Differential Methylation of Genes in the Medial Prefrontal Cortex of Developing and Adult Rats Following Exposure to Maltreatment or Nurturing Care During Infancy
Quality of maternal care in infancy is an important contributing factor in the development of behavior and psychopathology. One way maternal care could affect behavioral trajectories is through environmentally induced epigenetic alterations within brain regions known to play prominent roles in cogni...
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Published in | Developmental neuroscience Vol. 35; no. 4; pp. 306 - 316 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Basel, Switzerland
S. Karger AG
01.01.2013
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Subjects | |
Online Access | Get full text |
ISSN | 0378-5866 1421-9859 1421-9859 |
DOI | 10.1159/000350716 |
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Abstract | Quality of maternal care in infancy is an important contributing factor in the development of behavior and psychopathology. One way maternal care could affect behavioral trajectories is through environmentally induced epigenetic alterations within brain regions known to play prominent roles in cognition, emotion regulation, and stress responsivity. Whereas such research has largely focused on the hippocampus or hypothalamus, the prefrontal cortex (PFC) has only just begun to receive attention. The current study was designed to determine whether exposure to maltreatment or nurturing care is associated with differential methylation of candidate gene loci (bdnf and reelin) within the medial PFC (mPFC) of developing and adult rats. Using a within-litter design, infant male and female rats were exposed to an adverse or nurturing caregiving environment outside their home cage for 30 min per day during the first postnatal week. Additional littermates remained with their biological caregiver within the home cage during the manipulations. We observed that infant rats subjected to caregiver maltreatment emitted more audible and ultrasonic vocalizations than littermates subjected to nurturing care either within or outside of the home cage. While we found no maltreatment-induced changes in bdnf DNA methylation present in infancy, sex-specific alterations were present in the mPFC of adolescents and adults that had been exposed to maltreatment. Furthermore, while maltreated females showed differences in reelin DNA methylation that were transient, males exposed to maltreatment and both males and females exposed to nurturing care outside the home cage showed differences in reelin methylation that emerged by adulthood. Our results demonstrate the ability of infant-caregiver interactions to epigenetically mark genes known to play a prominent role in cognition and psychiatric disorders within the mPFC. Furthermore, our data indicate the remarkable complexity of alterations that can occur, with both transient and later emerging DNA methylation differences that could shape developmental trajectories and underlie gender differences in outcomes. |
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AbstractList | Quality of maternal care in infancy is an important contributing factor in the development of behavior and psychopathology. One way maternal care could affect behavioral trajectories is through environmentally induced epigenetic alterations within brain regions known to play prominent roles in cognition, emotion regulation, and stress responsivity. Whereas such research has largely focused on the hippocampus or hypothalamus, the prefrontal cortex (PFC) has only just begun to receive attention. The current study was designed to determine whether exposure to maltreatment or nurturing care is associated with differential methylation of candidate gene loci (bdnf and reelin) within the medial PFC (mPFC) of developing and adult rats. Using a within-litter design, infant male and female rats were exposed to an adverse or nurturing caregiving environment outside their home cage for 30 min per day during the first postnatal week. Additional littermates remained with their biological caregiver within the home cage during the manipulations. We observed that infant rats subjected to caregiver maltreatment emitted more audible and ultrasonic vocalizations than littermates subjected to nurturing care either within or outside of the home cage. While we found no maltreatment-induced changes in bdnf DNA methylation present in infancy, sex-specific alterations were present in the mPFC of adolescents and adults that had been exposed to maltreatment. Furthermore, while maltreated females showed differences in reelin DNA methylation that were transient, males exposed to maltreatment and both males and females exposed to nurturing care outside the home cage showed differences in reelin methylation that emerged by adulthood. Our results demonstrate the ability of infant-caregiver interactions to epigenetically mark genes known to play a prominent role in cognition and psychiatric disorders within the mPFC. Furthermore, our data indicate the remarkable complexity of alterations that can occur, with both transient and later emerging DNA methylation differences that could shape developmental trajectories and underlie gender differences in outcomes.Quality of maternal care in infancy is an important contributing factor in the development of behavior and psychopathology. One way maternal care could affect behavioral trajectories is through environmentally induced epigenetic alterations within brain regions known to play prominent roles in cognition, emotion regulation, and stress responsivity. Whereas such research has largely focused on the hippocampus or hypothalamus, the prefrontal cortex (PFC) has only just begun to receive attention. The current study was designed to determine whether exposure to maltreatment or nurturing care is associated with differential methylation of candidate gene loci (bdnf and reelin) within the medial PFC (mPFC) of developing and adult rats. Using a within-litter design, infant male and female rats were exposed to an adverse or nurturing caregiving environment outside their home cage for 30 min per day during the first postnatal week. Additional littermates remained with their biological caregiver within the home cage during the manipulations. We observed that infant rats subjected to caregiver maltreatment emitted more audible and ultrasonic vocalizations than littermates subjected to nurturing care either within or outside of the home cage. While we found no maltreatment-induced changes in bdnf DNA methylation present in infancy, sex-specific alterations were present in the mPFC of adolescents and adults that had been exposed to maltreatment. Furthermore, while maltreated females showed differences in reelin DNA methylation that were transient, males exposed to maltreatment and both males and females exposed to nurturing care outside the home cage showed differences in reelin methylation that emerged by adulthood. Our results demonstrate the ability of infant-caregiver interactions to epigenetically mark genes known to play a prominent role in cognition and psychiatric disorders within the mPFC. Furthermore, our data indicate the remarkable complexity of alterations that can occur, with both transient and later emerging DNA methylation differences that could shape developmental trajectories and underlie gender differences in outcomes. Quality of maternal care in infancy is an important contributing factor in the development of behavior and psychopathology. One way maternal care could affect behavioral trajectories is through environmentally induced epigenetic alterations within brain regions known to play prominent roles in cognition, emotion regulation, and stress responsivity. Whereas such research has largely focused on the hippocampus or hypothalamus, the prefrontal cortex (PFC) has only just begun to receive attention. The current study was designed to determine whether exposure to maltreatment or nurturing care is associated with differential methylation of candidate gene loci (bdnf and reelin) within the medial PFC (mPFC) of developing and adult rats. Using a within-litter design, infant male and female rats were exposed to an adverse or nurturing caregiving environment outside their home cage for 30 min per day during the first postnatal week. Additional littermates remained with their biological caregiver within the home cage during the manipulations. We observed that infant rats subjected to caregiver maltreatment emitted more audible and ultrasonic vocalizations than littermates subjected to nurturing care either within or outside of the home cage. While we found no maltreatment-induced changes in bdnf DNA methylation present in infancy, sex-specific alterations were present in the mPFC of adolescents and adults that had been exposed to maltreatment. Furthermore, while maltreated females showed differences in reelin DNA methylation that were transient, males exposed to maltreatment and both males and females exposed to nurturing care outside the home cage showed differences in reelin methylation that emerged by adulthood. Our results demonstrate the ability of infant-caregiver interactions to epigenetically mark genes known to play a prominent role in cognition and psychiatric disorders within the mPFC. Furthermore, our data indicate the remarkable complexity of alterations that can occur, with both transient and later emerging DNA methylation differences that could shape developmental trajectories and underlie gender differences in outcomes. Quality of maternal care in infancy is an important contributing factor in the development of behavior and psychopathology. One way maternal care could affect behavioral trajectories is through environmentally induced epigenetic alterations within brain regions known to play prominent roles in cognition, emotion regulation, and stress responsivity. Whereas such research has largely focused on the hippocampus or hypothalamus, the prefrontal cortex (PFC) has only just begun to receive attention. The current study was designed to determine whether exposure to maltreatment or nurturing care is associated with differential methylation of candidate gene loci (bdnf and reelin) within the medial PFC (mPFC) of developing and adult rats. Using a within-litter design, infant male and female rats were exposed to an adverse or nurturing caregiving environment outside their home cage for 30 min per day during the first postnatal week. Additional littermates remained with their biological caregiver within the home cage during the manipulations. We observed that infant rats subjected to caregiver maltreatment emitted more audible and ultrasonic vocalizations than littermates subjected to nurturing care either within or outside of the home cage. While we found no maltreatment-induced changes in bdnf DNA methylation present in infancy, sex-specific alterations were present in the mPFC of adolescents and adults that had been exposed to maltreatment. Furthermore, while maltreated females showed differences in reelin DNA methylation that were transient, males exposed to maltreatment and both males and females exposed to nurturing care outside the home cage showed differences in reelin methylation that emerged by adulthood. Our results demonstrate the ability of infant-caregiver interactions to epigenetically mark genes known to play a prominent role in cognition and psychiatric disorders within the mPFC. Furthermore, our data indicate the remarkable complexity of alterations that can occur, with both transient and later emerging DNA methylation differences that could shape developmental trajectories and underlie gender differences in outcomes. Copyright © 2013 S. Karger AG, Basel [PUBLICATION ABSTRACT] Quality of maternal care in infancy is an important contributing factor in the development of behavior and psychopathology. One way maternal care could affect