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...

Full description

Saved in:
Bibliographic Details
Published inDevelopmental neuroscience Vol. 35; no. 4; pp. 306 - 316
Main Authors Blaze, Jennifer, Scheuing, Lisa, Roth, Tania L.
Format Journal Article
LanguageEnglish
Published Basel, Switzerland S. Karger AG 01.01.2013
Subjects
Online AccessGet full text
ISSN0378-5866
1421-9859
1421-9859
DOI10.1159/000350716

Cover

Loading…
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.
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
BookMark eNqFkk1vEzEQhi1URNPAgTtClrjQQ6g_1mv7UqlK2lKpBYTgvHLW3sTFsYPtLc3f6S_FS0IEFRInj_Q-M_N6Zo7AgQ_eAPASo3cYM3mCEKIMcVw_ASNcETyRgskDMEKUiwkTdX0IjlK6RQgTSfkzcEgoZ5jzegQeZrbrTDQ-W-XgjcnLjVPZBg9DBy-NNwlaD_PSFE0PyKdouhh8LuE0xGzuB3Bm7owLa-sXUHkNz3TvMvyscoIXwbnwYxDO79ch9dHAHOCNcjkalVelLwwRfuhj7uNATVUhZtv4ynfKt5vn4GmnXDIvdu8YfL04_zJ9P7n-eHk1PbuetBXjeVJRLQSSmMqqa4lmXHJGEROqGoaj-bwjmkpSc6nJnBZYUkExJ5VkmlZ0TsfgdFt33c9XRrfFW1SuWUe7UnHTBGWbvxVvl80i3DVUVFyWFYzB212BGL73JuVmZVNrnFPehD41mNeCCcJKt_-iFZEEi5oM6JtH6G3ooy-TKBQllBDCcaFe_2l-7_r3pgtwvAXaGFIqS9wjGDXDFTX7KyrsySO2tfnXVZR_W_fPjFfbjG8qLkzc197JPwG_ZtGQ
CitedBy_id crossref_primary_10_1007_s00438_022_01935_w
crossref_primary_10_2478_afpuc_2019_0005
crossref_primary_10_1002_dev_22144
crossref_primary_10_1002_dev_21775
crossref_primary_10_1016_j_neuroscience_2015_07_022
crossref_primary_10_1002_dev_21218
crossref_primary_10_1016_j_bbr_2016_07_025
crossref_primary_10_1038_s41398_019_0601_8
crossref_primary_10_3389_fncel_2016_00089
crossref_primary_10_1017_S095457941600081X
crossref_primary_10_1007_s40572_017_0172_x
crossref_primary_10_1016_j_semcdb_2015_04_004
crossref_primary_10_3390_brainsci11050605
crossref_primary_10_1038_s41398_019_0651_y
crossref_primary_10_1016_j_ijdevneu_2017_03_007
crossref_primary_10_3389_fnbeh_2015_00079
crossref_primary_10_1016_j_yhbeh_2025_105720
crossref_primary_10_1017_neu_2021_18
crossref_primary_10_1080_10253890_2023_2201325
crossref_primary_10_1007_s42844_020_00015_5
crossref_primary_10_1002_dev_22231
crossref_primary_10_1038_s41398_022_02076_9
crossref_primary_10_1016_j_yfrne_2024_101162
crossref_primary_10_20900_jpbs_20190004
crossref_primary_10_31887_DCNS_2019_21_4_enestler
crossref_primary_10_1002_dev_22212
crossref_primary_10_1016_j_neubiorev_2023_105113
crossref_primary_10_3390_ijerph16214123
crossref_primary_10_1007_s12038_016_9648_3
crossref_primary_10_3389_fnhum_2020_594244
crossref_primary_10_3390_ijerph16214280
crossref_primary_10_1016_j_neurobiolaging_2016_07_006
crossref_primary_10_1038_tp_2017_171
crossref_primary_10_1371_journal_pone_0101437
crossref_primary_10_1038_s41598_019_46539_4
crossref_primary_10_1016_j_neuropharm_2022_109367
crossref_primary_10_1159_000442878
crossref_primary_10_1080_15622975_2017_1322714
crossref_primary_10_1016_j_cpr_2018_01_006
crossref_primary_10_1016_j_semcdb_2017_09_033
crossref_primary_10_1016_j_bpsgos_2024_100426
crossref_primary_10_1139_apnm_2020_0923
crossref_primary_10_1017_S0954579417000128
crossref_primary_10_1016_j_infbeh_2019_101381
crossref_primary_10_3390_bs6040028
crossref_primary_10_1097_HRP_0000000000000300
crossref_primary_10_1016_j_bbi_2017_07_001
crossref_primary_10_1002_dev_21796
crossref_primary_10_1038_tp_2016_276
crossref_primary_10_3389_fpsyt_2022_950455
crossref_primary_10_1002_dev_21834
crossref_primary_10_1016_j_bbr_2014_07_001
crossref_primary_10_1371_journal_pone_0138293
crossref_primary_10_3389_fnhum_2022_740195
crossref_primary_10_3389_fpsyt_2023_1108485
crossref_primary_10_1080_10253890_2017_1343296
crossref_primary_10_1016_j_ijdevneu_2017_08_002
crossref_primary_10_1002_phy2_96
crossref_primary_10_3109_10253890_2015_1071790
crossref_primary_10_1016_j_ntt_2017_12_009
