G. Lee and S. C. Gammie, GABAA receptor signaling in caudal periaqueductal gray regulates maternal aggression and maternal care in mice, Behav Brain Res, vol.213, pp.230-237, 2010.

M. Numan, D. S. Stolzenberg, A. A. Dellevigne, C. M. Correnti, and M. J. Numan, Temporary inactivation of ventral tegmental area neurons with either muscimol or baclofen reversibly disrupts maternal behavior in rats through different underlying mechanisms, Behav.Neurosci, vol.123, pp.740-51, 2009.

H. C. Salzberg, J. S. Lonstein, and J. M. Stern, GABA(A) receptor regulation of kyphotic nursing and female sexual behavior in the caudal ventrolateral periaqueductal gray of postpartum rats, Neuroscience, vol.114, pp.675-87, 2002.

Y. Yang, J. Qin, W. Chen, N. Sui, H. Chen et al., Behavioral and pharmacological investigation of anxiety and maternal responsiveness of postpartum female rats in a pup elevated plus maze, Behav Brain Res, vol.292, pp.414-441, 2015.

M. Febo, A. C. Felix-ortiz, and T. R. Johnson, Inactivation or inhibition of neuronal activity in the medial prefrontal cortex largely reduces pup retrieval and grouping in maternal rats, Brain Res, vol.1325, pp.77-88, 2010.

R. S. Bridges, D. K. Clifton, and C. H. Sawyer, Postpartum luteinizing hormone release and maternal behavior in the rat after late-gestational depletion of hypothalamic norepinephrine, Neuroendocrinology, vol.34, pp.286-91, 1982.

E. T. Cox, T. M. Jarrett, M. S. Mcmurray, K. Greenhill, V. E. Hofler et al., Combined norepinephrine/serotonergic reuptake inhibition: effects on maternal behavior, aggression, and oxytocin in the rat, Frontiers in psychiatry, vol.2, p.34, 2011.

C. Dickinson and E. B. Keverne, Importance of noradrenergic mechanisms in the olfactory bulbs for the maternal behaviour of mice, Physiol Behav, vol.43, pp.313-319, 1988.

F. Levy, R. Gervais, U. Kindermann, P. Orgeur, and V. Piketty, Importance of beta-noradrenergic receptors in the olfactory bulb of sheep for recognition of lambs, Behav.Neurosci, vol.104, pp.464-473, 1990.

M. A. Scotti, G. Lee, and S. C. Gammie, Maternal defense is modulated by beta adrenergic receptors in lateral septum in mice, Behav.Neurosci, vol.125, pp.434-479, 2011.

C. D. Smith, M. A. Holschbach, J. Olsewicz, and J. S. Lonstein, Effects of noradrenergic alpha-2 receptor antagonism or noradrenergic lesions in the ventral bed nucleus of the stria terminalis and medial preoptic area on maternal care in female rats, Psychopharmacology (Berl), vol.224, pp.263-76, 2012.

S. A. Thomas and R. D. Palmiter, Impaired maternal behavior in mice lacking norepinephrine and epinephrine, Cell, vol.91, pp.583-92, 1997.

B. L. Jacobs and E. C. Azmitia, Structure and function of the brain serotonin system, Physiol Rev, vol.72, pp.165-229, 1992.

F. G. Graeff, F. S. Guimaraes, T. G. De-andrade, and J. F. Deakin, Role of 5-HT in stress, anxiety, and depression, Pharmacol Biochem Behav, vol.54, pp.129-170, 1996.

R. Cools, A. C. Roberts, and T. W. Robbins, Serotoninergic regulation of emotional and behavioural control processes, Trends Cogn Sci, vol.12, pp.31-40, 2008.

I. Lucki, The spectrum of behaviors influenced by serotonin, Biol.Psychiatry, vol.44, pp.151-62, 1998.

K. P. Lesch, Linking emotion to the social brain. The role of the serotonin transporter in human social behaviour, EMBO reports, vol.8, pp.24-33, 2007.

M. Gemmel, E. Bogi, C. Ragan, M. Hazlett, M. Dubovicky et al., Perinatal selective serotonin reuptake inhibitor medication (SSRI) effects on social behaviors, neurodevelopment and the epigenome, Neurosci Biobehav Rev, vol.85, pp.102-116, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01619303

T. F. Oberlander, W. Warburton, S. Misri, J. Aghajanian, and C. Hertzman, Neonatal outcomes after prenatal exposure to selective serotonin reuptake inhibitor antidepressants and maternal depression using population-based linked health data, Arch Gen Psychiatry, vol.63, pp.898-906, 2006.

H. Zoega, H. Kieler, M. Norgaard, K. Furu, U. Valdimarsdottir et al., Use of SSRI and SNRI Antidepressants during Pregnancy: A Population-Based Study from Denmark, PLoS One, vol.10, p.144474, 2015.

R. A. Charlton, S. Jordan, A. Pierini, E. Garne, A. J. Neville et al., Selective serotonin reuptake inhibitor prescribing before, during and after pregnancy: a population-based study in six European regions, BJOG, vol.122, pp.1010-1030, 2015.

R. M. Hayes, P. Wu, R. C. Shelton, W. O. Cooper, W. D. Dupont et al., Maternal antidepressant use and adverse outcomes: a cohort study of 228,876 pregnancies, Am.J Obstet.Gynecol, vol.207, pp.1-9, 2012.

A. Lupattelli, O. Spigset, M. J. Twigg, K. Zagorodnikova, A. C. Mardby et al., Medication use in pregnancy: a cross-sectional, multinational web-based study, BMJ Open, vol.4, p.4365, 2014.

J. S. Lonstein, The dynamic serotonin system of the maternal brain, Arch Womens Ment Health, 2018.

A. Dahlstroem and K. Fuxe, Evidence for the Existence of Monoamine-Containing Neurons in the Central Nervous System. I. Demonstration of Monoamines in the Cell Bodies of Brain Stem Neurons, Acta Physiol Scand, vol.232, pp.1-55, 1964.

H. W. Steinbusch, Distribution of serotonin-immunoreactivity in the central nervous system of the rat-cell bodies and terminals, Neuroscience, vol.6, pp.557-618, 1981.

J. P. Hornung, The neuroanatomy fo the serotonergic system, Handbook of Behavioral Neuroscience, vol.21, pp.51-64, 2010.

C. A. Lowry, A. K. Evans, P. J. Gasser, M. W. Hale, D. R. Staub et al., Topographic organization and chemoarchitecture of the dorsal raphe nucleus and the median raphe nucleus, Serotonin and Sleep: Molecular, Functional and Clinical Aspects, pp.25-67, 2008.

D. J. Walther and M. Bader, A unique central tryptophan hydroxylase isoform, Biochem Pharmacol, vol.66, pp.1673-80, 2003.

