Interactive effects of early life adversity and adolescent basolateral amygdala activity on corticolimbic connectivity and behavior

Corticolimbic development is shaped by the environment and relies on coordinated neuronal activity. Prior work revealed that early life adversity (ELA) leads to hyperinnervation of basolateral amygdala (BLA) projections to the prefrontal cortex (PFC) beginning in early adolescence. Both ELA and cort...

Full description

Saved in:
Bibliographic Details
Main Authors: Caitlyn R. Cody, Emilce Artur de la Villarmois, Anabel M.M. Miguelez Fernández, Janelle P. Lardizabal, Kuei Y. Tseng, Heather C. Brenhouse
Format: Article
Language:English
Published: Elsevier 2025-09-01
Series:Neurobiology of Stress
Online Access:http://www.sciencedirect.com/science/article/pii/S2352289525000475
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849222580240646144
author Caitlyn R. Cody
Emilce Artur de la Villarmois
Anabel M.M. Miguelez Fernández
Janelle P. Lardizabal
Kuei Y. Tseng
Heather C. Brenhouse
author_facet Caitlyn R. Cody
Emilce Artur de la Villarmois
Anabel M.M. Miguelez Fernández
Janelle P. Lardizabal
Kuei Y. Tseng
Heather C. Brenhouse
author_sort Caitlyn R. Cody
collection DOAJ
description Corticolimbic development is shaped by the environment and relies on coordinated neuronal activity. Prior work revealed that early life adversity (ELA) leads to hyperinnervation of basolateral amygdala (BLA) projections to the prefrontal cortex (PFC) beginning in early adolescence. Both ELA and corticolimbic hyperconnectivity are associated with anxiety-like behavior, however the underlying developmental processes driving these effects are largely unknown. Here we investigated interactive impacts of rearing environment and neuronal activity on behavior and corticolimbic connectivity in rats. We first found that BLA-PFC hyperinnervation was associated with enhanced BLA-evoked PFC local field potentials in adolescents exposed to maternal separation (MS) ELA. Since ELA reportedly increases activity in the early-developing BLA, we further examined whether reducing BLA activity during adolescence influences behavior or enduring PFC innervation. During early adolescence, MS animals displayed heightened exploratory behaviors in an open field. Differences between rearing groups were not present during acute inhibition of glutamatergic BLA neurons, as BLA inhibition resembled the effects of MS on adolescent exploratory behaviors. To examine longer-lasting impacts of adolescent BLA activity on PFC innervation, BLA-originating axonal boutons were quantified in the PFC during emerging adulthood after adolescent BLA inhibition. We expanded previous findings to show that MS causes enduring BLA-PFC hyperinnervation. Surprisingly, adolescent BLA inhibition itself increased BLA-PFC innervation in control animals, suggesting that hyperpolarization of output neurons during early adolescence may contribute to aberrant development of efferent projections. Taken together, our results indicate that ELA yields increased BLA-PFC innervation in adulthood that may involve enhanced inhibitory signaling within developing BLA circuitry.
format Article
id doaj-art-a7ed35d039324588b8ee729aae974b2b
institution Kabale University
issn 2352-2895
language English
publishDate 2025-09-01
publisher Elsevier
record_format Article
series Neurobiology of Stress
spelling doaj-art-a7ed35d039324588b8ee729aae974b2b2025-08-26T04:14:23ZengElsevierNeurobiology of Stress2352-28952025-09-013810075310.1016/j.ynstr.2025.100753Interactive effects of early life adversity and adolescent basolateral amygdala activity on corticolimbic connectivity and behaviorCaitlyn R. Cody0Emilce Artur de la Villarmois1Anabel M.M. Miguelez Fernández2Janelle P. Lardizabal3Kuei Y. Tseng4Heather C. Brenhouse5Department of Psychology, Northeastern University, Boston, MA, 02115, USADepartment of Anatomy and Cell Biology, University of Illinois, Chicago, IL, 60612, USADepartment of Anatomy and Cell Biology, University of Illinois, Chicago, IL, 60612, USADepartment of Psychology, Northeastern University, Boston, MA, 02115, USADepartment of Anatomy and Cell Biology, University of Illinois, Chicago, IL, 60612, USADepartment of Psychology, Northeastern University, Boston, MA, 02115, USA; Corresponding author. 