Developmental outcomes of early adverse care on amygdala functional connectivity in nonhuman primates.
amygdala functional connectivity
childhood maltreatment
early life stress
prefrontal cortex
rhesus monkey
Journal
Development and psychopathology
ISSN: 1469-2198
Titre abrégé: Dev Psychopathol
Pays: United States
ID NLM: 8910645
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
entrez:
11
1
2021
pubmed:
12
1
2021
medline:
15
1
2021
Statut:
ppublish
Résumé
Despite the strong link between childhood maltreatment and psychopathology, the underlying neurodevelopmental mechanisms are poorly understood and difficult to disentangle from heritable and prenatal factors. This study used a translational macaque model of infant maltreatment in which the adverse experience occurs in the first months of life, during intense maturation of amygdala circuits important for stress and emotional regulation. Thus, we examined the developmental impact of maltreatment on amygdala functional connectivity (FC) longitudinally, from infancy through the juvenile period. Using resting state functional magnetic resonance imaging (MRI) we performed amygdala-prefrontal cortex (PFC) region-of-interest and exploratory whole-brain amygdala FC analyses. The latter showed (a) developmental increases in amygdala FC with many regions, likely supporting increased processing of socioemotional-relevant stimuli with age; and (b) maltreatment effects on amygdala coupling with arousal and stress brain regions (locus coeruleus, laterodorsal tegmental area) that emerged with age. Maltreated juveniles showed weaker FC than controls, which was negatively associated with infant hair cortisol concentrations. Findings from the region-of-interest analysis also showed weaker amygdala FC with PFC regions in maltreated animals than controls since infancy, whereas bilateral amygdala FC was stronger in maltreated animals. These effects on amygdala FC development may underlie the poor behavioral outcomes associated with this adverse experience.
Identifiants
pubmed: 33427167
doi: 10.1017/S0954579420001133
pii: S0954579420001133
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
1579-1596Subventions
Organisme : NLM NIH HHS
ID : T15 LM007088
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000128
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA038588
Pays : United States
Organisme : NIH HHS
ID : P51 OD011132
Pays : United States
Organisme : NIMH NIH HHS
ID : F31 MH086203
Pays : United States
Organisme : NIMH NIH HHS
ID : P50 MH078105
Pays : United States
Organisme : NICHD NIH HHS
ID : R21 HD055255
Pays : United States