L. F. Mohammad-zadeh, L. Moses, and S. M. Gwaltney-brant, Serotonin: a review. Journal of veterinary pharmacology and therapeutics, vol.31, pp.187-99, 2008.

L. Descarries, M. Riad, and M. Parent, Ultrastructure of the serotonin innervation fo the mammalian central nervous system, Handbook of Behavioral Neuroscience, pp.61-101, 2010.

J. Hannon and D. Hoyer, Molecular biology of 5-HT receptors, Behav Brain Res, vol.195, pp.198-213, 2008.

P. W. Burnet, S. L. Eastwood, K. Lacey, and P. J. Harrison, The distribution of 5-HT1A and 5-HT2A receptor mRNA in human brain, Brain Res, vol.676, pp.157-68, 1995.

D. T. Chalmers and S. J. Watson, Comparative anatomical distribution of 5-HT1A receptor mRNA and 5-HT1A binding in rat brain--a combined in situ hybridisation/in vitro receptor autoradiographic study, Brain Res, vol.561, pp.51-60, 1991.

M. Pompeiano, J. M. Palacios, and G. Mengod, Distribution and cellular localization of mRNA coding for 5-HT1A receptor in the rat brain: correlation with receptor binding, J Neurosci, vol.12, pp.440-53, 1992.

P. Stein, M. Savli, W. Wadsak, M. Mitterhauser, M. Fink et al., The serotonin-1A receptor distribution in healthy men and women measured by PET and [carbonyl-11C]WAY-100635, Eur J Nucl Med Mol Imaging, vol.35, pp.2159-68, 2008.

A. Pazos and J. M. Palacios, Quantitative autoradiographic mapping of serotonin receptors in the rat brain. I. Serotonin-1 receptors, Brain Res, vol.346, pp.205-235, 1985.

S. Hjorth and T. Magnusson, The 5-HT 1A receptor agonist, 8-OH-DPAT, preferentially activates cell body 5-HT autoreceptors in rat brain in vivo, Naunyn Schmiedebergs Arch Pharmacol, vol.338, pp.463-71, 1988.

G. Bonvento, B. Scatton, Y. Claustre, and L. Rouquier, Effect of local injection of 8-OH-DPAT into the dorsal or median raphe nuclei on extracellular levels of serotonin in serotonergic projection areas in the rat brain, Neurosci.Lett, vol.137, pp.101-105, 1992.

N. M. Barnes and T. Sharp, A review of central 5-HT receptors and their function, Neuropharmacology, vol.38, pp.1083-152, 1999.

K. P. Lesch and L. Gutknecht, Focus on The 5-HT1A receptor: emerging role of a gene regulatory variant in psychopathology and pharmacogenetics, Int J Neuropsychopharmacol, vol.7, pp.381-386, 2004.

V. Cornea-hebert, M. Riad, C. Wu, S. K. Singh, and L. Descarries, Cellular and subcellular distribution of the serotonin 5-HT2A receptor in the central nervous system of adult rat, J Comp Neurol, vol.409, pp.187-209, 1999.

A. Ettrup, C. Svarer, B. Mcmahon, S. Da-cunha-bang, S. Lehel et al., Serotonin 2A receptor agonist binding in the human brain with, vol.130, pp.167-174, 2016.

M. Pasqualetti, M. Ori, M. Castagna, D. Marazziti, G. B. Cassano et al., Distribution and cellular localization of the serotonin type 2C receptor messenger RNA in human brain, Neuroscience, vol.92, pp.601-612, 1999.

D. A. Clemett, T. Punhani, M. S. Duxon, T. P. Blackburn, and K. C. Fone, Immunohistochemical localisation of the 5-HT2C receptor protein in the rat CNS, Neuropharmacology, vol.39, pp.123-155, 2000.

M. Pompeiano, J. M. Palacios, and G. Mengod, Distribution of the serotonin 5-HT2 receptor family mRNAs: comparison between 5-HT2A and 5-HT2C receptors, Brain Res Mol Brain Res, vol.23, pp.163-78, 1994.

C. Gundlah, M. Pecins-thompson, W. E. Schutzer, and C. L. Bethea, Ovarian steroid effects on serotonin 1A, 2A and 2C receptor mRNA in macaque hypothalamus, Brain Res Mol Brain Res, vol.63, pp.325-364, 1999.

D. Hoyer, J. P. Hannon, and G. R. Martin, Molecular, pharmacological and functional diversity of 5-HT receptors, Pharmacol Biochem Behav, vol.71, pp.533-54, 2002.

H. Jovanovic, J. Lundberg, P. Karlsson, A. Cerin, T. Saijo et al., Sex differences in the serotonin 1A receptor and serotonin transporter binding in the human brain measured by PET, Neuroimage, vol.39, pp.1408-1427, 2008.

E. L. Moses-kolko, J. C. Price, N. Shah, S. Berga, S. M. Sereika et al., Age, sex, and reproductive hormone effects on brain serotonin-1A and serotonin-2A receptor binding in a healthy population, Neuropsychopharmacology, vol.36, pp.2729-2769, 2011.

D. W. Wooten, A. T. Hillmer, J. M. Moirano, D. L. Tudorascu, E. O. Ahlers et al., 5-HT1A sex based differences in Bmax, in vivo KD, and BPND in the nonhuman primate, Neuroimage, vol.77, pp.125-157, 2013.

L. Zhang, W. Ma, J. L. Barker, and D. R. Rubinow, Sex differences in expression of serotonin receptors (subtypes 1A and 2A) in rat brain: a possible role of testosterone, Neuroscience, vol.94, pp.251-260, 1999.

C. L. Bethea, N. Z. Lu, C. Gundlah, and J. M. Streicher, Diverse actions of ovarian steroids in the serotonin neural system, Front Neuroendocrinol, vol.23, pp.41-100, 2002.

F. J. Spielman, R. A. Mueller, and B. C. Corke, Cerebrospinal fluid concentration of 5-hydroxyindoleactic acid in pregnancy, Anesthesiology, vol.62, pp.193-198, 1985.

T. Sekiyama, Y. Nakatani, X. Yu, Y. Seki, I. Sato-suzuki et al., Increased blood serotonin concentrations are correlated with reduced tension/anxiety in healthy postpartum lactating women, Psychiatry Res, vol.209, pp.560-565, 2013.

M. Maes, R. Verkerk, S. Bonaccorso, W. Ombelet, E. Bosmans et al., Depressive and anxiety symptoms in the early puerperium are related to increased degradation of tryptophan into kynurenine, a phenomenon which is related to immune activation, Life Sci, vol.71, pp.1837-1885, 2002.

