A. Plagemann, T. Harder, A. Rake, M. Voits, and H. Fink, Perinatal elevation of hypothalamic insulin, acquired malformation of hypothalamic galaninergic neurons, and syndrome X-like alterations in adulthood of neonatally overfed rats, Brain Research, vol.836, issue.1-2, pp.146-155, 1999.
DOI : 10.1016/S0006-8993(99)01662-5

L. Balonan and H. Sheng, Perinatal Feedings Adversely Affect Lipogenic Activities but Not Glucose Handling in Adult Rats, Pediatric Research, vol.264, issue.5, pp.668-673, 2000.
DOI : 10.1203/00006450-200011000-00019

E. Velkoska, T. Cole, and M. Morris, Early dietary intervention: long-term effects on blood pressure, brain neuropeptide Y, and adiposity markers, AJP: Endocrinology and Metabolism, vol.288, issue.6, 2005.
DOI : 10.1152/ajpendo.00505.2004

A. Habbout, S. Delemasure, F. Goirand, J. Guilland, and F. Chabod, Postnatal overfeeding in rats leads to moderate overweight and to cardiometabolic and oxidative alterations in adulthood, Biochimie, vol.94, issue.1, pp.117-124, 2012.
DOI : 10.1016/j.biochi.2011.09.023

L. Kappeler, D. Magalhaes-filho, C. Leneuve, P. Xu, J. Brunel et al., Early Postnatal Nutrition Determines Somatotropic Function in Mice, Endocrinology, vol.150, issue.1, pp.314-323, 2009.
DOI : 10.1210/en.2008-0981

L. Lorgis, M. Zeller, G. Dentan, P. Sicard, and C. Richard, The free oxygen radicals test (FORT) to assess circulating oxidative stress in patients with acute myocardial infarction, Atherosclerosis, vol.213, issue.2, pp.616-621, 2010.
DOI : 10.1016/j.atherosclerosis.2010.09.018

A. Ecarnot-laubriet, R. L. Vergely, C. Sicard, P. Teyssier, and J. , The Activation Pattern of the Antioxidant Enzymes in the Right Ventricle of Rat in Response to Pressure Overload is of Heart Failure Type, Heart Disease, vol.5, issue.5, pp.308-312, 2003.
DOI : 10.1097/01.hdx.0000089836.03515.a9

F. Dalloz, P. Maingon, Y. Cottin, F. Briot, and J. Horiot, Effects of combined irradiation and doxorubicin treatment on cardiac function and antioxidant defenses in the rat, Free Radical Biology and Medicine, vol.26, issue.7-8, pp.785-800, 1999.
DOI : 10.1016/S0891-5849(98)00259-7

H. Aebi, [13] Catalase in vitro, Methods Enzymol, vol.105, pp.121-126, 1984.
DOI : 10.1016/S0076-6879(84)05016-3

N. Suleman, S. Somers, R. Smith, L. Opie, and S. Lecour, Dual activation of STAT-3 and Akt is required during the trigger phase of ischaemic preconditioning, Cardiovascular Research, vol.79, issue.1, pp.127-133, 2008.
DOI : 10.1093/cvr/cvn067

D. Hwang, A. Dempsey, R. Wang, M. Rezvani, and J. Barrans, A Genome-Based Resource for Molecular Cardiovascular Medicine : Toward a Compendium of Cardiovascular Genes, Circulation, vol.96, issue.12, pp.4146-4203, 1997.
DOI : 10.1161/01.CIR.96.12.4146

H. Davidowa and A. Plagemann, Insulin resistance of hypothalamic arcuate neurons in neonatally overfed rats, NeuroReport, vol.18, issue.5, pp.521-524, 2007.
DOI : 10.1097/WNR.0b013e32805dfb93

R. Pereira, A. Moreira, L. De-carvalho, and A. Moura, Overfeeding during lactation modulates insulin and leptin signaling cascade in rats' hearts, Regulatory Peptides, vol.136, issue.1-3, pp.117-121, 2006.
DOI : 10.1016/j.regpep.2006.05.002

