When becoming a parent, caregivers undergo complex, and sometimes permanent, neurobiological alterations, and this area of neurobiology has been extensively studied for decades. Due to ethical concerns and experimental limitations, the first parental neurobiology experiments were exclusively performed using rodent animal model systems, such as mice, rats, and voles. More recent technological advancements, such as the functional MRI (fMRI) scan, have become widely adopted and led to great insight into the impact of parenting on human neurobiology. In this thematic literature review, we present key studies that provide insight into the relationship of pregnancy and parturition on maternal caregiving behavior and the relationship of postpartum on all parents. First, we examine the relationship of endocrine hormones such as estrogen, progesterone, oxytocin, and testosterone with the neurobiological development of a parent. Next, we describe the significant transformation of subcortical maternal circuit components that occur during pregnancy, and the changes in the volume of grey and white matter generated during the postpartum. These brain structure alterations contribute to the development of parental nurturing behaviors.
Citation: Elaine K. Feller, Erin N. McGinity, Patrick William Cafferty. Hormonal and structural transformations in the caregiver's brain: Examining themes in parental neurobiology[J]. AIMS Neuroscience, 2025, 12(4): 614-634. doi: 10.3934/Neuroscience.2025030
When becoming a parent, caregivers undergo complex, and sometimes permanent, neurobiological alterations, and this area of neurobiology has been extensively studied for decades. Due to ethical concerns and experimental limitations, the first parental neurobiology experiments were exclusively performed using rodent animal model systems, such as mice, rats, and voles. More recent technological advancements, such as the functional MRI (fMRI) scan, have become widely adopted and led to great insight into the impact of parenting on human neurobiology. In this thematic literature review, we present key studies that provide insight into the relationship of pregnancy and parturition on maternal caregiving behavior and the relationship of postpartum on all parents. First, we examine the relationship of endocrine hormones such as estrogen, progesterone, oxytocin, and testosterone with the neurobiological development of a parent. Next, we describe the significant transformation of subcortical maternal circuit components that occur during pregnancy, and the changes in the volume of grey and white matter generated during the postpartum. These brain structure alterations contribute to the development of parental nurturing behaviors.
| [1] |
Feldman R (2015) The adaptive human parental brain: Implications for children's social development. Trends Neurosci 38: 387-399. https://doi.org/10.1016/j.tins.2015.04.004
|
| [2] |
Trainor BC, Bird IM, Alday NA, et al. (2003) Variation in aromatase activity in the medial preoptic area and plasma progesterone is associated with the onset of paternal behavior. Neuroendocrinology 78: 36-44. https://doi.org/10.1159/000071704
|
| [3] |
Pal T, McQuillan HJ, Wragg L, et al. (2025) Hormonal actions in the medial preoptic area governing parental behavior: Novel insights from new tools. Endocrinology 166: bqae152. https://doi.org/10.1210/endocr/bqae152
|
| [4] |