360 Huntington Ave 125 Nightingale Hall, Boston, MA, 02115, USA.Corticolimbic development is shaped by the environment and relies on coordinated neuronal activity. Prior work revealed that early life adversity (ELA) leads to hyperinnervation of basolateral amygdala (BLA) projections to the prefrontal cortex (PFC) beginning in early adolescence. Both ELA and corticolimbic hyperconnectivity are associated with anxiety-like behavior, however the underlying developmental processes driving these effects are largely unknown. Here we investigated interactive impacts of rearing environment and neuronal activity on behavior and corticolimbic connectivity in rats. We first found that BLA-PFC hyperinnervation was associated with enhanced BLA-evoked PFC local field potentials in adolescents exposed to maternal separation (MS) ELA. Since ELA reportedly increases activity in the early-developing BLA, we further examined whether reducing BLA activity during adolescence influences behavior or enduring PFC innervation. During early adolescence, MS animals displayed heightened exploratory behaviors in an open field. Differences between rearing groups were not present during acute inhibition of glutamatergic BLA neurons, as BLA inhibition resembled the effects of MS on adolescent exploratory behaviors. To examine longer-lasting impacts of adolescent BLA activity on PFC innervation, BLA-originating axonal boutons were quantified in the PFC during emerging adulthood after adolescent BLA inhibition. We expanded previous findings to show that MS causes enduring BLA-PFC hyperinnervation. Surprisingly, adolescent BLA inhibition itself increased BLA-PFC innervation in control animals, suggesting that hyperpolarization of output neurons during early adolescence may contribute to aberrant development of efferent projections. Taken together, our results indicate that ELA yields increased BLA-PFC innervation in adulthood that may involve enhanced inhibitory signaling within developing BLA circuitry.http://www.sciencedirect.com/science/article/pii/S2352289525000475
spellingShingle Caitlyn R. Cody
Emilce Artur de la Villarmois
Anabel M.M. Miguelez Fernández
Janelle P. Lardizabal
Kuei Y. Tseng
Heather C. Brenhouse
Interactive effects of early life adversity and adolescent basolateral amygdala activity on corticolimbic connectivity and behavior
Neurobiology of Stress
title Interactive effects of early life adversity and adolescent basolateral amygdala activity on corticolimbic connectivity and behavior
title_full Interactive effects of early life adversity and adolescent basolateral amygdala activity on corticolimbic connectivity and behavior
title_fullStr Interactive effects of early life adversity and adolescent basolateral amygdala activity on corticolimbic connectivity and behavior
title_full_unstemmed Interactive effects of early life adversity and adolescent basolateral amygdala activity on corticolimbic connectivity and behavior
title_short Interactive effects of early life adversity and adolescent basolateral amygdala activity on corticolimbic connectivity and behavior
title_sort interactive effects of early life adversity and adolescent basolateral amygdala activity on corticolimbic connectivity and behavior
url http://www.sciencedirect.com/science/article/pii/S2352289525000475
work_keys_str_mv AT caitlynrcody interactiveeffectsofearlylifeadversityandadolescentbasolateralamygdalaactivityoncorticolimbicconnectivityandbehavior
AT emilcearturdelavillarmois interactiveeffectsofearlylifeadversityandadolescentbasolateralamygdalaactivityoncorticolimbicconnectivityandbehavior
AT anabelmmmiguelezfernandez interactiveeffectsofearlylifeadversityandadolescentbasolateralamygdalaactivityoncorticolimbicconnectivityandbehavior
AT janelleplardizabal interactiveeffectsofearlylifeadversityandadolescentbasolateralamygdalaactivityoncorticolimbicconnectivityandbehavior
AT kueiytseng interactiveeffectsofearlylifeadversityandadolescentbasolateralamygdalaactivityoncorticolimbicconnectivityandbehavior
AT heathercbrenhouse interactiveeffectsofearlylifeadversityandadolescentbasolateralamygdalaactivityoncorticolimbicconnectivityandbehavior