S. Boullu-ciocca, A. Dutour, V. Guillaume, V. Achard, and C. Oliver, Postnatal Diet-Induced Obesity in Rats Upregulates Systemic and Adipose Tissue Glucocorticoid Metabolism During Development and in Adulthood: Its Relationship With the Metabolic Syndrome, Diabetes, vol.54, issue.1, pp.197-203, 2005.
DOI : 10.2337/diabetes.54.1.197

A. Cunha, R. Pereira, M. Pereira, S. Vde, M. Martins et al., Long-term effects of overfeeding during lactation on insulin secretion ??? the role of GLUT-2, The Journal of Nutritional Biochemistry, vol.20, issue.6, pp.435-442, 2009.
DOI : 10.1016/j.jnutbio.2008.05.002

M. Lopez, L. Seoane, S. Tovar, M. Garcia, and R. Nogueiras, A possible role of neuropeptide Y, agouti-related protein and leptin receptor isoforms in hypothalamic programming by perinatal feeding in the rat, Diabetologia, vol.44, issue.Suppl 1, pp.140-148, 2005.
DOI : 10.1007/s00125-004-1596-z

S. Rajia, H. Chen, and M. Morris, Maternal overnutrition impacts offspring adiposity and brain appetite markers-modulation by postweaning diet, Journal of Neuroendocrinology, vol.22, pp.905-914, 2010.
DOI : 10.1111/j.1365-2826.2010.02005.x

O. Gualillo, J. Gonzalez-juanatey, and F. Lago, The Emerging Role of Adipokines as Mediators of Cardiovascular Function: Physiologic and Clinical Perspectives, Trends in Cardiovascular Medicine, vol.17, issue.8, pp.275-283, 2007.
DOI : 10.1016/j.tcm.2007.09.005

I. Castan-laurell, C. Dray, C. Attane, T. Duparc, and C. Knauf, Apelin, diabetes, and obesity, Endocrine, vol.96, issue.Suppl 1, pp.1-9, 2011.
DOI : 10.1007/s12020-011-9507-9

URL : https://hal.archives-ouvertes.fr/inserm-00617638

M. Kleinz, J. Skepper, and A. Davenport, Immunocytochemical localisation of the apelin receptor, APJ, to human cardiomyocytes, vascular smooth muscle and endothelial cells, Regulatory Peptides, vol.126, issue.3, pp.233-240, 2005.
DOI : 10.1016/j.regpep.2004.10.019

M. Kleinz and A. Davenport, Immunocytochemical localization of the endogenous vasoactive peptide apelin to human vascular and endocardial endothelial cells, Regulatory Peptides, vol.118, issue.3, pp.119-125, 2004.
DOI : 10.1016/j.regpep.2003.11.002

K. Tatemoto, K. Takayama, M. Zou, I. Kumaki, and W. Zhang, The novel peptide apelin lowers blood pressure via a nitric oxide-dependent mechanism, Regulatory Peptides, vol.99, issue.2-3, pp.87-92, 2001.
DOI : 10.1016/S0167-0115(01)00236-1

M. Berry, T. Pirolli, V. Jayasankar, J. Burdick, and K. Morine, Apelin Has In Vivo Inotropic Effects on Normal and Failing Hearts, Circulation, vol.110, issue.11_suppl_1, pp.187-193, 2004.
DOI : 10.1161/01.CIR.0000138382.57325.5c

I. Scott, B. Masri, D. Amico, L. Jin, S. Jungblut et al., The G Protein-Coupled Receptor Agtrl1b Regulates Early Development of Myocardial Progenitors, Developmental Cell, vol.12, issue.3, pp.403-413, 2007.
DOI : 10.1016/j.devcel.2007.01.012

