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1.
Proc Nutr Soc ; 69(2): 221-31, 2010 May.
Article in English | MEDLINE | ID: mdl-20202279

ABSTRACT

The phenotype of an individual is the result of complex interactions between genome, epigenome and current, past and ancestral environment leading to a lifelong remodelling of the epigenomes. The genetic information expression contained in the genome is controlled by labile chromatin-associated epigenetic marks. Epigenetic misprogramming during development is widely thought to have a persistent effect on the health of the offspring and may even be transmitted to the next generation. The epigenome serves as an interface between the environment and the genome. Dietary factors, including folate involved in C1 metabolism, and other social and lifestyle exposures have a profound effect on many aspects of health including ageing and do so, at least partly, through interactions with the genome, which result in altered gene expression with consequences for cell function and health throughout the life course. Depending on the nature and intensity of the environmental insult, the critical spatiotemporal windows and developmental or lifelong processes involved, epigenetic alterations can lead to permanent changes in tissue and organ structure and function or to phenotypic changes that can (or cannot) be reversed using appropriate epigenetic tools. Moreover, the flexibility of epigenetic marks may make it possible for environmental, nutritional and hormonal factors or endocrine disruptors to alter, during a particular spatiotemporal window in a sex-specific manner, the sex-specific methylation or demethylation of specific CpG and/or histone modifications underlying sex-specific expression of a substantial proportion of genes. Moreover, genetic factors, the environment and stochastic events change the epigenetic landscape during the lifetime of an individual. Epigenetic alterations leading to gene expression dysregulation accumulate during ageing and are important in tumorigenesis and age-related diseases. Several encouraging trials suggest that prevention and therapy of age- and lifestyle-related diseases by individualised tailoring to optimal epigenetic diets or drugs are conceivable. However, these interventions will require intense efforts to unravel the complexity of these epigenetic, genetic and environment interactions and to evaluate their potential reversibility with minimal side effects.


Subject(s)
Diet , Epigenesis, Genetic , Gene Expression Regulation, Developmental , Metabolic Diseases/genetics , Nutrigenomics , Animals , Female , Humans , Male , Mice , Pregnancy , Rats
2.
J Physiol Pharmacol ; 59 Suppl 1: 55-63, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18802216

ABSTRACT

The incidence of obesity is rapidly increasing all over the world in epidemic proportions.The epidemia now affects young children and accumulative evidences suggest that the origin of the disease may occur during foetal development and early life. This has introduced the concept of "developmental programming" supported by experimental studies in animal models and numerous epidemiological data. This concept supports the idea that nutritional and hormonal status during pregnancy and early life could interfere irreversibly on the development of the organs involved in the control of food intake and metabolism and particularly the hypothalamic structures responsible of the establishment of the ingestive behaviour and regulation of energy expenditure. The mechanisms responsible of this developmental programming remain poorly documented. However, recent research indicate that the adipokine leptin plays a critical role in this programming.


Subject(s)
Genomic Imprinting , Leptin/physiology , Obesity/metabolism , Animals , Eating , Female , Fetal Growth Retardation/genetics , Fetal Growth Retardation/metabolism , Humans , Obesity/embryology , Obesity/genetics , Pregnancy , Risk Factors
3.
Am J Physiol Endocrinol Metab ; 295(5): E1117-25, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18780769

ABSTRACT

Low birth weight resulting from intrauterine growth retardation (IUGR) is a risk factor for further development of metabolic diseases. The pig appears to reproduce nearly all of the phenotypic pathological consequences of human IUGR and is likely to be more relevant than rodents in studies of neonatal development. In the present work, we characterized the model of low-birth-weight piglets with particular attention to the hypothalamic leptin-sensitive system, and we tested whether postnatal leptin supplementation can reverse the precocious signs of adverse metabolic programming. Our results demonstrated that 1) IUGR piglets present altered postnatal growth and increased adiposity; 2) IUGR piglets exhibit abnormal hypothalamic distribution of leptin receptors that may be linked to further disturbance in food-intake behavior; and 3) postnatal leptin administration can partially reverse the IUGR phenotype by correcting growth rate, body composition, and development of several organs involved in metabolic regulation. We conclude that IUGR may be characterized by altered leptin receptor distribution within the hypothalamic structures involved in metabolic regulation and that leptin supplementation can partially reverse the IUGR phenotype. These results open interesting therapeutic perspectives in physiopathology for the correction of defects observed in IUGR.


Subject(s)
Fetal Growth Retardation/metabolism , Hypothalamus/metabolism , Leptin/pharmacology , Receptors, Leptin/genetics , Sus scrofa/metabolism , Adipocytes, White/cytology , Adipocytes, White/drug effects , Adipocytes, White/metabolism , Adipose Tissue, White/drug effects , Adipose Tissue, White/growth & development , Adipose Tissue, White/metabolism , Animals , Animals, Newborn , Birth Weight/drug effects , Blood Glucose/metabolism , Body Composition/drug effects , Body Composition/physiology , Body Size/drug effects , Body Weight/drug effects , Female , Fetal Growth Retardation/blood , Fetal Growth Retardation/drug therapy , Gene Expression/drug effects , In Situ Hybridization , Leptin/blood , Leptin/therapeutic use , Sus scrofa/growth & development , Triglycerides/blood , Weight Gain/drug effects
4.
Int J Obes (Lond) ; 32(7): 1153-60, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18379577

ABSTRACT

OBJECTIVE: Using a recombinant rat leptin antagonist, we investigated the effects of early postnatal leptin disruption on long-term leptin sensitivity and metabolic phenotype. DESIGN: Three groups of 10 newborn female Wistar rats were injected subcutaneously with either saline (control) or leptin antagonist (at 2.5 or 7.5 microg g(-1) day(-1)) from postnatal day 2 to day 13. RESULTS: At weaning (day 28), antagonist-treated rats presented similar body weight (BW) compared to control animals. At 3 months of age, there was no significant change in BW, food intake and leptin or insulin levels between groups. Only a disturbed relationship between circulating insulin and glucose levels was observed in antagonist-treated animals. At 4 months of age, treated animals developed a leptin resistance appreciated by the lack of response to a 7-days leptin treatment (1 mg kg(-1) day(-1)) in term of decrease in food intake and BW. At 8 months of age, following 3 months of high-energy diet, rlepm7.5 animals presented higher BW gain associated with increased body fatness and striking hyperleptinaemia as compared to control animals. CONCLUSION: The blockage of leptin action during the critical period of early life in rodents has long-term consequences by altering the capacity to respond to leptin during adulthood, thus predisposing the animals to obesity. These findings clearly demonstrate the physiological importance of the postnatal leptin surge for the optimal onset of the metabolic regulation, at least in rodents, and its implication in the prevention of unfavourable developmental programming.


Subject(s)
Leptin/antagonists & inhibitors , Obesity/metabolism , Animals , Animals, Newborn , Body Weight , Disease Susceptibility , Eating , Female , Insulin/blood , Leptin/blood , Rats , Rats, Wistar , Recombinant Proteins/administration & dosage , Time , Weaning
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