C. Veen, A. M. Myint, K. M. Burgerhout, M. J. Schwarz, G. Schutze et al., Tryptophan pathway alterations in the postpartum period and in acute postpartum psychosis and depression, J Affect.Disord, vol.189, pp.298-305, 2016.

A. A. Badawy, The tryptophan utilization concept in pregnancy, Obstet Gynecol Sci, vol.57, pp.249-59, 2014.

J. D. Fernstrom and R. J. Wurtman, Brain serotonin content: physiological regulation by plasma neutral amino acids, Science, vol.178, pp.414-420, 1972.

K. M. Harding and J. S. Lonstein, Extensive juvenile "babysitting" facilitates later adult maternal responsiveness, decreases anxiety, and increases dorsal raphe tryptophan hydroxylase-2 expression in female laboratory rats, Dev Psychobiol, vol.58, pp.492-508, 2016.

M. A. Holschbach and J. S. Lonstein, Motherhood and infant contact regulate neuroplasticity in the serotonergic midbrain dorsal raphe, Psychoneuroendocrinology, vol.76, pp.97-106, 2017.

R. Klink, M. Robichaud, and G. Debonnel, Gender and gonadal status modulation of dorsal raphe nucleus serotonergic neurons. Part I: effects of gender and pregnancy, Neuropharmacology, vol.43, pp.1119-1147, 2002.

N. J. Jury, B. A. Mccormick, N. D. Horseman, S. C. Benoit, and K. A. Gregerson, Enhanced responsiveness to selective serotonin reuptake inhibitors during lactation, PLoS One, vol.10, p.117339, 2015.

P. H. Desan, W. W. Woodmansee, S. M. Ryan, T. K. Smock, and S. F. Maier, Monoamine neurotransmitters and metabolites during the estrous cycle, pregnancy, and the postpartum period, Pharmacol.Biochem.Behav, vol.30, pp.563-571, 1988.

J. Glaser, V. A. Russell, A. S. De-villiers, J. A. Searson, and J. J. Taljaard, Rat brain monoamine and Serotonin S2 receptor changes during pregnancy, Neurochem Res, vol.15, pp.949-56, 1990.

A. H. Macbeth, C. Gautreaux, and V. N. Luine, Pregnant rats show enhanced spatial memory, decreased anxiety, and altered levels of monoaminergic neurotransmitters, Brain Res, vol.1241, pp.136-183, 2008.

J. S. Lonstein, M. Pereira, J. I. Morrell, C. A. Marler, and P. Behavior, Knobil and Neill's Physiology of Reproduction, pp.2371-2438, 2014.

M. Numan and D. S. Stolzenberg, Hypothalamic interaction with the mesolimbic dopamine system and the regulation of maternal responsiveness, Neurobiology of the parental brain, 2008.

J. S. Lonstein, J. M. Dominguez, S. K. Putnam, G. J. De-vries, and E. M. Hull, Intracellular preoptic and striatal monoamines in pregnant and lactating rats: possible role in maternal behavior, Brain Res, vol.970, pp.149-58, 2003.

C. D. Smith, C. C. Piasecki, M. Weera, J. Olszewicz, and J. S. Lonstein, Noradrenergic alpha-2 receptor modulators in the ventral bed nucleus of the stria terminalis: effects on anxiety behavior in postpartum and virgin female rats, Behav.Neurosci, vol.127, pp.582-97, 2013.

E. M. Vitale, C. L. Washington, and J. S. Lonstein, Female reproduction state influences raphe and forebrain serotonin 1A, 2A and 2C receptor expression, Society for Neuroscience, p.2017

J. Serrats, G. Mengod, and R. Cortes, Expression of serotonin 5-HT2C receptors in GABAergic cells of the anterior raphe nuclei, J Chem Neuroanat, vol.29, pp.83-91, 2005.

M. Pereira, Structural and Functional Plasticity in the Maternal Brain Circuitry, New Dir Child Adolesc Dev, pp.23-46, 2016.

J. L. Pawluski, K. G. Lambert, and C. H. Kinsley, Neuroplasticity in the maternal hippocampus: Relation to cognition and effects of repeated stress, Horm Behav, vol.77, pp.86-97, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01169791

B. Leuner and S. Sabihi, The birth of new neurons in the maternal brain: Hormonal regulation and functional implications, Front Neuroendocrinol, vol.41, pp.99-113, 2016.

B. Leuner, E. R. Glasper, and E. Gould, Parenting and plasticity, Trends Neurosci, vol.33, pp.465-73, 2010.

F. Levy, G. Gheusi, and M. Keller, Plasticity of the parental brain: a case for neurogenesis, J Neuroendocrinol, vol.23, pp.984-93, 2011.
URL : https://hal.archives-ouvertes.fr/hal-01129516

J. L. Pawluski, D. L. Van-den-hove, I. Rayen, J. Prickaerts, and H. W. Steinbusch, Stress and the pregnant female: Impact on hippocampal cell proliferation, but not affective-like behaviors, Horm Behav, vol.59, pp.572-80, 2011.

J. L. Pawluski, V. E. Barakauskas, and L. A. Galea, Pregnancy decreases oestrogen receptor alpha expression and pyknosis, but not cell proliferation or survival, in the hippocampus, J Neuroendocrinol, vol.22, pp.248-57, 2010.

F. Levy, M. Batailler, M. Meurisse, and M. Migaud, Adult Neurogenesis in Sheep: Characterization and Contribution to Reproduction and Behavior, Frontiers in neuroscience, vol.11, p.570, 2017.

J. L. Pawluski and L. A. Galea, Reproductive experience alters hippocampal neurogenesis during the postpartum period in the dam, Neuroscience, vol.149, pp.53-67, 2007.

R. Corona, M. Meurisse, F. Cornilleau, C. Moussu, M. Keller et al., Disruption of adult olfactory neurogenesis induces deficits in maternal behavior in sheep, Behav Brain Res, vol.347, pp.124-131, 2018.

M. Furuta and R. S. Bridges, Gestation-induced cell proliferation in the rat brain, Brain Res Dev Brain Res, vol.156, pp.61-67, 2005.

C. M. Larsen and D. R. Grattan, Prolactin-induced mitogenesis in the subventricular zone of the maternal brain during early pregnancy is essential for normal postpartum behavioral responses in the mother, Endocrinology, vol.151, pp.3805-3819, 2010.

T. Shingo, C. Gregg, E. Enwere, H. Fujikawa, R. Hassam et al., Pregnancy-stimulated neurogenesis in the adult female forebrain mediated by prolactin, Science, vol.299, pp.117-137, 2003.

G. L. Ming and H. Song, Adult neurogenesis in the mammalian central nervous system, Annu Rev Neurosci, vol.28, pp.223-50, 2005.

