S. Ferguson, K. Delclos, R. Newbold, and K. Flynn, Dietary ethinyl estradiol exposure during development causes increased voluntary sodium intake and mild maternal and offspring toxicity in rats, Neurotoxicology and Teratology, vol.25, issue.4, pp.491-501, 2003.
DOI : 10.1016/S0892-0362(03)00015-1

N. Geary and . Estradiol, Estradiol, CCK and satiation, Peptides, vol.22, issue.8, pp.1251-63, 2001.
DOI : 10.1016/S0196-9781(01)00449-1

K. Curtis, L. Davis, A. Johnson, K. Therrien, and R. Contreras, Sex differences in behavioral taste responses to and ingestion of sucrose and NaCl solutions by rats, Physiology & Behavior, vol.80, issue.5, pp.657-64, 2004.
DOI : 10.1016/j.physbeh.2003.11.007

M. Symonds, A. Mostyn, S. Pearce, H. Budge, and T. Stephenson, Endocrine and nutritional regulation of fetal adipose tissue development, Journal of Endocrinology, vol.179, issue.3, pp.293-302, 2003.
DOI : 10.1677/joe.0.1790293

URL : http://joe.endocrinology-journals.org/content/179/3/293.full.pdf

K. Kawai, K. Sugimoto, K. Nakashima, H. Miura, and Y. Ninomiya, Leptin as a modulator of sweet taste sensitivities in mice, Proceedings of the National Academy of Sciences, vol.76, issue.3, pp.11044-11053, 2000.
DOI : 10.1113/jphysiol.1996.sp021147

M. Rocha, C. Bing, G. Williams, and M. Puerta, Physiologic estradiol levels enhance hypothalamic expression of the long form of the leptin receptor in intact rats, The Journal of Nutritional Biochemistry, vol.15, issue.6, pp.328-362, 2004.
DOI : 10.1016/j.jnutbio.2004.01.003

S. Boudalia, R. Berges, C. Chabanet, M. Folia, L. Decocq et al., A multi-generational study on low-dose BPA exposure in Wistar rats: Effects on maternal behavior, flavor intake and development, Neurotoxicology and Teratology, vol.41, pp.16-26, 2014.
DOI : 10.1016/j.ntt.2013.11.002

URL : https://hal.archives-ouvertes.fr/hal-01213723

J. Miyawaki, K. Sakayama, H. Kato, H. Yamamoto, and H. Masuno, Perinatal and Postnatal Exposure to Bisphenol A Increases Adipose Tissue Mass and Serum Cholesterol Level in Mice, Journal of Atherosclerosis and Thrombosis, vol.14, issue.5, pp.245-52, 2007.
DOI : 10.5551/jat.E486

R. Newbold, E. Padilla-banks, R. Snyder, and W. Jefferson, Perinatal exposure to environmental estrogens and the development of obesity, Molecular Nutrition & Food Research, vol.49, issue.7, pp.912-919, 2007.
DOI : 10.1002/mnfr.200600259

J. Bispham, G. Gopalakrishnan, J. Dandrea, V. Wilson, H. Budge et al., Maternal Endocrine Adaptation throughout Pregnancy to Nutritional Manipulation: Consequences for Maternal Plasma Leptin and Cortisol and the Programming of Fetal Adipose Tissue Development, Endocrinology, vol.144, issue.8, pp.3575-85, 2003.
DOI : 10.1210/en.2003-0320

A. Riu, M. Grimaldi, A. Le-maire, G. Bey, K. Phillips et al., Peroxisome Proliferator-Activated Receptor ?? Is a Target for Halogenated Analogs of Bisphenol A, Environmental Health Perspectives, vol.119, issue.9, pp.1227-1259, 2011.
DOI : 10.1289/ehp.1003328

C. Hao, X. Cheng, H. Xia, and X. Ma, The endocrine disruptor mono-(2-ethylhexyl) phthalate promotes adipocyte differentiation and induces obesity in mice, Bioscience Reports, vol.278, issue.6, pp.619-2910, 2012.
DOI : 10.1074/jbc.M210062200

C. Hao, X. Cheng, H. Xia, and X. Ma, The Endocrine Disruptor 4-Nonylphenol Promotes Adipocyte Differentiation and Induces Obesity in Mice, Cellular Physiology and Biochemistry, vol.30, issue.2, pp.382-94, 2012.
DOI : 10.1159/000339032