crossref_primary_10_1016_j_ijdevneu_2013_10_001
crossref_primary_10_1016_j_jad_2014_09_042
crossref_primary_10_1093_eep_dvw007
crossref_primary_10_1093_nutrit_nuy007
crossref_primary_10_1002_dev_21547
crossref_primary_10_1016_j_bbr_2015_05_028
crossref_primary_10_1016_j_yfrne_2015_11_001
crossref_primary_10_3917_cpsy2_075_0023
crossref_primary_10_1016_j_ijdevneu_2015_05_002
crossref_primary_10_2217_epi_2016_0075
crossref_primary_10_1016_j_ctrv_2016_11_004
crossref_primary_10_1016_j_ijdevneu_2019_05_002
crossref_primary_10_1097_FBP_0000000000000419
crossref_primary_10_3389_fnbeh_2018_00126
crossref_primary_10_3389_fnbeh_2019_00197
crossref_primary_10_1186_s13148_017_0367_x
crossref_primary_10_1016_j_bbr_2019_112396
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
ContentType Journal Article
Copyright 2013 S. Karger AG, Basel
Copyright © 2013 S. Karger AG, Basel.
Copyright (c) 2013 S. Karger AG, Basel
Copyright_xml – notice: 2013 S. Karger AG, Basel
– notice: Copyright © 2013 S. Karger AG, Basel.
– notice: Copyright (c) 2013 S. Karger AG, Basel
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7QR
7TK
7U7
7X7
7XB
88E
88G
8AO
8FD
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
C1K
CCPQU
DWQXO
FR3
FYUFA
GHDGH
GNUQQ
K9.
M0S
M1P
M2M
P64
PHGZM
PHGZT
PJZUB
PKEHL
PPXIY
PQEST
PQQKQ
PQUKI
PRINS
PSYQQ
Q9U
RC3
7X8
5PM
DOI 10.1159/000350716
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
Chemoreception Abstracts
Neurosciences Abstracts
Toxicology Abstracts
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Psychology Database (Alumni)
ProQuest Pharma Collection
Technology Research Database
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
Environmental Sciences and Pollution Management
ProQuest One
ProQuest Central Korea
Engineering Research Database
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
ProQuest Health & Medical Complete (Alumni)
Health & Medical Collection (Alumni)
Medical Database
Psychology Database
Biotechnology and BioEngineering Abstracts
ProQuest Central Premium
ProQuest One Academic (New)
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
ProQuest One Psychology
ProQuest Central Basic
Genetics Abstracts
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
ProQuest One Psychology
ProQuest Central Student
Technology Research Database
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Pharma Collection
ProQuest Central China
Environmental Sciences and Pollution Management
ProQuest Central
ProQuest Health & Medical Research Collection
Genetics Abstracts
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
Health & Medical Research Collection
Chemoreception Abstracts
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest Central Basic
Toxicology Abstracts
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Psychology Journals (Alumni)
Neurosciences Abstracts
ProQuest Hospital Collection (Alumni)
Biotechnology and BioEngineering Abstracts
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest Psychology Journals
ProQuest One Academic UKI Edition
Engineering Research Database
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
MEDLINE
ProQuest One Psychology

Genetics Abstracts
CrossRef

Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1421-9859
EndPage 316
ExternalDocumentID PMC3847900
3069774101
23751776
10_1159_000350716
350716
Genre Research Support, Non-U.S. Gov't
Journal Article
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: NIGMS NIH HHS
  grantid: P20 GM103653
– fundername: NIGMS NIH HHS
  grantid: 1P20GM103653
– fundername: National Institute of General Medical Sciences : NIGMS
  grantid: P20 GM103653 || GM
GroupedDBID ---
.55
.GJ
0~5
0~B
29F
30W
325
34G
36B
39C
3O.