E. Arenas, M. Denham, and J. C. Villaescusa, How to make a midbrain dopaminergic neuron, Development, vol.142, pp.1918-1954, 2015.

G. Chechik, I. Meilijson, and E. Ruppin, Neuronal regulation: A mechanism for synaptic pruning during brain maturation, Neural Comput, vol.11, pp.2061-80, 1999.

M. Fricker, A. M. Tolkovsky, V. Borutaite, M. Coleman, and G. C. Brown, Neuronal Cell Death. Physiol Rev, vol.98, pp.813-880, 2018.

J. L. Pawluski, S. Brummelte, C. K. Barha, T. M. Crozier, and L. A. Galea, Effects of steroid hormones on neurogenesis in the hippocampus of the adult female rodent during the estrous cycle, pregnancy, lactation and aging, Front Neuroendocrinol, vol.30, pp.343-57, 2009.

B. Leuner, C. Mirescu, L. Noiman, and E. Gould, Maternal experience inhibits the production of immature neurons in the hippocampus during the postpartum period through elevations in adrenal steroids, Hippocampus, vol.17, pp.434-476, 2007.

M. Darnaudery, M. Perez-martin, F. Favero, C. Gomez-roldan, L. M. Garcia-segura et al., Early motherhood in rats is associated with a modification of hippocampal function, Psychoneuroendocrinology, vol.32, pp.803-815, 2007.

A. L. Barofsky, J. Taylor, and M. Vj, Dorsal raphe-hypothalamic projections provide the stimulatory serotonergic input to suckling-induced prolactin release, Endocrinology, vol.113, pp.1894-903, 1983.

A. L. Barofsky, J. Taylor, Y. Tizabi, R. Kumar, and K. Jones-quartey, Specific neurotoxin lesions of median raphe serotonergic neurons disrupt maternal behavior in the lactating rat, Endocrinology, vol.113, pp.1884-93, 1983.

M. A. Holschbach, E. M. Vitale, and J. S. Lonstein, Serotonin-specific lesions of the dorsal raphe disrupt maternal aggression and caregiving in postpartum rats, Behav Brain Res, vol.348, pp.53-64, 2018.

R. H. Melloni, J. , and L. A. Ricci, Adolescent exposure to anabolic/androgenic steroids and the neurobiology of offensive aggression: a hypothalamic neural model based on findings in pubertal Syrian hamsters, Horm Behav, vol.58, pp.177-91, 2010.

J. I. Terranova, C. F. Ferris, and H. E. Albers, Sex Differences in the Regulation of Offensive Aggression and Dominance by Arginine-Vasopressin, Frontiers in endocrinology, vol.8, p.308, 2017.

T. Hendricks, N. Francis, D. Fyodorov, and E. S. Deneris, The ETS domain factor Pet-1 is an early and precise marker of central serotonin neurons and interacts with a conserved element in serotonergic genes, J Neurosci, vol.19, pp.10348-56, 1999.

J. K. Lerch-haner, D. Frierson, L. K. Crawford, S. G. Beck, and E. S. Deneris, Serotonergic transcriptional programming determines maternal behavior and offspring survival, Nat.Neurosci, 2008.

N. Alenina, D. Kikic, M. Todiras, V. Mosienko, F. Qadri et al., Growth retardation and altered autonomic control in mice lacking brain serotonin, Proc Natl Acad Sci U S A, vol.106, pp.10332-10339, 2009.

S. Girirajan and S. H. Elsea, Abnormal maternal behavior, altered sociability, and impaired serotonin metabolism in Rai1-transgenic mice, Mammalian genome : official journal of the International Mammalian Genome Society, vol.20, pp.247-55, 2009.

M. Angoa-perez, M. J. Kane, C. E. Sykes, S. A. Perrine, M. W. Church et al., Brain serotonin determines maternal behavior and offspring survival, Genes Brain Behav, vol.13, pp.579-91, 2014.

D. Maestripieri, C. L. Hoffman, G. M. Anderson, C. S. Carter, and J. D. Higley, Mother-infant interactions in free-ranging rhesus macaques: relationships between physiological and behavioral variables, vol.96, pp.613-622, 2009.

D. Maestripieri, S. G. Lindell, and J. D. Higley, Intergenerational transmission of maternal behavior in rhesus macaques and its underlying mechanisms, Dev Psychobiol, vol.49, pp.165-71, 2007.

M. J. Bakermans-kranenburg and M. H. Van-ijzendoorn, Oxytocin receptor (OXTR) and serotonin transporter (5-HTT) genes associated with observed parenting, Soc Cogn Affect Neurosci, vol.3, pp.128-162, 2008.

V. Mileva-seitz, J. Kennedy, L. Atkinson, M. Steiner, R. Levitan et al., Serotonin transporter allelic variation in mothers predicts maternal sensitivity, behavior and attitudes toward 6-month-old infants, Genes Brain Behav, vol.10, pp.325-358, 2011.

R. A. Cents, R. Kok, H. Tiemeier, N. Lucassen, E. Szekely et al., Lambregtse-van den Berg, Variations in maternal 5-HTTLPR affect observed sensitive parenting, J Child Psychol Psychiatry, vol.55, pp.1025-1057, 2014.

M. L. Sturge-apple, D. Cicchetti, P. T. Davies, and J. H. Suor, Differential susceptibility in spillover between interparental conflict and maternal parenting practices: evidence for OXTR and 5-HTT genes, J Fam Psychol, vol.26, pp.431-473, 2012.

J. Belsky, C. Jonassaint, M. Pluess, M. Stanton, B. Brummett et al., Vulnerability genes or plasticity genes?, Mol.Psychiatry, vol.14, pp.746-54, 2009.

C. Yoshihara, M. Numan, and K. O. Kuroda, Oxytocin and Parental Behaviors, Current topics in behavioral neurosciences, vol.35, pp.119-153, 2018.

T. M. Cunha, S. J. King, A. S. Fleming, and F. Levy, Oxytocin receptors in the nucleus accumbens shell are involved in the consolidation of maternal memory in postpartum rats, Horm Behav, vol.59, pp.14-21, 2011.
URL : https://hal.archives-ouvertes.fr/hal-01129514

D. E. Olazabal and L. J. Young, Oxytocin receptors in the nucleus accumbens facilitate "spontaneous" maternal behavior in adult female prairie voles, Neuroscience, vol.141, pp.559-68, 2006.

C. A. Pedersen, J. D. Caldwell, C. Walker, G. Ayers, and G. A. Mason, Oxytocin activates the postpartum onset of rat maternal behavior in the ventral tegmental and medial preoptic areas, Behav.Neurosci, vol.108, pp.1163-71, 1994.

D. K. Shahrokh, T. Y. Zhang, J. Diorio, A. Gratton, and M. J. Meaney, Oxytocin-dopamine interactions mediate variations in maternal behavior in the rat, Endocrinology, vol.151, pp.2276-86, 2010.