Hoekzema E, Tamnes CK, Berns P, et al. (2020) Becoming a mother entails anatomical changes in the ventral striatum of the human brain that facilitate its responsiveness to offspring cues. Psychoneuroendocrinology 112: 104507. https://doi.org/10.1016/j.psyneuen.2019.104507
|
| [5] |
Rilling JK (2024) Father nature: The science of paternal potential. Cambridge (MA): MIT Press. Chapter 2, Transformations. https://doi.org/10.7551/mitpress/14599.003.0005
|
| [6] |
Numan M (2020) The parental brain mechanisms, development, and evolution. New York: Oxford University Press. General conclusions; p. 50–51. https://doi.org/10.1093/oso/9780190848675.001.0001
|
| [7] |
Carollo A, Torre L, Bornstein MH, et al. (2025) The parental brain: Anatomization of 75 years of neuroscience 1951–2024. Neurosci Res 216: 104890-104896. https://doi.org/10.1016/j.neures.2025.03.002
|
| [8] |
Kim P, Rigo P, Mayes LC, et al. (2014) Neural plasticity in fathers of human infants. Soc Neurosci 9: 522-535. https://doi.org/10.1080/17470919.2014.933713
|
| [9] |
Dudas A, Nakahara TS, Pellissier LP, et al. (2024) Parenting behaviors in mice: Olfactory mechanisms and features in models of autism spectrum disorders. Neurosci Biobehav Rev 161: 105686-105688. https://doi.org/10.1016/j.neubiorev.2024.105686
|
| [10] |
Moltz H, Lubin M, Leon M, et al. (1970) Hormonal induction of maternal behavior in the ovariectomized nulliparous rat. Physiol Behav 5: 1373-1377. https://doi.org/10.1016/0031-9384(70)90122-8
|
| [11] |
Lubin M (1972) Hormones and maternal behavior in the male rat. Horm Behav 3: 369-374. https://doi.org/10.1016/0018-506x(72)90026-8
|
| [12] |
Siegel HI, Rosenblatt JS (1975) Progesterone inhibition of estrogen-induced maternal behavior in hysterectomized-ovariectomized virgin rats. Horm Behav 6: 223-230. https://doi.org/10.1016/0018-506x(75)90009-4
|
| [13] |
Smith MS, Neill JD (1977) Inhibition of gonadotropin secretion during lactation in the rat: Relative contribution of suckling and ovarian steroids. Biol Reprod 17: 255-261. https://doi.org/10.1095/biolreprod17.2.255
|
| [14] |
Numan M (1978) Progesterone inhibition of maternal behavior in the rat. Horm Behav 11: 209-231. https://doi.org/10.1016/0018-506x(78)90050-8
|
| [15] |
Olazábal DE, Pereira M, Agrati D, et al. (2013) Flexibility and adaptation of the neural substrate that supports maternal behavior in mammals. Neurosci Biobehav Rev 37: 1875-1892. https://doi.org/10.1016/j.neubiorev.2013.04.004
|
| [16] |
Olazábal DE, Pereira M, Agrati D, et al. (2013) New theoretical and experimental approaches on maternal motivation in mammals. Neurosci Biobehav Rev 37: 1860-1874. https://doi.org/10.1016/j.neubiorev.2013.04.003
|
| [17] |
Martín-Sánchez A, Valera-Marín G, Hernández-Martínez A, et al. (2015) Wired for motherhood: Induction of maternal care but not maternal aggression in virgin female CD1 mice. Front Behav Neurosci 9: 197. https://doi.org/10.3389/fnbeh.2015.00197
|
| [18] |
Numan M (1974) Medial preoptic area and maternal behavior in the female rat. J Comp Psychol 87: 746-759. https://doi.org/10.1037/h0036974
|
| [19] |
Numan M (2020) The parental brain: mechanisms, development, and evolution. New York: Oxford University Press. Chapter 5, Central neural circuits regulating maternal behavior in nonhuman mammals; p. 99–163. https://doi.org/10.1093/oso/9780190848675.003.0005
|
| [20] |
Numan M, Rosenblatt JS, Komisaruk BR (1977) Medial preoptic area and onset of maternal behavior in the rat. J Comp Physiol Psychol 91: 146-164. https://doi.org/10.1037/h0077304
|
| [21] |