3V.
4.4
53G
5GY
5RE
7X7
88E
8AO
8FI
8FJ
8UI
AAYIC
ABIVO
ABJNI
ABPAZ
ABUWG
ACCCW
ACGFO
ACGFS
ACIWK
ACPRK
ACPSR
ADAGL
ADBBV
ADFRT
ADGES
ADOJD
AENEX
AEYAO
AFFNX
AFJJK
AFKRA
AFRAH
AHMBA
ALDHI
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AZPMC
AZQEC
BENPR
BPHCQ
BVXVI
CAG
CCPQU
COF
CS3
CYUIP
DU5
DWQXO
E0A
EBS
EJD
EMB
EMOBN
F5P
FB.
FYUFA
GNUQQ
HMCUK
HZ~
IY7
KUZGX
M1P
M2M
N9A
O1H
O9-
P2P
PQQKQ
PROAC
PSQYO
PSYQQ
RIG
RKO
RXVBD
SV3
TN5
UJ6
UKHRP
X7M
YYP
ZGI
ZXP
AAYXX
ABBTS
ABWCG
ACQXL
AFSIO
AHDLI
AHFRZ
CITATION
PHGZM
PHGZT
PJZUB
PPXIY
CGR
CUY
CVF
ECM
EIF
NPM
7QR
7TK
7U7
7XB
8FD
8FK
C1K
FR3
K9.
P64
PKEHL
PQEST
PQUKI
PRINS
Q9U
RC3
7X8
5PM
ID FETCH-LOGICAL-c457t-43d88091394fc2d579753058a40350d7bf2d392679d2b33d89383172495d343b3
IEDL.DBID 7X7
ISSN 0378-5866
1421-9859
IngestDate Thu Aug 21 18:30:23 EDT 2025
Mon Jul 21 10:20:06 EDT 2025
Tue Aug 05 10:56:55 EDT 2025
Fri Aug 15 23:01:28 EDT 2025
Mon Jul 21 06:02:38 EDT 2025
Thu Apr 24 22:57:10 EDT 2025
Tue Aug 05 12:00:29 EDT 2025
Thu Aug 29 12:04:24 EDT 2024
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords Early-life stress
reelin gene
Medial prefrontal cortex
Maternal care
Epigenetics
DNA methylation
bdnf gene
Language English
License Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
https://www.karger.com/Services/SiteLicenses
Copyright © 2013 S. Karger AG, Basel.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c457t-43d88091394fc2d579753058a40350d7bf2d392679d2b33d89383172495d343b3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
OpenAccessLink https://karger.com/dne/article-pdf/35/4/306/2628984/000350716.pdf
PMID 23751776
PQID 1432322271
PQPubID 34046
PageCount 11
ParticipantIDs crossref_primary_10_1159_000350716
pubmed_primary_23751776
pubmedcentral_primary_oai_pubmedcentral_nih_gov_3847900
proquest_journals_1432322271
proquest_miscellaneous_1768582534
karger_primary_350716
proquest_miscellaneous_1429218624
crossref_citationtrail_10_1159_000350716
PublicationCentury 2000
PublicationDate 2013-01-01
PublicationDateYYYYMMDD 2013-01-01
PublicationDate_xml – month: 01
  year: 2013
  text: 2013-01-01
  day: 01
PublicationDecade 2010
PublicationPlace Basel, Switzerland
PublicationPlace_xml – name: Basel, Switzerland
– name: Switzerland
– name: Basel
PublicationTitle Developmental neuroscience
PublicationTitleAlternate Dev Neurosci
PublicationYear 2013
Publisher S. Karger AG
Publisher_xml – name: S. Karger AG
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
SSID ssj0012937
Score 2.3494656
Snippet Quality of maternal care in infancy is an important contributing factor in the development of behavior and psychopathology. One way maternal care could affect...
