marker of metabolic disorders that appears before any evidence of body weight increase in IUGR rats but whose mechanisms could depend of nutritional environment of the perinatal period.
url http://europepmc.org/articles/PMC3264579?pdf=render
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