behavioral trajectories is through environmentally induced epigenetic alterations within brain regions known to play prominent roles in cognition, emotion regulation, and stress responsivity. Whereas such research has largely focused on the hippocampus or hypothalamus, the prefrontal cortex (PFC) has only just begun to receive attention. The current study was designed to determine whether exposure to maltreatment or nurturing care is associated with differential methylation of candidate gene loci (bdnf and reelin) within the medial PFC (mPFC) of developing and adult rats. Using a within-litter design, infant male and female rats were exposed to an adverse or nurturing caregiving environment outside their home cage for 30 min per day during the first postnatal week. Additional littermates remained with their biological caregiver within the home cage during the manipulations. We observed that infant rats subjected to caregiver maltreatment emitted more audible and ultrasonic vocalizations than littermates subjected to nurturing care either within or outside of the home cage. While we found no maltreatment-induced changes in bdnf DNA methylation present in infancy, sex-specific alterations were present in the mPFC of adolescents and adults that had been exposed to maltreatment. Furthermore, while maltreated females showed differences in reelin DNA methylation that were transient, males exposed to maltreatment and both males and females exposed to nurturing care outside the home cage showed differences in reelin methylation that emerged by adulthood. Our results demonstrate the ability of infant-caregiver interactions to epigenetically mark genes known to play a prominent role in cognition and psychiatric disorders within the mPFC. Furthermore, our data indicate the remarkable complexity of alterations that can occur, with both transient and later emerging DNA methylation differences that could shape developmental trajectories and underlie gender differences in outcomes. Copyright copyright 2013 S. Karger AG, Basel Quality of maternal care in infancy is an important contributing factor in the development of behavior and psychopathology. One way maternal care could affect behavioral trajectories is through environmentally-induced epigenetic alterations within brain regions known to play prominent roles in cognition, emotion regulation, and stress responsivity. Whereas such research has largely focused on the hippocampus or hypothalamus, the prefrontal cortex (PFC) has only begun to receive attention. The current study was designed to determine whether exposure to maltreatment or nurturing care is associated with differential methylation of candidate gene loci ( bdnf and reelin ) within the medial PFC (mPFC) of developing and adult rats. Using a within-litter design, infant male and female rats were exposed to an adverse or nurturing caregiving environment outside their homecage for 30 minutes per day during the first postnatal week. Additional littermates remained with their biological caregiver within the homecage during the manipulations. We observed that infant rats subjected to caregiver maltreatment emitted more audible and ultrasonic vocalizations than littermates subjected to nurturing care either within or outside of the homecage. While we found no maltreatment-induced changes in bdnf DNA methylation present in infancy, sex-specific alterations were present in the mPFC of adolescents and adults that had been exposed to maltreatment. Furthermore, while maltreated-females showed differences in reelin DNA methylation that were transient, males exposed to maltreatment and both males and females exposed to nurturing care outside the homecage showed differences in reelin methylation that emerged by adulthood. Our results demonstrate the ability of infant-caregiver interactions to epigenetically mark genes known to play a prominent role in cognition and psychiatric disorders within the mPFC. Furthermore, our data indicate the remarkable complexity of alterations that can occur, with both transient and later-emerging DNA methylation differences that could shape developmental trajectories and underlie gender differences in outcomes. |
Author | Roth, Tania L. Blaze, Jennifer Scheuing, Lisa |
Author_xml | – sequence: 1 givenname: Jennifer surname: Blaze fullname: Blaze, Jennifer – sequence: 2 givenname: Lisa surname: Scheuing fullname: Scheuing, Lisa – sequence: 3 givenname: Tania L. surname: Roth fullname: Roth, Tania L. email: troth@psych.udel.edu |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23751776$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/j.euroneuro.2012.10.008 10.1016/j.bbagen.2009.06.009 10.1523/JNEUROSCI.5372-11.2012 10.3389/fpsyt.2011.00021 10.1038/npp.2012.112 10.1124/pr.111.005108 10.1016/j.biopsych.2008.11.028 10.1016/S0079-6123(07)67012-5 10.1016/j.biopsych.2012.01.034 10.1002/dev.20200 10.1159/000335524 10.1016/S0149-7634(05)80031-4 10.1371/journal.pone.0023881 10.1016/j.psyneuen.2009.05.014 10.1016/j.jpsychires.2011.01.013 10.1177/1524838009339758 10.1006/meth.2001.1262 10.1073/pnas.0507526103 10.1002/jnr.21139 10.1016/j.jaac.2010.06.001 10.1038/nn.2560 10.1016/j.neuroscience.2009.12.045 10.1523/JNEUROSCI.0859-10.2010 10.1016/j.neuropharm.2012.04.013 10.1073/pnas.1204599109 10.1017/S0954579411000460 10.1038/nn1276 10.1016/j.biopsych.2009.12.019 10.1016/S0006-3223(01)01157-X 10.3389/fpsyt.2011.00016 10.1038/nn.2270 10.1016/j.nlm.2012.03.007 10.1016/j.neuint.2011.01.020 10.1523/JNEUROSCI.1039-10.2010 10.1002/(SICI)1098-2302(199705)30:4<301::AID-DEV4>3.0.CO;2-S 10.1523/JNEUROSCI.1436-10.2010 10.1523/JNEUROSCI.1470-12.2012 10.1016/0306-4530(95)00042-9 10.4161/epi.6.7.16517 10.1038/nrn1113 10.1159/000336732 10.1523/JNEUROSCI.1786-08.2008 10.1101/lm.500907 10.1146/annurev.clinpsy.1.102803.144029 10.1037/0735-7044.122.2.310 10.1523/JNEUROSCI.1784-10.2010 10.1016/j.biopsych.2010.05.036 10.1002/hipo.20907 10.1523/JNEUROSCI.3331-09.2009 10.1002/ajmg.b.31212 10.1002/em.20357 10.1159/000330034 10.1038/nn.2436 10.1210/en.2005-1119 10.1111/j.1601-183X.2012.00805.x 10.1038/npp.2012.125 10.1016/j.bbr.2010.10.018 10.1016/S0006-3223(02)01459-2 10.1016/j.biopsych.2005.01.032 10.1159/000325264 10.1016/j.ajhg.2011.12.020 10.1016/j.neuroscience.2008.04.019 |