Ogawa S, Eng V, Taylor J, et al. (1998) Roles of estrogen receptor-alpha gene expression in reproduction-related behaviors in female mice. Endocrinol 139: 5070-5081. https://doi.org/10.1210/endo.139.12.6357
|
| [22] |
Ribeiro AC, Musatov S, Shteyler A, et al. (2012) siRNA silencing of estrogen receptor-α expression specifically in medial preoptic area neurons abolishes maternal care in female mice. Proc Natl Acad Sci USA 109: 16324-16329. https://doi.org/10.1073/pnas.1214094109
|
| [23] |
Ammari R, Monaca F, Cao M, et al. (2023) Hormone-mediated neural remodeling orchestrates parenting onset during pregnancy. Science 382: 76-81. https://doi.org/10.1126/science.adi0576
|
| [24] |
Fang YY, Yamaguchi T, Song SC, et al. (2018) A hypothalamic midbrain pathway essential for driving maternal behaviors. Neuron 98: 192-207. https://doi.org/10.1016/j.neuron.2018.02.019
|
| [25] |
Sheehan T, Numan M (2002) Estrogen, progesterone, and pregnancy termination alter neural activity in brain regions that control maternal behavior in rats. Neuroendocrinology 75: 12-23. https://doi.org/10.1159/000048217
|
| [26] |
Wang MW, Crombie DL, Hayes JS, et al. (1995) Aberrant maternal behaviour in mice treated with a progesterone receptor antagonist during pregnancy. J Endocrinol 145: 371-377. https://doi.org/10.1677/joe.0.1450371
|
| [27] |
Bridges RS, Rosenblatt JS, Feder HH (1978) Serum progesterone concentrations and maternal behavior in rats after pregnancy termination: Behavioral stimulation after progesterone withdrawal and inhibition by progesterone maintenance. Endocrinology 102: 258-267. https://doi.org/10.1210/endo-102-1-258
|
| [28] |
Tsuneoka Y, Yoshihara C, Ohnishi R, et al. (2022) Oxytocin facilitates allomaternal behavior under stress in laboratory mice. eNeuro 9: 405-409. https://doi.org/10.1523/ENEURO.0405-21.2022
|
| [29] | Hidema S, Sato K, Mizukami H, et al. (2024) Oxytocin receptor-expressing neurons in the medial preoptic area are essential for lactation, whereas those in the lateral septum are not critical for maternal behavior. Endocrinology 114: 517-537. https://doi.org/10.1159/000535362 |
| [30] |
Bales KL, Saltzman W (2017) Fathering in rodents: Neurobiological substrates and consequences for offspring. Horm Behav 77: 249-259. https://doi.org/10.1016/j.yhbeh.2015.05.021
|
| [31] |
Numan M, Roach JK, Cerro D, et al. (1999) Expression of intracellular progesterone receptors in rat brain during different reproductive states, and involvement in maternal behavior. Brain Res 830: 358-371. https://doi.org/10.1016/s0006-8993(99)01424-9
|
| [32] |
Hyer MM, Khantsis S, Venezia C, et al. (2017) Estrogen-dependent modifications to hippocampal plasticity in paternal California mice (Peromyscus californicus). Horm Behav 96: 147-155. https://doi.org/10.1016/j.yhbeh.2017.09.015
|
| [33] |
Schneider JS, Burgess C, Horton TH, et al. (2009) Effects of progesterone on male-mediated infant-directed aggression. Behav Brain Res 199: 340-344. https://doi.org/10.1016/j.bbr.2008.12.019
|
| [34] |
Hume JM, Wynne-Edwards KE (2005) Castration reduces male testosterone, estradiol, and territorial aggression, but not paternal behavior in biparental dwarf hamsters (Phodopus campbelli). Horm Behav 48: 303-310. https://doi.org/10.1016/j.yhbeh.2005.04.001
|
| [35] |
Trainor BC, Marler CA (2001) Testosterone, paternal behavior, and aggression in the monogamous California mouse (Peromyscus californicus). Horm Behav 40: 32-42. https://doi.org/10.1006/hbeh.2001.1652
|
