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Altered corticolimbic connectivity reveals sex-specific adolescent outcomes in a rat model of early life adversity

Exposure to early-life adversity (ELA) increases the risk for psychopathologies associated with amygdala-prefrontal cortex (PFC) circuits. While sex differences in vulnerability have been identified with a clear need for individualized intervention strategies, the neurobiological substrates of ELA-a...

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Autores principales: Honeycutt, Jennifer A, Demaestri, Camila, Peterzell, Shayna, Silveri, Marisa M, Cai, Xuezhu, Kulkarni, Praveen, Cunningham, Miles G, Ferris, Craig F, Brenhouse, Heather C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010412/
https://www.ncbi.nlm.nih.gov/pubmed/31958061
http://dx.doi.org/10.7554/eLife.52651
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author Honeycutt, Jennifer A
Demaestri, Camila
Peterzell, Shayna
Silveri, Marisa M
Cai, Xuezhu
Kulkarni, Praveen
Cunningham, Miles G
Ferris, Craig F
Brenhouse, Heather C
author_facet Honeycutt, Jennifer A
Demaestri, Camila
Peterzell, Shayna
Silveri, Marisa M
Cai, Xuezhu
Kulkarni, Praveen
Cunningham, Miles G
Ferris, Craig F
Brenhouse, Heather C
author_sort Honeycutt, Jennifer A
collection PubMed
description Exposure to early-life adversity (ELA) increases the risk for psychopathologies associated with amygdala-prefrontal cortex (PFC) circuits. While sex differences in vulnerability have been identified with a clear need for individualized intervention strategies, the neurobiological substrates of ELA-attributable differences remain unknown due to a paucity of translational investigations taking both development and sex into account. Male and female rats exposed to maternal separation ELA were analyzed with anterograde tracing from basolateral amygdala (BLA) to PFC to identify sex-specific innervation trajectories through juvenility (PD28) and adolescence (PD38;PD48). Resting-state functional connectivity (rsFC) was assessed longitudinally (PD28;PD48) in a separate cohort. All measures were related to anxiety-like behavior. ELA-exposed rats showed precocial maturation of BLA-PFC innervation, with females affected earlier than males. ELA also disrupted maturation of female rsFC, with enduring relationships between rsFC and anxiety-like behavior. This study is the first providing both anatomical and functional evidence for sex- and experience-dependent corticolimbic development.
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spelling pubmed-70104122020-02-12 Altered corticolimbic connectivity reveals sex-specific adolescent outcomes in a rat model of early life adversity Honeycutt, Jennifer A Demaestri, Camila Peterzell, Shayna Silveri, Marisa M Cai, Xuezhu Kulkarni, Praveen Cunningham, Miles G Ferris, Craig F Brenhouse, Heather C eLife Developmental Biology Exposure to early-life adversity (ELA) increases the risk for psychopathologies associated with amygdala-prefrontal cortex (PFC) circuits. While sex differences in vulnerability have been identified with a clear need for individualized intervention strategies, the neurobiological substrates of ELA-attributable differences remain unknown due to a paucity of translational investigations taking both development and sex into account. Male and female rats exposed to maternal separation ELA were analyzed with anterograde tracing from basolateral amygdala (BLA) to PFC to identify sex-specific innervation trajectories through juvenility (PD28) and adolescence (PD38;PD48). Resting-state functional connectivity (rsFC) was assessed longitudinally (PD28;PD48) in a separate cohort. All measures were related to anxiety-like behavior. ELA-exposed rats showed precocial maturation of BLA-PFC innervation, with females affected earlier than males. ELA also disrupted maturation of female rsFC, with enduring relationships between rsFC and anxiety-like behavior. This study is the first providing both anatomical and functional evidence for sex- and experience-dependent corticolimbic development. eLife Sciences Publications, Ltd 2020-01-20 /pmc/articles/PMC7010412/ /pubmed/31958061 http://dx.doi.org/10.7554/eLife.52651 Text en © 2020, Honeycutt et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Honeycutt, Jennifer A
Demaestri, Camila
Peterzell, Shayna
Silveri, Marisa M
Cai, Xuezhu
Kulkarni, Praveen
Cunningham, Miles G
Ferris, Craig F
Brenhouse, Heather C
Altered corticolimbic connectivity reveals sex-specific adolescent outcomes in a rat model of early life adversity
title Altered corticolimbic connectivity reveals sex-specific adolescent outcomes in a rat model of early life adversity
title_full Altered corticolimbic connectivity reveals sex-specific adolescent outcomes in a rat model of early life adversity
title_fullStr Altered corticolimbic connectivity reveals sex-specific adolescent outcomes in a rat model of early life adversity
title_full_unstemmed Altered corticolimbic connectivity reveals sex-specific adolescent outcomes in a rat model of early life adversity
title_short Altered corticolimbic connectivity reveals sex-specific adolescent outcomes in a rat model of early life adversity
title_sort altered corticolimbic connectivity reveals sex-specific adolescent outcomes in a rat model of early life adversity
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010412/
https://www.ncbi.nlm.nih.gov/pubmed/31958061
http://dx.doi.org/10.7554/eLife.52651
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