SourceID pubmedcentral
proquest
pubmed
crossref
karger
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 306
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
URI https://karger.com/doi/10.1159/000350716
https://www.ncbi.nlm.nih.gov/pubmed/23751776
https://www.proquest.com/docview/1432322271
https://www.proquest.com/docview/1429218624
https://www.proquest.com/docview/1768582534
https://pubmed.ncbi.nlm.nih.gov/PMC3847900
Volume 35
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3fa9RAEF60FfFF_FH1tJZRfPAlNN3dZJInqb07qpCjFAv3FrLZhBaP5LzLYf8e_1Jnkr21ldK3kB3IktnZ-XZn5hshPmFqVFKhCUqZ6kDbOg6SEqPAlmmcIHmIIuba4WwWn17o7_No7i7c1i6tcrsn9hu1bUu-Iz8kvy45KoBHX5a_Au4axdFV10Ljodhl6jI-fOHcH7jYlfXl0gq5uiiOHbMQefDDIaSG3Ob8hj969JPTr1d3oc3_kyZveKHpM_HUwUc4HvT9XDyomhficeYC5C_Fn7FreEKGu4CsIjUMyW7Q1sAU02u4aoBAH2R9yQic0YyYw4AeTzjv9poFx76SCorGwjFzdMB50a1hSsum_c0Dk-tly7eL0LWQFQufsA7tCmabVdeXPwKXN8F4eP7W1LyV74mL6eTHyWng2jAEpY6wC7SyZORMH6rrUtoIuRY3jJJC8y-0aGppCWXFmFppFAmndOolXERHL6u0MuqV2GnapnojQJtaKUMY0ZShrgmZJbWpmHEedWgImYzE560y8tJxlHOrjEXen1WiNPd6G4mPXnQ5EHPcJbQ3aNSLbN_vbxWcO5td5_9W2Eh88MNkbRxCKZqq3bCMTLmLl9T3yCBz-stIkczrYc34z0uF0REiTQBvrSYvwGzft0eaq8ue9VsRjkjD8O39U38nnsi-YQdfEu2LnW61qd4TbOrMQW8bB2L362R2dv4X1EMXTg
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1fT9RAEN8gGvWF-AflAHU0mvjSUHa33fbBGMJxuRN6MQaSeyvdbhsJl_a86wX4On4AP6Mz_bOCIbzx1nQn7SYzu_PbnZnfMPZRhVoEmdJOykPpSJP7TpAqzzFp6AcKPUTiU-1wNPaHJ_LbxJussD9dLQylVXZ7Yr1RmzKlO_Id9OucogJq9-vsl0Ndoyi62rXQaMziMLu6wCPb4suoj_r9xPng4Hh_6LRdBZxUeqpypDBos8SGKfOUG09RaanrBYmkIJtROucGQYOvQsO1QOEQD3Ho5vEkYYQUWuB3H7CH6HhdSiFUE3vAI9dZl2cLRdVMvt8yGSFi2GlCeIraql_zf4_OKd17fhu6_T9J85rXGzxjay1chb3Gvp6zlax4wR5HbUD-Jfvdbxus4EYxhShDtTfJdVDmQJTWCzgrAEEmRHWJCnzHGRFnAj7uU57vJQn2beUWJIWBPeIEgR9JtYABmml5QQMHl7OSbjOhKiFKpjZBHso5jJfzqi63BCqngn7zPCpych3r7OReFPSKrRZlkW0wkDoXQiMm1akrc0SCQa4zYrhX0tWIhHrsc6eMOG050ak1xzSuz0ZeGFu99dgHKzpriEBuE1pvNGpFuvfbnYLjdo9YxP8susfe22Fc3RSySYqsXJIMD6lrGJd3yCjqIcA9gTKvG5uxv-dCebtK4QTUDWuyAsQufnOkOPtZs4wLxC2h627ePfV37MnwODqKj0bjwy32lNfNQuiCaputVvNl9gYhW6Xf1usE2Ol9L8y_f4ROyQ
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Differential+methylation+of+genes+in+the+medial+prefrontal+cortex+of+developing+and+adult+rats+following+exposure+to+maltreatment+or+nurturing+care+during+infancy&rft.jtitle=Developmental+neuroscience&rft.au=Blaze%2C+Jennifer&rft.au=Scheuing%2C+Lisa&rft.au=Roth%2C+Tania+L.&rft.date=2013-01-01&rft.issn=0378-5866&rft.eissn=1421-9859&rft.volume=35&rft.issue=4&rft_id=info:doi/10.1159%2F000350716&rft_id=info%3Apmid%2F23751776&rft.externalDocID=PMC3847900
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0378-5866&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0378-5866&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0378-5866&client=summon