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Copyright | 2013 S. Karger AG, Basel Copyright © 2013 S. Karger AG, Basel. Copyright (c) 2013 S. Karger AG, Basel |
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Keywords | Early-life stress reelin gene Medial prefrontal cortex Maternal care Epigenetics DNA methylation bdnf gene |
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References | Maestripieri D, Lindell SG, Higley JD: Intergenerational transmission of maternal behavior in rhesus macaques and its underlying mechanisms. Dev Psychobiol 2007;49:165-171.1729978810.1002/dev.20200 Grayson DR, Guidotti A: The dynamics of DNA methylation in schizophrenia and related psychiatric disorders. Neuropsychopharmacology 2013;38:138-166.2294897510.1038/npp.2012.125 Matrisciano F, Tueting P, Dalal I, Kadriu B, Grayson DR, Davis JM, Nicoletti F, Guidotti A: Epigenetic modifications of GABAergic interneurons are associated with the schizophrenia-like phenotype induced by prenatal stress in mice. Neuropharmacology 2013;68:184-194.2256444010.1016/j.neuropharm.2012.04.013 McGowan PO, Sasaki A, D'Alessio AC, Dymov S, Labonte B, Szyf M, Turecki G, Meaney MJ: Epigenetic regulation of the glucocorticoid receptor in human brain associates with childhood abuse. Nat Neurosci 2009;12:342-348.1923445710.1038/nn.2270 Livak KJ, Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods 2001;25:402-408.1184660910.1006/meth.2001.1262 Roth TL, Sullivan RM: Memory of early maltreatment: neonatal behavioral and neural correlates of maternal maltreatment within the context of classical conditioning. Biol Psychiatry 2005;57:823-831.1582070210.1016/j.biopsych.2005.01.032 Lubin FD, Roth TL, Sweatt JD: Epigenetic regulation of bdnf gene transcription in the consolidation of fear memory. J Neurosci 2008;28:10576-10586.1892303410.1523/JNEUROSCI.1786-08.2008 Fuchikami M, Morinobu S, Segawa M, Okamoto Y, Yamawaki S, Ozaki N, Inoue T, Kusumi I, Koyama T, Tsuchiyama K, Terao T: DNA methylation profiles of the brain-derived neurotrophic factor (bdnf) gene as a potent diagnostic biomarker in major depression. PLoS One 2011;6:e23881.2191260910.1371/journal.pone.0023881 Howell BR, Sanchez MM: Understanding behavioral effects of early life stress using the reactive scope and allostatic load models. Dev Psychopathol 2011;23:1001-1016.2201807810.1017/S0954579411000460 Zhang T-Y, Hellstrom IC, Bagot RC, Wen X, Diorio J, Meaney MJ: Maternal care and DNA methylation of a glutamic acid decarboxylase 1 promoter in rat hippocampus. J Neurosci 2010;30:13130-13137.2088113110.1523/JNEUROSCI.1039-10.2010 Blumberg MS, Alberts JR: On the significance of similarities between ultrasonic vocalizations of infant and adult rats. Neurosci Biobehav Rev 1991;15:383-390.195660610.1016/S0149-7634(05)80031-4 Jessen HM, Auger AP: Sex differences in epigenetic mechanisms may underlie risk and resilience for mental health disorders. Epigenetics 2011;6:857-861.2161737010.4161/epi.6.7.16517 Mychasiuk R, Gibb R, Kolb B: Prenatal stress produces sexually dimorphic and regionally specific changes in gene expression in hippocampus and frontal cortex of developing rat offspring. Dev Neurosci 2011;33:531-538.2228669310.1159/000335524 Philip NS, Sweet LH, Tyrka AR, Price LH, Bloom RF, Carpenter LL: Decreased default network connectivity is associated with early life stress in medication-free healthy adults. Eur Neuropsychopharmacol 2013;23:24-32.2314115310.1016/j.euroneuro.2012.10.008 Nugent B, McCarthy M: Epigenetic underpinnings of developmental sex differences in the brain. Neuroendocrinology 2011;93:150-158.2141198210.1159/000325264 Uchida S, Hara K, Kobayashi A, Funato H, Hobara T, Otsuki K, Yamagata H, McEwen BS, Watanabe Y: Early life stress enhances behavioral vulnerability to stress through the activation of rest4-mediated gene transcription in the medial prefrontal cortex of rodents. J Neurosci 2010;30:15007-15018.2106830610.1523/JNEUROSCI.1436-10.2010 Tissir F, Goffinet AM: Reelin and brain development. Nat Rev Neurosci 2003;4:496-505.1277812110.1038/nrn1113 Murgatroyd C, Spengler D: Epigenetics of early child development. Front Psychiatry 2011;2:16.2164740210.3389/fpsyt.2011.00016 Smith AK, Conneely KN, Kilaru V, Mercer KB, Weiss TE, Bradley B, Tang Y, Gillespie CF, Cubells JF, Ressler KJ: Differential immune system DNA methylation and cytokine regulation in post-traumatic stress disorder. Am J Med Genet B Neuropsychiatr Genet 2011;156:700-708.2171407210.1002/ajmg.b.31212 Hofer MA: Multiple regulators of ultrasonic vocalization in the infant rat. Psychoneuroendocrinology 1996;21:203-217.877406310.1016/0306-4530(95)00042-9 Murgatroyd C, Patchev AV, Wu Y, Micale V, Bockmuhl Y, Fischer D, Holsboer F, Wotjak CT, Almeida OF, Spengler D: Dynamic DNA methylation programs persistent adverse effects of early-life stress. Nat Neurosci 2009;12:1559-1566.1989846810.1038/nn.2436 Gross CM, Flubacher A, Tinnes S, Heyer A, Scheller M, Herpfer I, Berger M, Frotscher M, Lieb K, Haas CA: Early life stress stimulates hippocampal reelin gene expression in a sex-specific manner: evidence for corticosterone-mediated action. Hippocampus 2012;22:409-420.2113652010.1002/hipo.20907 Wöhr M, Schwarting RKW: Maternal care, isolation-induced infant ultrasonic calling, and their relations to adult anxiety-related behavior in the rat. Behav Neurosci 2008;122:310-330.1841017110.1037/0735-7044.122.2.310 Sui L, Wang Y, Ju LH, Chen M: Epigenetic regulation of reelin and brain-derived neurotrophic factor genes in long-term potentiation in rat medial prefrontal cortex. Neurobiol Learn Mem 2012;97:425-440.2246974710.1016/j.nlm.2012.03.007 Portfors C: Types and functions of ultrasonic vocalizations in laboratory rats and