Z. A. Grieb and J. S. Lonstein, Effects of reproductive state on the expression of oxytocin receptor mRNA and protein in the midbrain raphe nuclei of female rats, Society for Neuroscience, 2015.

R. Yoshimura, H. Kiyama, T. Kimura, T. Araki, H. Maeno et al., Localization of oxytocin receptor messenger ribonucleic acid in the rat brain, Endocrinology, vol.133, pp.1239-1285, 1993.

F. Hernandez-vazquez, J. Garduno, and S. Hernandez-lopez, GABAergic modulation of serotonergic neurons in the dorsal raphe nucleus. Reviews in the Neurosciences In press, 2018.

J. H. Pagani, S. K. Williams-avram, Z. Cui, J. Song, E. Mezey et al., Raphe serotonin neuron-specific oxytocin receptor knockout reduces aggression without affecting anxiety-like behavior in male mice only, Genes Brain Behav, vol.14, pp.167-76, 2015.

R. L. Carhart-harris and D. J. Nutt, Serotonin and brain function: a tale of two receptors, J Psychopharmacol, vol.31, pp.1091-1120, 2017.

C. Bendotti and R. Samanin, 8-Hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) elicits eating in free-feeding rats by acting on central serotonin neurons, Eur J Pharmacol, vol.121, pp.147-50, 1986.
DOI : 10.1016/0014-2999(86)90405-x

W. J. Mcbride, J. M. Murphy, G. J. Gatto, A. D. Levy, L. Lumeng et al., Serotonin and dopamine systems regulating alcohol intake, Alcohol Alcohol Suppl, vol.1, pp.411-417, 1991.

H. J. Cassaday, E. L. Simpson, and E. A. Gaffan, Rapid visual learning in the rat: effects at the 5-HT1a receptor subtype, Q J Exp Psychol B, vol.53, pp.225-263, 2000.

K. A. Clissold, E. Choi, and W. E. Pratt, Serotonin 1A, 1B, and 7 receptors of the rat medial nucleus accumbens differentially regulate feeding, water intake, and locomotor activity, vol.112, pp.96-103, 2013.

C. L. Burton, Z. Rizos, M. Diwan, J. N. Nobrega, and P. J. Fletcher, Antagonizing 5-HT(2)A receptors with M100907 and stimulating 5-HT(2)C receptors with Ro60-0175 blocks cocaineinduced locomotion and zif268 mRNA expression in Sprague-Dawley rats, Behav Brain Res, vol.240, pp.171-81, 2013.

P. R. Albert, F. Vahid-ansari, and C. Luckhart, Serotonin-prefrontal cortical circuitry in anxiety and depression phenotypes: pivotal role of pre-and post-synaptic 5-HT1A receptor expression, Front Behav Neurosci, vol.8, p.199, 2014.

E. M. Snoeren, J. G. Veening, B. Olivier, and R. S. Oosting, Serotonin 1A receptors and sexual behavior in female rats: a review, Pharmacol Biochem Behav, vol.121, pp.43-52, 2014.

A. Ferreira, O. Picazo, N. Uriarte, M. Pereira, and A. Fernandez-guasti, Inhibitory effect of buspirone and diazepam, but not of 8-OH-DPAT, on maternal behavior and aggression, Pharmacol Biochem Be, vol.66, pp.389-396, 2000.

H. Yoshimura and N. Ogawa, Ethopharmacology of maternal aggression in mice: effects of diazepam and SM-3997, Eur J Pharmacol, vol.200, pp.147-53, 1991.

R. M. De-almeida and A. B. Lucion, Effects of intracerebroventricular administration of 5-HT receptor agonists on the maternal aggression of rats, Eur J Pharmacol, vol.264, pp.445-453, 1994.

C. P. Veiga, K. A. Miczek, A. B. Lucion, and R. M. Almeida, Effect of 5-HT1B receptor agonists injected into the prefrontal cortex on maternal aggression in rats, Braz J Med Biol Res, vol.40, pp.825-855, 2007.

B. Olivier, J. Mos, R. Van-oorschot, and R. Hen, Serotonin receptors and animal models of aggressive behavior, Pharmacopsychiatry, vol.28, issue.2, pp.80-90, 1995.

R. M. De-almeida and A. B. , Lucion, 8-OH-DPAT in the median raphe, dorsal periaqueductal gray and corticomedial amygdala nucleus decreases, but in the medial septal area it can increase maternal aggressive behavior in rats, Psychopharmacology (Berl), vol.134, pp.392-400, 1997.

C. P. Da-veiga, K. A. Miczek, A. B. Lucion, and R. M. De-almeida, Social instigation and aggression in postpartum female rats: role of 5-Ht1A and 5-Ht1B receptors in the dorsal raphe nucleus and prefrontal cortex, vol.213, pp.475-87, 2011.

X. Li, X. Ding, R. Wu, L. Chen, J. Gao et al., A behavioral mechanistic investigation of the role of 5-HT1A receptors in the mediation of rat maternal behavior, Pharmacol Biochem Behav, vol.169, pp.16-26, 2018.

C. Zhao and M. Li, Sedation and disruption of maternal motivation underlie the disruptive effects of antipsychotic treatment on rat maternal behavior, Pharmacol Biochem Behav, vol.92, pp.147-56, 2009.

R. Wu, C. Davis, and M. Li, Behavioral mechanisms underlying the maternal disruptive effect of serotonin 5-HT2A receptor activation in Sprague-Dawley rats, J Neural Transm, 2018.

R. Wu, J. Gao, S. Chou, C. Davis, and M. Li, Behavioral, pharmacological and neuroanatomical analysis of serotonin 2C receptor agonism on maternal behavior in rats, Psychoneuroendocrinology, vol.73, pp.252-262, 2016.

L. Svensson and S. Ahlenius, Enhancement by the putative 5-HT receptor agonist 8-OH-2-(di-npropylamino)tetralin of the acoustic startle response in the rat, Psychopharmacology (Berl), pp.104-111, 1983.

K. P. Nanry and H. A. Tilson, The role of 5HT1A receptors in the modulation of the acoustic startle reflex in rats, Psychopharmacology (Berl), pp.507-520, 1989.

L. H. Conti, Interactions between corticotropin-releasing factor and the serotonin 1A receptor system on acoustic startle amplitude and prepulse inhibition of the startle response in two rat strains, Neuropharmacology, vol.62, pp.256-63, 2012.

M. Li, P. Davidson, R. Budin, S. Kapur, and A. S. Fleming, Effects of typical and atypical antipsychotic drugs on maternal behavior in postpartum female rats, Schizophr Res, vol.70, pp.69-80, 2004.