C. Hao, X. Cheng, H. Xia, and X. Ma, The endocrine disruptor diethylstilbestrol induces adipocyte differentiation and promotes obesity in mice, Toxicology and Applied Pharmacology, vol.263, issue.1, 2012.
DOI : 10.1016/j.taap.2012.06.003

K. Flynn, S. Ferguson, K. Delclos, and R. Newbold, Effects of Genistein Exposure on Sexually Dimorphic Behaviors in Rats, Toxicological Sciences, vol.55, issue.2, pp.311-320, 2000.
DOI : 10.1093/toxsci/55.2.311

H. Park, J. Yang, S. Ambati, M. Della-fera, D. Hausman et al., Combined Effects of Genistein, Quercetin, and Resveratrol in Human and 3T3-L1 Adipocytes, Journal of Medicinal Food, vol.11, issue.4, pp.773-830077, 2008.
DOI : 10.1089/jmf.2008.0077

J. Molina-molina, A. Hillenweck, I. Jouanin, D. Zalko, J. Cravedi et al., Steroid receptor profiling of vinclozolin and its primary metabolites, Toxicology and Applied Pharmacology, vol.216, issue.1, pp.44-54, 2006.
DOI : 10.1016/j.taap.2006.04.005

K. Flynn, K. Delclos, R. Newbold, and S. Ferguson, Behavioral Responses of Rats Exposed to Long-Term Dietary Vinclozolin, Journal of Agricultural and Food Chemistry, vol.49, issue.3, pp.1658-65, 2001.
DOI : 10.1021/jf0008893

K. Kandulska, L. Nogowski, and T. Szkudelski, Effect of some phytoestrogens on metabolism of rat adipocytes, Reproduction Nutrition Development, vol.39, issue.4, pp.497-501, 1999.
DOI : 10.1051/rnd:19990408

URL : https://hal.archives-ouvertes.fr/hal-00900318

P. Phrakonkham, S. Viengchareun, C. Belloir, M. Lombes, Y. Artur et al., Dietary xenoestrogens differentially impair 3T3-L1 preadipocyte differentiation and persistently affect leptin synthesis, The Journal of Steroid Biochemistry and Molecular Biology, vol.110, issue.1-2, pp.95-103, 2008.
DOI : 10.1016/j.jsbmb.2008.02.006

T. Szkudelski, L. Nogowski, E. Pruszynska-oszmalek, P. Kaczmarek, and K. Szkudelska, Genistein restricts leptin secretion from rat adipocytes, The Journal of Steroid Biochemistry and Molecular Biology, vol.96, issue.3-4, 2005.
DOI : 10.1016/j.jsbmb.2005.04.033

K. Szkudelska, L. Nogowski, and T. Szkudelski, Genistein, a plant-derived isoflavone, counteracts the antilipolytic action of insulin in isolated rat adipocytes, The Journal of Steroid Biochemistry and Molecular Biology, vol.109, issue.1-2, 2008.
DOI : 10.1016/j.jsbmb.2007.12.006

W. Kouidhi, R. Berges, C. Tiffon, C. Desmetz, E. May et al., Perinatal xenohormone exposure impacts sweet preference and submandibular development in male rats, Oral Diseases, vol.8, issue.8, pp.812-835, 2013.
DOI : 10.1016/0031-9384(72)90135-7

I. Sahin, R. Serter, F. Karakurt, B. Demirbas, S. Guler et al., Leptin Levels Increase during Flutamide Therapy in Women with Polycystic Ovary Syndrome, Hormone Research in Paediatrics, vol.60, issue.5, pp.232-238, 2003.
DOI : 10.1159/000074037

W. Kouidhi, C. Desmetz, A. Nahdi, R. Berges, J. Cravedi et al., In Utero and Lactational Exposure to Low-Dose Genistein-Vinclozolin Mixture Affects the Development and Growth Factor mRNA Expression of the Submandibular Salivary Gland in Immature Female Rats, Toxicologic Pathology, vol.9, issue.4, pp.593-604, 2012.
DOI : 10.1074/jbc.270.34.19998