mice. J Am Assoc Lab Anim Sci 2007;46:28-34.17203913 Raineki C, Moriceau S, Sullivan RM: Developing a neurobehavioral animal model of infant attachment to an abusive caregiver. Biol Psychiatry 2010;67:1137-1145.2016378710.1016/j.biopsych.2009.12.019 Roth TL, Zoladz PR, Sweatt JD, Diamond DM: Epigenetic modification of hippocampal bdnf DNA in adult rats in an animal model of post-traumatic stress disorder. J Psychiatr Res 2011;45:919-926.2130673610.1016/j.jpsychires.2011.01.013 Landers MS, Sullivan RM: The development and neurobiology of infant attachment and fear. Dev Neurosci 2012;34:101-114.2257192110.1159/000336732 Weaver ICG, Meaney MJ, Szyf M: Maternal care effects on the hippocampal transcriptome and anxiety-mediated behaviors in the offspring that are reversible in adulthood. Proc Natl Acad Sci USA 2006;103:3480-3485.1648437310.1073/pnas.0507526103 Bremner JD, Elzinga B, Schmahl C, Vermetten E: Structural and functional plasticity of the human brain in posttraumatic stress disorder. Prog Brain Res 2007;167:171-186.1803701410.1016/S0079-6123(07)67012-5 Neigh GN, Gillespie CF, Nemeroff CB: The neurobiological toll of child abuse and neglect. Trauma Violence Abuse 2009;10:389-410.1966113310.1177/1524838009339758 Moore LD, Le T, Fan G: DNA methylation and its basic function. Neuropsychopharmacology 2013;38:23-38.2278184110.1038/npp.2012.112 De Bellis MD, Keshavan MS, Shifflett H, Iyengar S, Beers SR, Hall J, Moritz G: Brain structures in pediatric maltreatment-related posttraumatic stress disorder: a sociodemographically matched study. Biol Psychiatry 2002;52:1066-1078.1246069010.1016/S0006-3223(02)01459-2 Heim C, Nemeroff CB: The role of childhood trauma in the neurobiology of mood and anxiety disorders: preclinical and clinical studies. Biol Psychiatry 2001;49:1023-1039.1143084410.1016/S0006-3223(01)01157-X Cicchetti D, Toth SL: Child maltreatment. Annu Rev Clin Psychol 2005;1:409-438.1771609410.1146/annurev.clinpsy.1.102803.144029 Miller CA, Gavin CF, White JA, Parrish RR, Honasoge A, Yancey CR, Rivera IM, Rubio MD, Rumbaugh G, Sweatt JD: Cortical DNA methylation maintains remote memory. Nat Neurosci 2010;13:664-666.2049555710.1038/nn.2560 Mychasiuk R, Schmold N, Ilnytskyy S, Kovalchuk O, Kolb B, Gibb R: Prenatal bystander stress alters brain, behavior, and the epigenome of developing rat offspring. Dev Neurosci 2011;33:159-169.2189394810.1159/000330034 Mizuno K, Dempster E, Mill J, Giese KP: Long-lasting regulation of hippocampal bdnf gene transcription after contextual fear conditioning. Genes Brain Behav 2012;11:651-659.2257469010.1111/j.1601-183X.2012.00805.x Hao Y, Huang W, Nielsen DA, Kosten TA: Litter gender composition and sex affect maternal behavior and DNA methylation levels of the oprm1 gene in rat offspring. Front Psychiatry 2011;2:21.2162983910.3389/fpsyt.2011.00021 Labonte B, Yerko V, Gross J, Mechawar N, Meaney MJ, Szyf M, Turecki G: Differential glucocorticoid receptor exon 1b, 1c, and 1h expression and methylation in suicide completers with a history of childhood abuse. Biol Psychiatry 2012;72:41-48.2244420110.1016/j.biopsych.2012.01.034 Ivy AS, Rex CS, Chen Y, Dubé C, Maras PM, Grigoriadis DE, Gall CM, Lynch G, Baram TZ: Hippocampal dysfunction and cognitive impairments provoked by chronic early-life stress involve excessive activation of CRH receptors. J Neurosci 2010;30:13005-13015.2088111810.1523/JNEUROSCI.1784-10.2010 Provençal N, Suderman MJ, Guillemin C, Massart R, Ruggiero A, Wang D, Bennett AJ, Pierre PJ, Friedman DP, Côté SM, Hallett M, Tremblay RE, Suomi SJ, Szyf M: The signature of maternal rearing in the methylome in rhesus macaque prefrontal cortex and T cells. J Neurosci 2012;32:15626-15642.2311519710.1523/JNEUROSCI.1470-12.2012 Martínez L, Jiménez V, García-Sepúlveda C, Ceballos F, Delgado JM, Niño-Moreno P, Doniz L, Saavedra-Alanís V, Castillo CG, Santoyo ME, González-Amaro R, Jiménez-Capdeville ME: Impact of early developmental arsenic exposure on promotor CPG-island methylation of genes involved in neuronal plasticity. Neurochem Int 2011;58:574-581.2130012510.1016/j.neuint.2011.01.020 Autry AE, Monteggia LM: Brain-derived neurotrophic factor and neuropsychiatric disorders. Pharmacol Rev 2012;64:238-258.2240761610.1124/pr.111.005108 Szyf M, McGowan P, Meaney MJ: The social environment and the epigenome. Environ Mol Mutagen 2008;49:46-60.1809533010.1002/em.20357 Roth TL, Lubin FD, Funk AJ, Sweatt JD: Lasting epigenetic influence of early-life adversity on the bdnf gene. Biol Psychiatry 2009;65:760-769.1915005410.1016/j.biopsych.2008.11.028 McCarthy MM, Arnold AP, Ball GF, Blaustein JD, De Vries GJ: Sex differences in the brain: the ref13 ref57 ref12 ref56 ref15 ref59 ref14 ref58 ref53 ref52 ref11 ref55 ref10 ref54 ref17 ref16 ref19 ref18 ref51 ref50 ref46 ref45 ref48 ref47 ref42 ref41 ref44 ref43 ref49 ref8 ref7 ref9 ref4 ref3 ref6 ref5 ref40 ref35 ref34 ref37 ref36 ref31 ref30 ref33 ref32 ref2 ref1 ref39 ref38 ref24 ref23 ref26 ref25 ref20 ref22 ref21 ref28 ref27 ref29 ref60 ref62 ref61 |
References_xml | – reference: Franklin TB, Russig H, Weiss IC, Gräff J, Linder N, Michalon A, Vizi S, Mansuy IM: Epigenetic transmission of the impact of early stress across generations. Biol Psychiatry 2010;68:408-415.2067387210.1016/j.biopsych.2010.05.036 – reference: Martínez L, Jiménez V, García-Sepúlveda C, Ceballos F, Delgado JM, Niño-Moreno P, Doniz L, Saavedra-Alanís V, Castillo CG, Santoyo ME, González-Amaro R, Jiménez-Capdeville ME: Impact of early developmental arsenic exposure on promotor CPG-island methylation of genes involved in neuronal plasticity. Neurochem Int 2011;58:574-581.2130012510.1016/j.neuint.2011.01.020 – reference: Autry AE, Monteggia LM: Brain-derived neurotrophic factor and neuropsychiatric disorders. Pharmacol Rev 2012;64:238-258.2240761610.1124/pr.111.005108 – reference: Bagot RC, Zhang T-Y, Wen X, Nguyen TTT, Nguyen H-B, Diorio J, Wong TP, Meaney MJ: Variations in postnatal maternal care and the epigenetic regulation of metabotropic