M. Li, R. Budin, A. S. Fleming, and S. Kapur, Effects of chronic typical and atypical antipsychotic drug treatment on maternal behavior in rats, Schizophr Res, vol.75, pp.325-361, 2005.

C. Zhao and M. Li, c-Fos identification of neuroanatomical sites associated with haloperidol and clozapine disruption of maternal behavior in the rat, Neuroscience, vol.166, pp.1043-55, 2010.

J. Gao, R. Wu, C. Davis, and M. Li, Activation of 5-HT2A receptor disrupts rat maternal behavior, Neuropharmacology, vol.128, pp.96-105, 2018.

W. Chen, Q. Zhang, W. Su, H. Zhang, Y. Yang et al., Effects of 5-hydroxytryptamine 2C receptor agonist MK212 and 2A receptor antagonist MDL100907 on maternal behavior in postpartum female rats, Pharmacol.Biochem.Behav, vol.117, pp.25-33, 2014.

J. Kohl, A. E. Autry, and C. Dulac, The neurobiology of parenting: A neural circuit perspective, Bioessays, vol.39, pp.1-11, 2017.

J. Barrett and A. S. Fleming, Annual Research Review: All mothers are not created equal: neural and psychobiological perspectives on mothering and the importance of individual differences, J Child Psychol Psychiatry, vol.52, pp.368-97, 2011.

J. S. Lonstein and A. S. Fleming, Parental behaviors in rats and mice, Curr Protoc Neurosci Chapter, vol.8, p.15, 2002.

S. Hansen, Maternal behavior of female rats with 6-OHDA lesions in the ventral striatum: characterization of the pup retrieval deficit, Physiol Behav, vol.55, pp.615-635, 1994.

J. T. Curtis and Z. Wang, Ventral tegmental area involvement in pair bonding in male prairie voles, Physiol Behav, vol.86, pp.338-384, 2005.

T. H. Ahern, M. E. Modi, J. P. Burkett, and L. J. Young, Evaluation of two automated metrics for analyzing partner preference tests, J Neurosci Methods, vol.182, pp.180-188, 2009.

D. Agrati, A. Fernandez-guasti, and A. Ferreira, The reproductive stage and experience of sexually receptive mothers alter their preference for pups or males, Behav Neurosci, vol.122, pp.998-1004, 2008.

D. Agrati, M. Ferreno, G. Marin, N. Uriarte, M. J. Zuluaga et al., Previous and recent maternal experiences modulate pups' incentive value relative to a male without affecting maternal behavior in postpartum estrous rats, J Physiol Paris, 2016.

B. Moghaddam and H. Homayoun, Divergent plasticity of prefrontal cortex networks, Neuropsychopharmacology, vol.33, pp.42-55, 2008.

M. V. Puig and A. T. Gulledge, Serotonin and prefrontal cortex function: neurons, networks, and circuits, Molecular neurobiology, vol.44, pp.449-64, 2011.

M. V. Puig, A. T. Gulledge, E. K. Lambe, and G. Gonzalez-burgos, Editorial: Neuromodulation of executive circuits, Front Neural Circuits, vol.9, p.58, 2015.

N. C. Anastasio, S. J. Stutz, L. H. Fink, S. E. Swinford-jackson, R. M. Sears et al., Serotonin (5-HT) 5-HT2A Receptor (5-HT2AR):5-HT2CR Imbalance in Medial Prefrontal Cortex Associates with Motor Impulsivity, vol.6, pp.1248-58, 2015.

P. Vazquez-borsetti, R. Cortes, and F. Artigas, Pyramidal neurons in rat prefrontal cortex projecting to ventral tegmental area and dorsal raphe nucleus express 5-HT2A receptors, Cereb Cortex, vol.19, pp.1678-86, 2009.

P. Celada, M. V. Puig, J. M. Casanovas, G. Guillazo, and F. Artigas, Control of dorsal raphe serotonergic neurons by the medial prefrontal cortex: Involvement of serotonin-1A, GABA(A), and glutamate receptors, J Neurosci, vol.21, pp.9917-9946, 2001.

P. Celada, M. V. Puig, R. Martin-ruiz, J. M. Casanovas, and F. Artigas, Control of the serotonergic system by the medial prefrontal cortex: potential role in the etiology of PTSD and depressive disorders, Neurotox Res, vol.4, pp.409-419, 2002.

J. Gao, R. Wu, C. Davis, and M. Li, Activation of 5-HT2A receptor disrupts rat maternal behavior, Neuropharmacology, 2017.

M. Morales and E. B. Margolis, Ventral tegmental area: cellular heterogeneity, connectivity and behaviour, Nat Rev Neurosci, vol.18, pp.73-85, 2017.

J. L. Pawluski, J. S. Lonstein, and A. S. Fleming, The Neurobiology of Postpartum Anxiety and Depression, Trends Neurosci, vol.40, pp.106-120, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01452985

P. Almond, Postnatal depression: a global public health perspective, Perspect Public Health, vol.129, pp.221-228, 2009.

B. M. Leung and B. J. Kaplan, Perinatal depression: prevalence, risks, and the nutrition link--a review of the literature, J Am Diet Assoc, vol.109, pp.1566-75, 2009.

S. M. Marcus, Depression during pregnancy: rates, risks and consequences--Motherisk Update, Can J Clin Pharmacol, vol.16, pp.15-22, 2008.

K. M. Hillerer, I. D. Neumann, and D. A. Slattery, From stress to postpartum mood and anxiety disorders: how chronic peripartum stress can impair maternal adaptations, Neuroendocrinology, vol.95, pp.22-38, 2012.

N. M. Talge, C. Neal, and V. Glover, Antenatal maternal stress and long-term effects on child neurodevelopment: how and why?, J Child Psychol Psychiatry, vol.48, pp.245-61, 2007.

T. Field, Handbook of Parenting, L. Erlbaum Associates, new Jersey, 1995.

T. Field, B. Healy, M. Goldstein, and M. Guthertz, Behavior-state matching and synchrony in mother-infant interactions of nondepressed versus depressed dyads, Dev. Psychobiol, vol.26, pp.7-14, 1990.

A. S. Fleming, D. N. Ruble, G. L. Flett, and D. Shaul, Postpartum Adjustment in First-Time Mothers: Relations between Mood, Maternal Attitudes and Mother-Infant Interactions, Dev. Psychobiol, vol.24, pp.71-81, 1988.

F. A. Champagne and M. J. Meaney, Stress during gestation alters postpartum maternal care and the development of the offspring in a rodent model, Biol.Psychiatry, vol.59, pp.1227-1262, 2006.

B. Leuner, P. J. Fredericks, C. Nealer, and C. Albin-brooks, Chronic gestational stress leads to depressive-like behavior and compromises medial prefrontal cortex structure and function during the postpartum period, PLoS One, vol.9, p.89912, 2014.