| [36] |
Duarte-Guterman P, Skandalis DA, Merkl A, et al. (2025) Brain aromatase and its relationship with parental experience and behavior in male mice. Front Neurosci 19: 1502764. https://doi.org/10.3389/fnins.2025.1502764
|
| [37] |
Yuan W, He Z, Hou W, et al. (2019) Role of oxytocin in the medial preoptic area (MPOA) in the modulation of paternal behavior in mandarin voles. Horm Behav 110: 46-55. https://doi.org/10.1016/j.yhbeh.2019.02.014
|
| [38] |
Perea-Rodriguez JP, Takahashi EY, Amador TM, et al. (2015) Effects of reproductive experience on central expression of progesterone, oestrogen α, oxytocin and vasopressin receptor mRNA in male California mice (Peromyscus californicus). J Neuroendocrinol 27: 245-252. https://doi.org/10.1111/jne.12264
|
| [39] |
Stolzenberg DS, Rissman EF (2011) Oestrogen-independent, experience-induced maternal behaviour in female mice. J Neuroendocrinol 23: 345-354. https://doi.org/10.1111/j.1365-2826.2011.02112.x
|
| [40] |
Numan M (2006) Motivational systems and the neural circuitry of maternal behavior in the rat. Dev Psychobiol 49: 12-21. https://doi.org/10.1002/dev.20198
|
| [41] |
de Sousa FL, Lazzari V, de Azevedo MS, et al. (2010) Progesterone and maternal aggressive behavior in rats. Behav Brain Res 212: 84-9. https://doi.org/10.1016/j.bbr.2010.03.050
|
| [42] |
Grieb ZA, Tierney SM, Lonstein JS (2017) Postpartum inhibition of ovarian steroid action increases aspects of maternal caregiving and reduces medial preoptic area l receptor expression in female rats. Horm Behav 96: 31-41. https://doi.org/10.1016/j.yhbeh.2017.08.007
|
| [43] |
Lovick TA, Zangrossi H (2021) Effect of estrous cycle on behavior of females in rodent tests of anxiety. Front Psychiatry 12: 711065. https://doi.org/10.3389/fpsyt.2021.711065
|
| [44] |
Gilbert AN (1984) Postpartum and lactational estrus: A comparative analysis in rodentia. J Comp Psychol 98: 232-245. https://doi.org/10.1037//0735-7036.98.3.232
|
| [45] | Dewan ZF, Morris ID, Lendon RG (2000) Administration of exogenous testosterone in the adult rat and its effects on reproductive organs, sex hormones and body-weight. Bangladesh Med Res Counc Bull 26: 48-55. |
| [46] |
Albert DJ, Walsh ML, Gorzalka BB, et al. (1986) Testosterone removal in rats results in a decrease in social aggression and a loss of social dominance. Physiol Behav 36: 401-407. https://doi.org/10.1016/0031-9384(86)90305-7
|
| [47] |
Batrinos ML (2012) Testosterone and aggressive behavior in man. Int J Endocrinol Metab 10: 563-568. https://doi.org/10.5812/ijem.3661
|
| [48] |
Kelly AM, Thompson RR (2023) Testosterone facilitates nonreproductive, context-appropriate pro- and anti-social behavior in female and male Mongolian gerbils. Horm Behav 156: 105436-105436. https://doi.org/10.1016/j.yhbeh.2023.105436
|
| [49] |
Gettler LT, Ryan CP, Eisenberg DT, et al. (2017) The role of testosterone in coordinating male life history strategies: The moderating effects of the androgen receptor CAG repeat polymorphism. Horm Behav 87: 164-175. https://doi.org/10.1016/j.yhbeh.2016.10.012
|
| [50] |
Rilling JK (2024) Father nature: The science of paternal potential. Cambridge (MA): MIT Press. Chapter 3, Testosterone; p. 99–136. https://doi.org/10.7551/mitpress/14599.003.0006
|
| [51] |
Pawluski JL (2024) The parental brain, perinatal mental illness, and treatment: A review of key structural and functional changes. Semin Perinatol 48: 151951. https://doi.org/10.1016/j.semperi.2024.151951
|
| [52] |