glutamate receptor 1 expression and hippocampal function in the rat. Proc Nl Acad Sci USA 2012;109:17200-17207.2304567810.1073/pnas.1204599109 – reference: Mychasiuk R, Schmold N, Ilnytskyy S, Kovalchuk O, Kolb B, Gibb R: Prenatal bystander stress alters brain, behavior, and the epigenome of developing rat offspring. Dev Neurosci 2011;33:159-169.2189394810.1159/000330034 – reference: Hanson JL, Chung MK, Avants BB, Shirtcliff EA, Gee JC, Davidson RJ, Pollak SD: Early stress is associated with alterations in the orbitofrontal cortex: a tensor-based morphometry investigation of brain structure and behavioral risk. J Neurosci 2010;30:7466-7472.2051952110.1523/JNEUROSCI.0859-10.2010 – reference: Bluhm RL, Williamson PC, Osuch EA, Frewen PA, Stevens TK, Boksman K, Neufeld RWJ, Théberge J, Lanius RA: Alterations in default network connectivity in posttraumatic stress disorder related to early-life trauma. J Psychiatry Neurosci 2009;34:187-194.19448848 – reference: Calabrese F, Molteni R, Racagni G, Riva MA: Neuronal plasticity: a link between stress and mood disorders. Psychoneuroendocrinology 2009;34:S208-S216.1954142910.1016/j.psyneuen.2009.05.014 – reference: Moore CL, Wong L, Daum MC, Leclair OU: Mother-infant interactions in two strains of rats: implications for dissociating mechanism and function of a maternal pattern. Dev Psychobiol 1997;30:301-312.914250610.1002/(SICI)1098-2302(199705)30:4<301::AID-DEV4>3.0.CO;2-S – reference: Ivy AS, Rex CS, Chen Y, Dubé C, Maras PM, Grigoriadis DE, Gall CM, Lynch G, Baram TZ: Hippocampal dysfunction and cognitive impairments provoked by chronic early-life stress involve excessive activation of CRH receptors. J Neurosci 2010;30:13005-13015.2088111810.1523/JNEUROSCI.1784-10.2010 – reference: Weaver ICG, Meaney MJ, Szyf M: Maternal care effects on the hippocampal transcriptome and anxiety-mediated behaviors in the offspring that are reversible in adulthood. Proc Natl Acad Sci USA 2006;103:3480-3485.1648437310.1073/pnas.0507526103 – reference: Bagot RC, Meaney MJ: Epigenetics and the biological basis of gene × environment interactions. J Am Acad Child Adolesc Psychiatry 2010;49:752-771.2064331010.1016/j.jaac.2010.06.001 – reference: Weaver IC, Cervoni N, Champagne FA, D'Alessio AC, Sharma S, Seckl JR, Dymov S, Szyf M, Meaney MJ: Epigenetic programming by maternal behavior. Nat Neurosci 2004;7:847-854.1522092910.1038/nn1276 – reference: De Bellis MD, Keshavan MS, Shifflett H, Iyengar S, Beers SR, Hall J, Moritz G: Brain structures in pediatric maltreatment-related posttraumatic stress disorder: a sociodemographically matched study. Biol Psychiatry 2002;52:1066-1078.1246069010.1016/S0006-3223(02)01459-2 – reference: Mizuno K, Dempster E, Mill J, Giese KP: Long-lasting regulation of hippocampal bdnf gene transcription after contextual fear conditioning. Genes Brain Behav 2012;11:651-659.2257469010.1111/j.1601-183X.2012.00805.x – reference: Howell BR, Sanchez MM: Understanding behavioral effects of early life stress using the reactive scope and allostatic load models. Dev Psychopathol 2011;23:1001-1016.2201807810.1017/S0954579411000460 – reference: McCarthy MM, Auger AP, Bale TL, De Vries GJ, Dunn GA, Forger NG, Murray EK, Nugent BM, Schwarz JM, Wilson ME: The epigenetics of sex differences in the brain. J Neurosci 2009;29:12815-12823.1982879410.1523/JNEUROSCI.3331-09.2009 – reference: Grayson DR, Guidotti A: The dynamics of DNA methylation in schizophrenia and related psychiatric disorders. Neuropsychopharmacology 2013;38:138-166.2294897510.1038/npp.2012.125 – reference: Hao Y, Huang W, Nielsen DA, Kosten TA: Litter gender composition and sex affect maternal behavior and DNA methylation levels of the oprm1 gene in rat offspring. Front Psychiatry 2011;2:21.2162983910.3389/fpsyt.2011.00021 – reference: Bremner JD, Elzinga B, Schmahl C, Vermetten E: Structural and functional plasticity of the human brain in posttraumatic stress disorder. Prog Brain Res 2007;167:171-186.1803701410.1016/S0079-6123(07)67012-5 – reference: Philip NS, Sweet LH, Tyrka AR, Price LH, Bloom RF, Carpenter LL: Decreased default network connectivity is associated with early life stress in medication-free healthy adults. Eur Neuropsychopharmacol 2013;23:24-32.2314115310.1016/j.euroneuro.2012.10.008 – reference: Szyf M, McGowan P, Meaney MJ: The social environment and the epigenome. Environ Mol Mutagen 2008;49:46-60.1809533010.1002/em.20357 – reference: Murgatroyd C, Patchev AV, Wu Y, Micale V, Bockmuhl Y, Fischer D, Holsboer F, Wotjak CT, Almeida OF, Spengler D: Dynamic DNA methylation programs persistent adverse effects of early-life stress. Nat Neurosci 2009;12:1559-1566.1989846810.1038/nn.2436 – reference: Roth TL, Lubin FD, Funk AJ, Sweatt JD: Lasting epigenetic influence of early-life adversity on the bdnf gene. Biol Psychiatry 2009;65:760-769.1915005410.1016/j.biopsych.2008.11.028 – reference: Sui L, Wang Y, Ju LH, Chen M: Epigenetic regulation of reelin and brain-derived neurotrophic factor genes in long-term potentiation in rat medial prefrontal cortex. Neurobiol Learn Mem 2012;97:425-440.2246974710.1016/j.nlm.2012.03.007 – reference: Moore LD, Le T, Fan G: DNA methylation and its basic function. Neuropsychopharmacology 2013;38:23-38.2278184110.1038/npp.2012.112 – reference: Hofer MA: Multiple regulators of ultrasonic vocalization in the infant rat. Psychoneuroendocrinology 1996;21:203-217.877406310.1016/0306-4530(95)00042-9 – reference: Murgatroyd C, Spengler D: Epigenetics of early child development. Front Psychiatry 2011;2:16.2164740210.3389/fpsyt.2011.00016 – reference: Miller CA, Gavin CF, White JA, Parrish RR, Honasoge A, Yancey CR, Rivera IM, Rubio MD, Rumbaugh G, Sweatt JD: Cortical DNA methylation maintains remote memory. Nat Neurosci 2010;13:664-666.2049555710.1038/nn.2560 – reference: Numata S, Ye T, Hyde Thomas M, Guitart-Navarro X, Tao R, Wininger M, Colantuoni C, Weinberger DR, Kleinman JE, Lipska BK: DNA methylation signatures in development and aging of the human prefrontal