F. Eustache, F. Mondon, M. Canivenc-lavier, C. Lesaffre, Y. Fulla et al., Chronic Dietary Exposure to a Low-Dose Mixture of Genistein and Vinclozolin Modifies the Reproductive Axis, Testis Transcriptome, and Fertility, Environmental Health Perspectives, vol.117, issue.8, pp.1272-1281, 2009.
DOI : 10.1289/ehp.0800158.s1

E. Sheikh-saad, H. Meduri, G. Phrakonkham, P. Berges, R. Vacher et al., Abnormal peripubertal development of the rat mammary gland following exposure in utero and during lactation to a mixture of genistein and the food contaminant vinclozolin

E. Sheikh-saad, H. Toullec, A. Vacher, S. Pocard, M. Bieche et al., In utero and lactational exposure to vinclozolin and genistein induces genomic changes in the rat mammary gland, Journal of Endocrinology, vol.216, issue.2, pp.245-63, 2013.
DOI : 10.1530/JOE-12-0395

M. Vilela, E. Willingham, J. Buckley, B. Liu, K. Agras et al., Endocrine Disruptors and Hypospadias: Role of Genistein and the Fungicide Vinclozolin, Urology, vol.70, issue.3, pp.618-639, 2007.
DOI : 10.1016/j.urology.2007.05.004

C. Pelissero, B. Bennetau, P. Babin, L. Menn, F. Dunogues et al., The estrogenic activity of certain phytoestrogens in the siberian sturgeon Acipenser baeri, The Journal of Steroid Biochemistry and Molecular Biology, vol.38, issue.3, pp.293-302, 1991.
DOI : 10.1016/0960-0760(91)90100-J

J. Bursztyka, L. Debrauwer, E. Perdu, I. Jouanin, J. Jaeg et al., Biotransformation of vinclozolin in rat precision-cut liver slices: comparison with in vivo metabolic pattern, J Agric Food Chem Impact, vol.7, issue.2, pp.83-89, 20176.

P. Rat, C. Korwin-zmijowska, J. Warnet, and A. M. , Newin vitro fluorimetric microtitration assays for toxicological screening of drugs, Cell Biology and Toxicology, vol.282, issue.5-6, pp.329-366, 1994.
DOI : 10.1111/j.1768-322X.1986.tb00458.x

J. Kissane and E. Robins, The fluorometric measurement of deoxyribonucleic acid in animal tissues with special reference to the central nervous system, J Biol Chem, vol.233, pp.184-192, 1958.

S. Vankoningsloo, M. Piens, C. Lecocq, A. Gilson, D. Pauw et al., Mitochondrial dysfunction induces triglyceride accumulation in 3T3-L1 cells: role of fatty acid ??-oxidation and glucose, Journal of Lipid Research, vol.85, issue.6, pp.1133-1182, 2005.
DOI : 10.1152/ajpendo.00455.2001

A. Harmon and J. Harp, Differential effects of flavonoids on 3T3- L1 adipogenesis and lipolysis, Am J Physiol Cell Physiol, vol.280, pp.807-820, 2001.

S. Rayalam, M. Della-fera, J. Yang, H. Park, S. Ambati et al., Resveratrol potentiates genistein's antiadipogenic and proapoptotic effects in 3T3-L1 adipocytes, J Nutr, vol.137, pp.2668-73, 2007.

H. Park, M. Della-fera, D. Hausman, S. Rayalam, S. Ambati et al., Genistein inhibits differentiation of primary human adipocytes, The Journal of Nutritional Biochemistry, vol.20, issue.2, 2009.
DOI : 10.1016/j.jnutbio.2008.01.006

URL : http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1025.9938

K. Kristensen, S. Pedersen, and B. Richelsen, Regulation of Leptin by Steroid Hormones in Rat Adipose Tissue, Biochemical and Biophysical Research Communications, vol.259, issue.3, 1999.
DOI : 10.1006/bbrc.1999.0842

P. Leroy, S. Dessolin, P. Villageois, B. Moon, J. Friedman et al., Expression of ob Gene in Adipose Cells: REGULATION BY INSULIN, Journal of Biological Chemistry, vol.271, issue.5, pp.2365-2373, 1996.
DOI : 10.1074/jbc.271.5.2365