J. W. Smith, J. R. Seckl, A. T. Evans, B. Costall, and J. W. Smythe, Gestational stress induces postpartum depression-like behaviour and alters maternal care in rats, Psychoneuroendocrinology, vol.29, pp.227-271, 2004.

S. M. O'mahony, A. M. Myint, D. Van-den-hove, L. Desbonnet, H. Steinbusch et al., Gestational stress leads to depressive-like behavioural and immunological changes in the rat, Neuroimmunomodulation, vol.13, pp.82-90, 2006.

P. Blier and M. E. Mansari, Serotonin and beyond: therapeutics for major depression, Philosophical transactions of the Royal Society of London. Series B, Biological sciences, p.368, 2012.

M. Hamon and P. Blier, Monoamine neurocircuitry in depression and strategies for new treatments, Prog Neuropsychopharmacol Biol Psychiatry, vol.45, pp.54-63, 2013.

E. Maurer-spurej, C. Pittendreigh, and S. Misri, Platelet serotonin levels support depression scores for women with postpartum depression, J Psychiatry Neurosci, vol.32, pp.23-32, 2007.

J. Sanjuan, R. Martin-santos, L. Garcia-esteve, J. M. Carot, R. Guillamat et al., Mood changes after delivery: role of the serotonin transporter gene, Br J Psychiatry, vol.193, pp.383-391, 2008.

E. B. Binder, D. J. Newport, E. B. Zach, A. K. Smith, T. C. Deveau et al., A serotonin transporter gene polymorphism predicts peripartum depressive symptoms in an at-risk psychiatric cohort, J Psychiatr Res, vol.44, pp.640-646, 2010.

C. Mitchell, D. Notterman, J. Brooks-gunn, J. Hobcraft, I. Garfinkel et al., Role of mother's genes and environment in postpartum depression, Proc Natl Acad Sci U S A, vol.108, pp.8189-93, 2011.

E. L. Moses-kolko, K. L. Wisner, J. C. Price, S. L. Berga, W. C. Drevets et al., Serotonin 1A receptor reductions in postpartum depression: a positron emission tomography study, vol.89, pp.685-92, 2008.

M. Gemmel, I. Rayen, E. Van-donkelaar, T. Loftus, H. W. Steinbusch et al., Gestational stress and fluoxetine treatment differentially affect plasticity, methylation and serotonin levels in the PFC and hippocampus of rat dams, Neuroscience, vol.327, pp.32-43, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01301509

A. Stamatakis, T. Kalpachidou, A. Raftogianni, E. Zografou, A. Tzanou et al., Rat dams exposed repeatedly to a daily brief separation from the pups exhibit increased maternal behavior, decreased anxiety and altered levels of receptors for estrogens (ERalpha, ERbeta), oxytocin and serotonin (5-HT1A) in their brain, Psychoneuroendocrinology, vol.52, pp.212-240, 2015.

B. Szewczyk, K. Kotarska, M. Daigle, P. Misztak, M. Sowa-kucma et al., Stress-induced alterations in 5-HT1A receptor transcriptional modulators NUDR and Freud-1, Int J Neuropsychopharmacol, vol.17, pp.1763-75, 2014.

M. C. Kimmel, E. Cox, C. Schiller, E. Gettes, and S. Meltzer-brody, Pharmacologic Treatment of Perinatal Depression, Obstet Gynecol Clin North Am, vol.45, pp.419-440, 2018.

W. O. Cooper, M. E. Willy, S. J. Pont, and W. A. Ray, Increasing use of antidepressants in pregnancy, Am.J Obstet.Gynecol, vol.196, pp.1-5, 2007.

J. H. Kristensen, K. F. Ilett, L. P. Hackett, P. Yapp, M. Paech et al., Distribution and excretion of fluoxetine and norfluoxetine in human milk, Br J Clin Pharmacol, vol.48, pp.521-528, 1999.

T. F. Oberlander, J. A. Gingrich, and M. S. Ansorge, Sustained neurobehavioral effects of exposure to SSRI antidepressants during development: molecular to clinical evidence, Clin Pharmacol Ther, vol.86, pp.672-679, 2009.

S. M. Hutchison, L. C. Masse, J. L. Pawluski, and T. F. Oberlander, Perinatal selective serotonin reuptake inhibitor (SSRI) effects on body weight at birth and beyond: A review of animal and human studies, Reprod Toxicol, vol.77, pp.109-121, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01740002

J. D. Olivier, H. Akerud, H. Kaihola, J. L. Pawluski, A. Skalkidou et al., The effects of maternal depression and maternal selective serotonin reuptake inhibitor exposure on offspring, Frontiers in cellular neuroscience, vol.7, p.73, 2013.

J. R. Homberg, D. Schubert, and P. Gaspar, New perspectives on the neurodevelopmental effects of SSRIs, Trends Pharmacol Sci, vol.31, pp.60-65, 2010.

Y. Huang, H. Xu, H. Li, H. Yang, Y. Chen et al., Pre-gestational stress reduces the ratio of 5-HIAA to 5-HT and the expression of 5-HT1A receptor and serotonin transporter in the brain of foetal rat, BMC Neurosci, vol.13, p.22, 2012.

M. Gemmel, M. Hazlett, E. Bogi, S. De-lacalle, L. A. Hill et al., Perinatal fluoxetine effects on social play, the HPA system, and hippocampal plasticity in pre-adolescent male and female rats: Interactions with pre-gestational maternal stress, Psychoneuroendocrinology, vol.84, pp.159-171, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01579611

D. N. Kyriacou and R. J. Lewis, Confounding by Indication in Clinical Research, JAMA, vol.316, pp.1818-1819, 2016.

T. F. Oberlander and L. Zwaigenbaum, Disentangling Maternal Depression and Antidepressant Use During Pregnancy as Risks for Autism in Children, JAMA, vol.317, pp.1533-1534, 2017.

S. Brummelte, E. Mc-glanaghy, A. Bonnin, and T. F. Oberlander, Developmental changes in serotonin signaling: Implications for early brain function, behavior and adaptation, Neuroscience, vol.342, pp.212-231, 2017.

J. L. Pawluski and M. Gemmel, Perinatal SSRI medications and offspring hippocampal plasticity: interaction with maternal stress and sex, Hormones (Athens), vol.17, pp.15-24, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01863048

P. N. Reebye, S. J. Morison, H. Panikkar, S. Misri, and R. E. Grunau, Affect expression in prenatally psychotropic exposed and nonexposedmother-infant dyads, Infant Mental Health Journal, vol.23, pp.403-416, 2002.