Rotondi V, Allegra M, Kashyap R, et al. (2024) Enduring maternal brain changes and their role in mediating motherhood's impact on well-being. Sci Rep 14: 16608. https://doi.org/10.1038/s41598-024-67316-y
|
| [53] |
Swain JE (2011) The human parental brain: In vivo neuroimaging. Prog Neuropsychopharmacol Biol Psychiatry 35: 1242-1254. https://doi.org/10.1016/j.pnpbp.2010.10.017
|
| [54] |
Pawluski JL, Lambert KG, Kinsley CH (2016) Neuroplasticity in maternal hippocampus: Relation to cognition and effects of repeated stress. Horm Behav 77: 86-97. https://doi.org/10.1016/j.yhbeh.2015.06.004
|
| [55] |
Numan M (1988) Neural basis of maternal behavior in the rat. Psychoneuroendocrinology 13: 47-62. https://doi.org/10.1016/0306-4530(88)90006-6
|
| [56] |
Li M (2020) Psychological and neurobiological mechanisms underlying the decline of maternal behavior. Neurosci Biobehav Rev 116: 164-181. https://doi.org/10.1016/j.neubiorev.2020.06.009
|
| [57] |
Swain JE, Konrath S, Brown SL, et al. (2013) Parenting and beyond: Common neurocircuits underlying parental and altruistic care. Parent Sci Pract 12: 115-123. https://doi.org/10.1080/15295192.2012.680409
|
| [58] |
Kuroda KO, Fukumitsu K, Kurachi T, et al. (2024) Parental brain through time: The origin and development of the neural circuit of mammalian parenting. Ann N Y Acad Sci 1534: 24-44. https://doi.org/10.1111/nyas.15111
|
| [59] |
Barrière DA, Ella A, Szeremeta F, et al. (2021) Brain orchestration of pregnancy and maternal behavior in mice: A longitudinal morphometric study. Neuroimage 230: 117776. http://doi.org/10.1016/j.neuroimage.2021.117776
|
| [60] |
Mulligan EM, Low M, Flynn H, et al. (2021) The rewards of motherhood: Neural response to reward in pregnancy prospectively predicts maternal bonding with the infant in the postpartum period. Biol Psychol 163: 108148. https://doi.org/10.1016/j.biopsycho.2021.108148
|
| [61] |
Li M, Fleming AS (2003) The nucleus accumbens shell is critical for normal expression of pup-retrieval in postpartum female rats. Behav Brain Res 145: 99-111. https://doi.org/10.1016/S0166-4328(03)00135-9
|
| [62] |
Mannella F, Gurney K, Baldassarre G (2013) The nucleus accumbens as a nexus between values and goals is goal-directed behavior: A review and new hypothesis. Front Behav Neurosci 7: 135. https://doi.org/10.3389/fnbeh.2013.00135
|
| [63] |
Orchard ER, Voigt K, Chopra S, et al. (2023) The maternal brain is more flexible and responsive at rest: Effective connectivity of the parental caregiving network in postpartum mothers. Sci Rep 13: 4719. https://doi.org/10.1038/s41598-023-31696-4
|
| [64] |
Stewart DE, Vigod S (2016) Postpartum depression. N Engl J Med 375: 2177-2186. https://doi.org/10.1056/NEJMcp1607649
|
| [65] |
Howard LM, Molyneaux E, Dennis CL, et al. (2014) Non-psychotic mental disorders in the perinatal period. Lancet 384: 1775-1788. https://doi.org/10.1016/S0140-6736(14)61276-9
|
| [66] |
Pawluski JL, Lonstein JS, Fleming AS (2017) The neurobiology of postpartum anxiety and depression. Trends Neurosci 40: 106-120. https://doi.org/10.1016/j.tins.2016.11.009
|
| [67] |
Pereira M (2016) Structural and functional plasticity in the maternal brain circuitry. New Dir Child Adolesc Dev 2016: 23-46. https://doi.org/10.1002/cad.20163
|
| [68] |
Barba-Muller E, Craddock S, Carmona S (2019) Brain plasticity in pregnancy and the postpartum period: Links to maternal caregiving and mental health. Arch Womens Ment Health 22: 289-299. https://doi.org/10.1007/s00737-018-0889-z