cortex. Am J Hum Genet 2012;90:260-272.2230552910.1016/j.ajhg.2011.12.020 – reference: Provençal N, Suderman MJ, Guillemin C, Massart R, Ruggiero A, Wang D, Bennett AJ, Pierre PJ, Friedman DP, Côté SM, Hallett M, Tremblay RE, Suomi SJ, Szyf M: The signature of maternal rearing in the methylome in rhesus macaque prefrontal cortex and T cells. J Neurosci 2012;32:15626-15642.2311519710.1523/JNEUROSCI.1470-12.2012 – reference: Zhang T-Y, Hellstrom IC, Bagot RC, Wen X, Diorio J, Meaney MJ: Maternal care and DNA methylation of a glutamic acid decarboxylase 1 promoter in rat hippocampus. J Neurosci 2010;30:13130-13137.2088113110.1523/JNEUROSCI.1039-10.2010 – reference: Landers MS, Sullivan RM: The development and neurobiology of infant attachment and fear. Dev Neurosci 2012;34:101-114.2257192110.1159/000336732 – reference: Blumberg MS, Alberts JR: On the significance of similarities between ultrasonic vocalizations of infant and adult rats. Neurosci Biobehav Rev 1991;15:383-390.195660610.1016/S0149-7634(05)80031-4 – reference: Ivy AS, Brunson KL, Sandman C, Baram TZ: Dysfunctional nurturing behavior in rat dams with limited access to nesting material: a clinically relevant model for early-life stress. Neuroscience 2008;154:1132-1142.1850152110.1016/j.neuroscience.2008.04.019 – reference: Tissir F, Goffinet AM: Reelin and brain development. Nat Rev Neurosci 2003;4:496-505.1277812110.1038/nrn1113 – reference: Wöhr M, Schwarting RKW: Maternal care, isolation-induced infant ultrasonic calling, and their relations to adult anxiety-related behavior in the rat. Behav Neurosci 2008;122:310-330.1841017110.1037/0735-7044.122.2.310 – reference: Gross CM, Flubacher A, Tinnes S, Heyer A, Scheller M, Herpfer I, Berger M, Frotscher M, Lieb K, Haas CA: Early life stress stimulates hippocampal reelin gene expression in a sex-specific manner: evidence for corticosterone-mediated action. Hippocampus 2012;22:409-420.2113652010.1002/hipo.20907 – reference: Uchida S, Hara K, Kobayashi A, Funato H, Hobara T, Otsuki K, Yamagata H, McEwen BS, Watanabe Y: Early life stress enhances behavioral vulnerability to stress through the activation of rest4-mediated gene transcription in the medial prefrontal cortex of rodents. J Neurosci 2010;30:15007-15018.2106830610.1523/JNEUROSCI.1436-10.2010 – reference: McGowan PO, Sasaki A, D'Alessio AC, Dymov S, Labonte B, Szyf M, Turecki G, Meaney MJ: Epigenetic regulation of the glucocorticoid receptor in human brain associates with childhood abuse. Nat Neurosci 2009;12:342-348.1923445710.1038/nn.2270 – reference: Roth TL, Zoladz PR, Sweatt JD, Diamond DM: Epigenetic modification of hippocampal bdnf DNA in adult rats in an animal model of post-traumatic stress disorder. J Psychiatr Res 2011;45:919-926.2130673610.1016/j.jpsychires.2011.01.013 – reference: Raineki C, Moriceau S, Sullivan RM: Developing a neurobehavioral animal model of infant attachment to an abusive caregiver. Biol Psychiatry 2010;67:1137-1145.2016378710.1016/j.biopsych.2009.12.019 – reference: Lubin FD, Roth TL, Sweatt JD: Epigenetic regulation of bdnf gene transcription in the consolidation of fear memory. J Neurosci 2008;28:10576-10586.1892303410.1523/JNEUROSCI.1786-08.2008 – reference: Neigh GN, Gillespie CF, Nemeroff CB: The neurobiological toll of child abuse and neglect. Trauma Violence Abuse 2009;10:389-410.1966113310.1177/1524838009339758 – reference: Qin L, Tu W, Sun X, Zhang J, Chen Y, Zhao H: Retardation of neurobehavioral development and reelin down-regulation regulated by further DNA methylation in the hippocampus of the rat pups are associated with maternal deprivation. Behav Brain Res 2011;217:142-147.2097419210.1016/j.bbr.2010.10.018 – reference: Smith AK, Conneely KN, Kilaru V, Mercer KB, Weiss TE, Bradley B, Tang Y, Gillespie CF, Cubells JF, Ressler KJ: Differential immune system DNA methylation and cytokine regulation in post-traumatic stress disorder. Am J Med Genet B Neuropsychiatr Genet 2011;156:700-708.2171407210.1002/ajmg.b.31212 – reference: Fuchikami M, Morinobu S, Segawa M, Okamoto Y, Yamawaki S, Ozaki N, Inoue T, Kusumi I, Koyama T, Tsuchiyama K, Terao T: DNA methylation profiles of the brain-derived neurotrophic factor (bdnf) gene as a potent diagnostic biomarker in major depression. PLoS One 2011;6:e23881.2191260910.1371/journal.pone.0023881 – reference: Champagne FA, Weaver IC, Diorio J, Dymov S, Szyf M, Meaney MJ: Maternal care associated with methylation of the estrogen receptor-alpha1b promoter and estrogen receptor-alpha expression in the medial preoptic area of female offspring. Endocrinology 2006;147:2909-2915.1651383410.1210/en.2005-1119 – reference: Matrisciano F, Tueting P, Dalal I, Kadriu B, Grayson DR, Davis JM, Nicoletti F, Guidotti A: Epigenetic modifications of GABAergic interneurons are associated with the schizophrenia-like phenotype induced by prenatal stress in mice. Neuropharmacology 2013;68:184-194.2256444010.1016/j.neuropharm.2012.04.013 – reference: Heim C, Nemeroff CB: The role of childhood trauma in the neurobiology of mood and anxiety disorders: preclinical and clinical studies. Biol Psychiatry 2001;49:1023-1039.1143084410.1016/S0006-3223(01)01157-X – reference: Bredy TW, Wu H, Crego C, Zellhoefer J, Sun YE, Barad M: Histone modifications around individual bdnf gene promoters in prefrontal cortex are associated with extinction of conditioned fear. Learn Mem 2007;14:268-276.1752201510.1101/lm.500907 – reference: Nugent B, McCarthy M: Epigenetic underpinnings of developmental sex differences in the brain. Neuroendocrinology 2011;93:150-158.2141198210.1159/000325264 – reference: Livak KJ, Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods 2001;25:402-408.1184660910.1006/meth.2001.1262 – reference: Cassidy AW, Mulvany SK, Pangalos MN, Murphy KJ, Regan CM: Developmental emergence of reelin deficits in the prefrontal cortex of Wistar rats reared in social isolation. Neuroscience 2010;166:377-385.2003584110.1016/j.neuroscience.2009.12.045 – reference: Roth TL, Sullivan RM: