Abstract

Nutritional environment in the perinatal period has a great influence on health and diseases in adulthood. In rodents, litter size reduction reproduces the effects of postnatal overnutrition in infants and reveals that postnatal overfeeding (PNOF) not only permanently increases body weight but also affects the cardiovascular function in the short- and long-term. In addition to increased adiposity, the metabolic status of PNOF rodents is altered, with increased plasma insulin and leptin levels, associated with resistance to these hormones, changed profiles and levels of circulating lipids. PNOF animals present elevated arterial blood pressure with altered vascular responsiveness to vasoactive substances. The hearts of overfed rodents exhibit hypertrophy and elevated collagen content. PNOF also induces a disturbance of cardiac mitochondrial respiration and produces an imbalance between oxidants and antioxidants. A modification of the expression of crucial genes and epigenetic alterations is reported in hearts of PNOF animals. In vivo, a decreased ventricular contractile function is observed during adulthood in PNOF hearts. All these alterations ultimately lead to an increased sensitivity to cardiac pathologic challenges such as ischemia-reperfusion injury. Nevertheless, caloric restriction and physical exercise were shown to improve PNOF-induced cardiac dysfunction and metabolic abnormalities, drawing a path to the potential therapeutic correction of early nutritional programming.

Highlights

  • Growth trajectories [1] are essential to determine maturity metabolism and health in adulthood

  • As observed earlier by Plagemann [39,40,41,42], rodents subjected to postnatal overfeeding (PNOF) have a significantly higher body weight than controls at weaning, which persists through growth and maturation

  • Early changes in circulating lipids or other metabolic substrate levels observed in PNOF animals may directly impact cardiomyocytes’ ability to proliferate in the immediate postnatal period and could have a long-term impact on cardiac hypertrophy and myocardial susceptibility to pathological stressors

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Summary

Introduction

Growth trajectories [1] are essential to determine maturity metabolism and health in adulthood. Foetal exposure to toxic components, endocrine disruptors and to under- or over-nutrition are key determinants in the development of metabolic diseases later in life and are all related to the concept of developmental programming [2]. This theory suggests that hormonal or nutritional factors in the neonatal period can lead to major changes in gene expression, initially intended to adapt the organism to changes in its environment. Cardiac hypertrophy ↑ susceptibility to ex vivo ischemia-reperfusion Alteration of insulin and fatty acid pathways [E]: ↑ plasma glucose/insulin/triglycerides/total cholesterol levels Alteration of cardiac insulin pathways Cardiac hypertrophy and fibrosis Alteration of cardiac metabolism [29]

PNOF is Associated with Systemic and Cardiovascular Metabolic Alterations
PNOF Affects Blood Pressure and Vascular Function
PNOF Impairs the Architecture and Structure of the Heart
PNOF Induces Short- and Long-Term Alterations of Gene Expression in the Heart
PNOF Alters Cardiac Function In Vivo
PNOF Increases Myocardial Susceptibility to Pathological Stresses
Openings
Findings
Conclusions
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