|
| [69] |
Lee A, Li M, Watchus J, et al. (1999) Neuroanatomical basis of maternal memory in postpartum rats: Selective role for the nucleus accumbens. Behav Neurosci 113: 523-538. https://doi.org/10.1037//0735-7044.113.3.523
|
| [70] |
Kim P, Leckman JF, Mayes LC, et al. (2010) The plasticity of human maternal brain: Longitudinal changes in brain anatomy during the early postpartum period. Behav Neurosci 124: 695-700. https://doi.org/10.1037/a0020884
|
| [71] |
Luders E, Gaser C, Gingnell M, et al. (2021) Significant increases of the amygdala between immediate and late postpartum: Pronounced effects within the superficial subregion. J Neurosci Res 99: 2261-2270. https://doi.org/10.1002/jnr.24855
|
| [72] |
Matsuda KI, Tanaka M (2025) Changes in estrogen receptor α positive cells in the amygdala and bed nucleus of the stria terminalis during pregnancy and the postpartum period in rats. Histochem Cell Biol 163: 47. https://doi.org/10.1007/s00418-025-02376-3
|
| [73] |
Ballesteros C, Paternina-Die M, Martinez-Garcia M, et al. (2025) Linking birth experience and perinatal depression symptoms to neuroanatomical changes in hippocampus and amygdala. Sci Adv 11: eadt5619. https://doi.org/10.1126/sciadv.adt5619
|
| [74] |
Mao N, Che K, Xie H, et al. (2020) Abnormal information flow in postpartum depression: A resting-state functional magnetic resonance imaging study. J Affect Disord 277: 596-602. https://doi.org/10.1016/j.jad.2020.08.060
|
| [75] |
Chase HW, Moses-Kolko EL, Zevallos C, et al. (2014) Disrupted posterior cingulate-amygdala connectivity in postpartum depressed women as measured with resting BOLD fMRI. Soc Cogn Affect Neurosci 9: 1069-75. https://doi.org/10.1093/scan/nst083
|
| [76] |
Khadka N, Fassett MJ, Oyelese Y, et al. (2024) Trends in postpartum depression by race, ethnicity, and prepregnancy body mass index. JAMA Netw Open 7: e2446486. https://doi.org/10.1001/jamanetworkopen.2024.46486
|
| [77] | Wan L, Tu T, Zhang QL, et al. (2019) Pregnancy promotes maternal hippocampal neurogenesis in guinea pigs. Neural Plast 2019: 5765284. https://doi.org/10.1155/2019/5765284 |
| [78] |
Leuner B, Mirescu C, Noiman L, et al. (2007) Maternal experience inhibits the production of immature neurons in the hippocampus during the postpartum period through elevations in adrenal steroids. Hippocampus 17: 434-442. https://doi.org/10.1002/hipo.20278
|
| [79] |
Rolls A, Schori H, London A, et al. (2008) Decrease in hippocampal neurogenesis during pregnancy: A link to immunity. Mol Psychiatry 13: 468-469. https://doi.org/10.1038/sj.mp.4002126
|
| [80] |
Spritzer MD, Panning AW, Engelman SM, et al. (2017) Seasonal and sex differences in cell proliferation, neurogenesis, and cell death within the dentate gyrus of adult wild-caught meadow voles. Neurosci 360: 155-165. https://doi.org/10.1016/j.neuroscience.2017.07.046
|
| [81] |
Farrar VS, Gallardo JM, Calisi RM (2022) Prior parental experience attenuates hormonal stress responses and alters hippocampal glucocorticoid receptors in biparental rock doves. J Exp Biol 225: jeb244820. https://doi.org/10.1242/jeb.244820
|
| [82] |
Moses-Kolko EL, Banihashemi L, Hipwell AE (2021) Reduced postpartum hippocampal volume is associated with positive mother-infant caregiving behavior. J Affect Disord 281: 297-302. https://doi.org/10.1016/j.jad.2020.12.014
|
| [83] |