Memory of early maltreatment: neonatal behavioral and neural correlates of maternal maltreatment within the context of classical conditioning. Biol Psychiatry 2005;57:823-831.1582070210.1016/j.biopsych.2005.01.032 – reference: Maestripieri D, Lindell SG, Higley JD: Intergenerational transmission of maternal behavior in rhesus macaques and its underlying mechanisms. Dev Psychobiol 2007;49:165-171.1729978810.1002/dev.20200 – reference: McCarthy MM, Arnold AP, Ball GF, Blaustein JD, De Vries GJ: Sex differences in the brain: the not so inconvenient truth. J Neurosci 2012;32:2241-2247.2239639810.1523/JNEUROSCI.5372-11.2012 – reference: Labonte B, Yerko V, Gross J, Mechawar N, Meaney MJ, Szyf M, Turecki G: Differential glucocorticoid receptor exon 1b, 1c, and 1h expression and methylation in suicide completers with a history of childhood abuse. Biol Psychiatry 2012;72:41-48.2244420110.1016/j.biopsych.2012.01.034 – reference: Aid T, Kazantseva A, Piirsoo M, Palm K, Timmusk T: Mouse and rat bdnf gene structure and expression revisited. J Neurosci Res 2007;85:525-535.1714975110.1002/jnr.21139 – reference: Portfors C: Types and functions of ultrasonic vocalizations in laboratory rats and mice. J Am Assoc Lab Anim Sci 2007;46:28-34.17203913 – reference: Cicchetti D, Toth SL: Child maltreatment. Annu Rev Clin Psychol 2005;1:409-438.1771609410.1146/annurev.clinpsy.1.102803.144029 – reference: Mychasiuk R, Gibb R, Kolb B: Prenatal stress produces sexually dimorphic and regionally specific changes in gene expression in hippocampus and frontal cortex of developing rat offspring. Dev Neurosci 2011;33:531-538.2228669310.1159/000335524 – reference: Jessen HM, Auger AP: Sex differences in epigenetic mechanisms may underlie risk and resilience for mental health disorders. Epigenetics 2011;6:857-861.2161737010.4161/epi.6.7.16517 – reference: Roth TL, Lubin FD, Sodhi M, Kleinman JE: Epigenetic mechanisms in schizophrenia. Biochim Biophys Acta 2009;1790:869-877.1955975510.1016/j.bbagen.2009.06.009 – ident: ref33 doi: 10.1016/j.euroneuro.2012.10.008 – ident: ref37 doi: 10.1016/j.bbagen.2009.06.009 – ident: ref55 doi: 10.1523/JNEUROSCI.5372-11.2012 – ident: ref57 doi: 10.3389/fpsyt.2011.00021 – ident: ref14 doi: 10.1038/npp.2012.112 – ident: ref35 doi: 10.1124/pr.111.005108 – ident: ref11 doi: 10.1016/j.biopsych.2008.11.028 – ident: ref2 doi: 10.1016/S0079-6123(07)67012-5 – ident: ref17 doi: 10.1016/j.biopsych.2012.01.034 – ident: ref9 doi: 10.1002/dev.20200 – ident: ref27 doi: 10.1159/000335524 – ident: ref50 doi: 10.1016/S0149-7634(05)80031-4 – ident: ref51 doi: 10.1371/journal.pone.0023881 – ident: ref34 doi: 10.1016/j.psyneuen.2009.05.014 – ident: ref46 doi: 10.1016/j.jpsychires.2011.01.013 – ident: ref4 doi: 10.1177/1524838009339758 – ident: ref44 doi: 10.1006/meth.2001.1262 – ident: ref19 doi: 10.1073/pnas.0507526103 – ident: ref45 doi: 10.1002/jnr.21139 – ident: ref12 doi: 10.1016/j.jaac.2010.06.001 – ident: ref24 doi: 10.1038/nn.2560 – ident: ref60 doi: 10.1016/j.neuroscience.2009.12.045 – ident: ref31 doi: 10.1523/JNEUROSCI.0859-10.2010 – ident: ref61 doi: 10.1016/j.neuropharm.2012.04.013 – ident: ref20 doi: 10.1073/pnas.1204599109 – ident: ref6 doi: 10.1017/S0954579411000460 – ident: ref15 doi: 10.1038/nn1276 – ident: ref42 doi: 10.1016/j.biopsych.2009.12.019 – ident: ref3 doi: 10.1016/S0006-3223(01)01157-X – ident: ref13 doi: 10.3389/fpsyt.2011.00016 – ident: ref16 doi: 10.1038/nn.2270 – ident: ref25 doi: 10.1016/j.nlm.2012.03.007 – ident: ref39 doi: 10.1016/j.neuint.2011.01.020 – ident: ref21 doi: 10.1523/JNEUROSCI.1039-10.2010 – ident: ref58 doi: 10.1002/(SICI)1098-2302(199705)30:4<301::AID-DEV4>3.0.CO;2-S – ident: ref29 doi: 10.1523/JNEUROSCI.1436-10.2010 – ident: ref26 doi: 10.1523/JNEUROSCI.1470-12.2012 – ident: ref49 doi: 10.1016/0306-4530(95)00042-9 – ident: ref53 doi: 10.4161/epi.6.7.16517 – ident: ref38 doi: 10.1038/nrn1113 – ident: ref8 doi: 10.1159/000336732 – ident: ref43 doi: 10.1523/JNEUROSCI.1786-08.2008 – ident: ref23 doi: 10.1101/lm.500907 – ident: ref1 doi: 10.1146/annurev.clinpsy.1.102803.144029 – ident: ref48 doi: 10.1037/0735-7044.122.2.310 – ident: ref7 doi: 10.1523/JNEUROSCI.1784-10.2010 – ident: ref10 doi: 10.1016/j.biopsych.2010.05.036 – ident: ref59 doi: 10.1002/hipo.20907 – ident: ref56 doi: 10.1523/JNEUROSCI.3331-09.2009 – ident: ref52 doi: 10.1002/ajmg.b.31212 – ident: ref5 doi: 10.1002/em.20357 – ident: ref28 doi: 10.1159/000330034 – ident: ref22 doi: 10.1038/nn.2436 – ident: ref18 doi: 10.1210/en.2005-1119 – ident: ref47 doi: 10.1111/j.1601-183X.2012.00805.x – ident: ref36 doi: 10.1038/npp.2012.125 – ident: ref32 doi: 10.1016/j.bbr.2010.10.018 – ident: ref30 doi: 10.1016/S0006-3223(02)01459-2 – ident: ref41 doi: 10.1016/j.biopsych.2005.01.032 – ident: ref54 doi: 10.1159/000325264 – ident: ref62 doi: 10.1016/j.ajhg.2011.12.020 – ident: ref40 doi: 10.1016/j.neuroscience.2008.04.019 |
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SubjectTerms | Animals Animals, Newborn Behavior, Animal - physiology Brain-Derived Neurotrophic Factor - biosynthesis Brain-Derived Neurotrophic Factor - genetics Cell Adhesion Molecules, Neuronal - biosynthesis Cell Adhesion Molecules, Neuronal - genetics Child Child Abuse DNA Methylation - genetics Epigenesis, Genetic - physiology Extracellular Matrix Proteins - biosynthesis Extracellular Matrix Proteins - genetics Female Gene Expression Humans Male Maternal Behavior Nerve Tissue Proteins - biosynthesis Nerve Tissue Proteins - genetics Neuronal Plasticity - genetics Neuronal Plasticity - physiology Original Paper Prefrontal Cortex - growth & development Prefrontal Cortex - metabolism Pregnancy Rats Rats, Long-Evans Reelin Protein Serine Endopeptidases - biosynthesis Serine Endopeptidases - genetics Sex Characteristics |
Title | Differential Methylation of Genes in the Medial Prefrontal Cortex of Developing and Adult Rats Following Exposure to Maltreatment or Nurturing Care During Infancy |
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