W. M. Weikum, L. C. Mayes, R. E. Grunau, U. Brain, and T. F. Oberlander, The impact of prenatal serotonin reuptake inhibitor (SRI) antidepressant exposure and maternal mood on mother-infant interactions at 3 months of age, Infant Behav Dev, vol.36, pp.485-93, 2013.

J. M. Johns, P. W. Joyner, M. S. Mcmurray, D. L. Elliott, V. E. Hofler et al., The effects of dopaminergic/serotonergic reuptake inhibition on maternal behavior, maternal aggression, and oxytocin in the rat, Pharmacol.Biochem.Behav, vol.81, pp.769-85, 2005.

J. M. Kott, S. M. Mooney-leber, J. Li, and S. Brummelte, Elevated stress hormone levels and antidepressant treatment starting before pregnancy affect maternal care and litter characteristics in an animal model of depression, Behav Brain Res, vol.348, pp.101-114, 2018.

J. L. Workman, A. R. Gobinath, N. F. Kitay, C. Chow, S. Brummelte et al., Parity modifies the effects of fluoxetine and corticosterone on behavior, stress reactivity, and hippocampal neurogenesis, Neuropharmacology, vol.105, pp.443-453, 2016.

J. L. Pawluski, T. D. Charlier, M. Fillet, V. Houbart, H. T. Crispin et al., Chronic fluoxetine treatment and maternal adversity differentially alter neurobehavioral outcomes in the rat dam, Behav Brain Res, vol.228, pp.159-68, 2012.

J. Pawluski, T. Charlier, M. Fillet, V. Houbart, H. Crispin et al., Chronic fluoxetine treatment and maternal adversity differentially alter neurobehavioral outcomes in the rat dam, Behav Brain Res, vol.228, pp.159-68, 2012.

S. Mitra, M. Mucha, S. Owen, and A. Bult-ito, Postpartum Lactation-Mediated Behavioral Outcomes and Drug Responses in a Spontaneous Mouse Model of Obsessive-Compulsive Disorder, ACS Chem Neurosci, vol.8, pp.2683-2697, 2017.

M. Gemmel, D. Harmeyer, E. Bogi, M. Fillet, L. A. Hill et al., Perinatal fluoxetine increases hippocampal neurogenesis and reverses the lasting effects of pre-gestational stress on serum corticosterone, but not on maternal behavior, in the rat dam, Behav Brain Res, vol.339, pp.222-231, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01699220

V. Kiryanova, S. J. Meunier, H. A. Vecchiarelli, M. N. Hill, and R. H. Dyck, Effects of maternal stress and perinatal fluoxetine exposure on behavioral outcomes of adult male offspring, Neuroscience, vol.320, pp.281-96, 2016.

A. R. Gobinath, R. J. Richardson, C. Chow, J. L. Workman, S. E. Lieblich et al., Voluntary running influences the efficacy of fluoxetine in a model of postpartum depression, Neuropharmacology, vol.128, pp.106-118, 2018.

K. Belovicova, E. Bogi, R. Koprdova, E. Ujhazy, M. Mach et al., Effects of venlafaxine and chronic unpredictable stress on behavior and hippocampal neurogenesis of rat dams, Neuro Endocrinol Lett, vol.38, pp.19-26, 2017.

N. Svirsky, S. Levy, and R. Avitsur, Prenatal exposure to selective serotonin reuptake inhibitors (SSRI) increases aggression and modulates maternal behavior in offspring mice, Dev Psychobiol, vol.58, pp.71-82, 2016.

J. L. Pawluski, U. Brain, G. L. Hammond, and T. F. Oberlander, Selective serotonin reuptake inhibitor effects on neural biomarkers of perinatal depression, Arch Womens Ment Health, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01976469

J. D. Bremner, M. Narayan, E. R. Anderson, L. H. Staib, H. L. Miller et al., Hippocampal volume reduction in major depression, Am J Psychiatry, vol.157, pp.115-123, 2000.

R. L. Djavadian, Serotonin and neurogenesis in the hippocampal dentate gyrus of adult mammals, Acta Neurobiol Exp (Wars), vol.64, pp.189-200, 2004.

A. Dranovsky and R. Hen, Hippocampal neurogenesis: regulation by stress and antidepressants, Biol.Psychiatry, vol.59, pp.1136-1179, 2006.

J. Medina and J. L. Workman, Maternal experience and adult neurogenesis in mammals: Implications for maternal care, cognition, and mental health, J Neurosci Res, 2018.

L. A. Galea, B. Leuner, and D. A. Slattery, Hippocampal plasticity during the peripartum period: influence of sex steroids, stress and ageing, J Neuroendocrinol, vol.26, pp.641-649, 2014.

A. Haim, C. Albin-brooks, M. Sherer, E. Mills, and B. Leuner, The effects of gestational stress and Selective Serotonin reuptake inhibitor antidepressant treatment on structural plasticity in the postpartum brain--A translational model for postpartum depression, Horm Behav, vol.77, pp.124-155, 2016.

R. D. Porsolt, G. Brossard, C. Hautbois, and S. Roux, Rodent models of depression: forced swimming and tail suspension behavioral despair tests in rats and mice, Curr Protoc Neurosci Chapter, vol.8, p.10, 2001.

C. V. Perani and D. A. Slattery, Using animal models to study post-partum psychiatric disorders, Br J Pharmacol, vol.171, pp.4539-55, 2014.

L. L. Howell and K. A. Cunningham, Serotonin 5-HT2 receptor interactions with dopamine function: implications for therapeutics in cocaine use disorder, Pharmacol Rev, vol.67, pp.176-97, 2015.

R. S. Bridges, Neuroendocrine regulation of maternal behavior, Front Neuroendocrinol, vol.36, pp.178-96, 2015.

C. L. Bethea, M. Pecins-thompson, W. E. Schutzer, C. Gundlah, and Z. N. Lu, Ovarian steroids and serotonin neural function, Mol Neurobiol, vol.18, pp.87-123, 1998.

O. T. Hernandez-hernandez, L. Martinez-mota, J. J. Herrera-perez, and G. Jimenez-rubio, Role of estradiol in the expression of genes involved in serotonin neurotransmission: Implications for female depression, Curr Neuropharmacol, 2018.

J. Barnes, V. Mondelli, and C. M. Pariante, Genetic Contributions of Inflammation to Depression, Neuropsychopharmacology, vol.42, pp.81-98, 2017.

A. Haim, D. Julian, C. Albin-brooks, H. M. Brothers, K. M. Lenz et al., A survey of neuroimmune changes in pregnant and postpartum female rats, Brain Behav Immun, vol.59, 2017.

, Rat GD15: ?pup licking, ?hovering over, ?maternal aggression PD2: ?pup licking, ?kyphosis, ?supine nursing ?maternal aggression Holschbach, 2018.