Hoekzema E, van Steenbergen H, Straathof M, et al. (2022) Mapping the effects of pregnancy on resting state brain activity, white matter microstructure, neural metabolite concentrations and grey matter architecture. Nat Commun 13: 6931. https://doi.org/10.1038/s41467-022-33884-8
|
| [84] |
Saxbe D, Martínez-Garcia M, Cardenas SI, et al. (2023) Changes in left hippocampal volume in first-time fathers: Association with oxytocin, testosterone, and adaptation to parenthood. J Neuroendocrinol 35: e13270. https://doi.org/10.1111/jne.13270
|
| [85] |
Pritschet L, Taylor CM, Cossio D, et al. (2024) Neuroanatomical changes observed over the course of a human pregnancy. Nat Neurosci 27: 2253-2260. https://doi.org/10.1038/s41593-024-01741-0
|
| [86] |
Servin-Barthet C, Martínez-García M, Paternina-Die M, et al. (2025) Pregnancy entails a U-shaped trajectory in human brain structure linked to hormones and maternal attachment. Nat Commun 16: 730. https://doi.org/10.1038/s41467-025-55830-0
|
| [87] |
Kim P, Dufford AJ, Tribble RC (2018) Cortical thickness variation of the maternal brain in the first 6 months postpartum: Associations with parental self-efficacy. Brain Struct Funct 223: 3267-3277. https://doi.org/10.1007/s00429-018-1688-z
|
| [88] |
Abraham E, Hendler T, Shapira-Lichter I, et al. (2014) Father's brain is sensitive to childcare experiences. Proc Natl Acad Sci USA 111: 9792-9797. https://doi.org/10.1073/pnas.1402569111
|
| [89] |
Cárdenas SI, Waizman Y, Truong V, et al. (2024) White matter microstructure organization across the transition to fatherhood. Dev Cogn Neurosci 67: 101374. http://doi.org/10.1016/j.dcn.2024.101374
|
| [90] |
Giannotti M, Gemignani M, Rigo P, et al. (2022) Disentangling the effect of sex and caregiving role: The investigation of male same-sex parents as an opportunity to learn more about the neural parental caregiving network. Front Psychol 13: 842361. https://doi.org/10.3389/fpsyg.2022.842361
|
| [91] |
Orchard ER, Ward PGD, Sforazzini F, et al. (2020) Relationship between parenthood and cortical thickness in late adulthood. PLoS One 15: e0236031. https://doi.org/10.1371/journal.pone.0236031
|
| [92] |
Keyser-Marcus L, Stafisso-Sandoz G, Gerecke K, et al. (2001) Alteration in the medial preoptic area following pregnancy and pregnancy-like steroidal treatment in the rat. Brain Res Bull 55: 737-745. https://doi.org/10.1016/S0361-9230(01)00554-8
|
| [93] |
Lee A, Clancy S, Fleming AS (2000) Mother rats bar-press for pups: Effects of lesions of the mpoa and limbic sites on maternal behavior and operant responding for pup-reinforcement. Behav Brain Res 108: 215-231. https://doi.org/10.1016/S0166-4328(99)00170-9
|
| [94] |
Nehls S, Losse E, Enzensberger C, et al. (2024) Time-sensitive changes in the maternal brain and their influence on mother-child attachment. Transl Psychiatry 14: 84. https://doi.org/10.1038/s41398-024-02805-2
|
| [95] |
Atzil S, Hendler T, Zagoory-Sharon O, et al. (2012) Synchrony and specificity in the maternal and paternal brain: Relations to oxytocin and vasopressin. J Am Acad Child Adolesc Psychiatry 51: 798-881. https://doi.org/10.1016/j.jaac.2012.06.008
|
| [96] |
Ho SS, Swain JE (2017) Depression alters maternal extended amygdala response and functional connectivity during distress signals in attachment relationship. Behav Brain Res 325: 290-296. https://doi.org/10.1016/j.bbr.2017.02.045
|
| [97] |
Orchard ER, Chopra S, Ooi LQR, et al. (2025) Protective role of parenthood on age-related brain function in mid- to late-life. Proc Natl Acad Sci USA 122: e2411245122. https://doi.org/10.1073/pnas.2411245122
|