URL : https://hal.archives-ouvertes.fr/inserm-00504418

D. Laight, K. Desai, N. Gopaul, E. Anggard, and M. Carrier, F2-isoprostane evidence of oxidant stress in the insulin resistant, obese Zucker rat: effects of vitamin E, European Journal of Pharmacology, vol.377, issue.1, pp.89-92, 1999.
DOI : 10.1016/S0014-2999(99)00407-0

A. Oudot, C. Martin, D. Busseuil, C. Vergely, and L. Demaison, NADPH oxidases are in part responsible for increased cardiovascular superoxide production during aging, Free Radical Biology and Medicine, vol.40, issue.12, pp.2214-2222, 2006.
DOI : 10.1016/j.freeradbiomed.2006.02.020

H. Vincent, S. Powers, D. Stewart, R. Shanely, and H. Demirel, Obesity is associated with increased myocardial oxidative stress, International Journal of Obesity, vol.23, issue.1, pp.67-74, 1999.
DOI : 10.1038/sj.ijo.0800761

Y. Abe, K. Ono, T. Kawamura, H. Wada, and T. Kita, Leptin induces elongation of cardiac myocytes and causes eccentric left ventricular dilatation with compensation, American Journal of Physiology - Heart and Circulatory Physiology, vol.292, issue.5, pp.2387-2396, 2007.
DOI : 10.1152/ajpheart.00579.2006

L. Perego, P. Pizzocri, D. Corradi, F. Maisano, and M. Paganelli, Circulating Leptin Correlates with Left Ventricular Mass in Morbid (Grade III) Obesity before and after Weight Loss Induced by Bariatric Surgery: A Potential Role for Leptin in Mediating Human Left Ventricular Hypertrophy, The Journal of Clinical Endocrinology & Metabolism, vol.90, issue.7, pp.4087-4093, 2005.
DOI : 10.1210/jc.2004-1963

P. Schulze, J. Kratzsch, A. Linke, N. Schoene, and V. Adams, Elevated serum levels of leptin and soluble leptin receptor in patients with advanced chronic heart failure, European Journal of Heart Failure, vol.76, issue.2-3, pp.33-40, 2003.
DOI : 10.1016/S1388-9842(02)00177-0

C. Vergely, A. Tabard, V. Maupoil, and R. L. , -butylnitrone, Free Radical Research, vol.24, issue.5, pp.475-489, 2001.
DOI : 10.1271/bbb.62.275

URL : https://hal.archives-ouvertes.fr/halshs-00480471

K. Boengler, D. Hilfiker-kleiner, H. Drexler, G. Heusch, and R. Schulz, The myocardial JAK/STAT pathway: From protection to failure, Pharmacology & Therapeutics, vol.120, issue.2, pp.172-185, 2008.
DOI : 10.1016/j.pharmthera.2008.08.002

B. Fuglesteg, N. Suleman, C. Tiron, T. Kanhema, and L. Lacerda, Signal transducer and activator of transcription 3 is involved in the cardioprotective signalling pathway activated by insulin therapy at reperfusion, Basic Research in Cardiology, vol.275, issue.5, pp.444-453, 2008.
DOI : 10.1007/s00395-008-0728-x

R. Hattori, N. Maulik, H. Otani, L. Zhu, and G. Cordis, Role of STAT3 in Ischemic Preconditioning, Journal of Molecular and Cellular Cardiology, vol.33, issue.11, pp.1929-1936, 2001.
DOI : 10.1006/jmcc.2001.1456

R. Kelly, K. Lamont, S. Somers, D. Hacking, and L. Lacerda, Ethanolamine is a novel STAT-3 dependent cardioprotective agent, Basic Research in Cardiology, vol.338, issue.Pt 3, pp.763-770, 2010.
DOI : 10.1007/s00395-010-0125-0

M. Alcazar, E. Boehler, E. Rother, K. Amann, and C. Vohlen, Early Postnatal Hyperalimentation Impairs Renal Function via SOCS-3 Mediated Renal Postreceptor Leptin Resistance, Endocrinology, vol.153, issue.3, pp.1397-1410, 2012.
DOI : 10.1210/en.2011-1670