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Early life stress and macaque amygdala hypertrophy: preliminary evidence for a role for the serotonin transporter gene

Background: Children exposed to early life stress (ELS) exhibit enlarged amygdala volume in comparison to controls. The primary goal of this study was to examine amygdala volumes in bonnet macaques subjected to maternal variable foraging demand (VFD) rearing, a well-established model of ELS. Prelimi...

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Autores principales: Coplan, Jeremy D., Fathy, Hassan M., Jackowski, Andrea P., Tang, Cheuk Y., Perera, Tarique D., Mathew, Sanjay J., Martinez, Jose, Abdallah, Chadi G., Dwork, Andrew J., Pantol, Gustavo, Carpenter, David, Gorman, Jack M., Nemeroff, Charles B., Owens, Michael J., Kaffman, Arie, Kaufman, Joan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186477/
https://www.ncbi.nlm.nih.gov/pubmed/25339875
http://dx.doi.org/10.3389/fnbeh.2014.00342
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author Coplan, Jeremy D.
Fathy, Hassan M.
Jackowski, Andrea P.
Tang, Cheuk Y.
Perera, Tarique D.
Mathew, Sanjay J.
Martinez, Jose
Abdallah, Chadi G.
Dwork, Andrew J.
Pantol, Gustavo
Carpenter, David
Gorman, Jack M.
Nemeroff, Charles B.
Owens, Michael J.
Kaffman, Arie
Kaufman, Joan
author_facet Coplan, Jeremy D.
Fathy, Hassan M.
Jackowski, Andrea P.
Tang, Cheuk Y.
Perera, Tarique D.
Mathew, Sanjay J.
Martinez, Jose
Abdallah, Chadi G.
Dwork, Andrew J.
Pantol, Gustavo
Carpenter, David
Gorman, Jack M.
Nemeroff, Charles B.
Owens, Michael J.
Kaffman, Arie
Kaufman, Joan
author_sort Coplan, Jeremy D.
collection PubMed
description Background: Children exposed to early life stress (ELS) exhibit enlarged amygdala volume in comparison to controls. The primary goal of this study was to examine amygdala volumes in bonnet macaques subjected to maternal variable foraging demand (VFD) rearing, a well-established model of ELS. Preliminary analyses examined the interaction of ELS and the serotonin transporter gene on amygdala volume. Secondary analyses were conducted to examine the association between amygdala volume and other stress-related variables previously found to distinguish VFD and non-VFD reared animals. Methods: Twelve VFD-reared and nine normally reared monkeys completed MRI scans on a 3T system (mean age = 5.2 years). Results: Left amygdala volume was larger in VFD vs. control macaques. Larger amygdala volume was associated with: “high” cerebrospinal fluid concentrations of corticotropin releasing-factor (CRF) determined when the animals were in adolescence (mean age = 2.7 years); reduced fractional anisotropy (FA) of the anterior limb of the internal capsule (ALIC) during young adulthood (mean age = 5.2 years) and timid anxiety-like responses to an intruder during full adulthood (mean age = 8.4 years). Right amygdala volume varied inversely with left hippocampal neurogenesis assessed in late adulthood (mean age = 8.7 years). Exploratory analyses also showed a gene-by-environment effect, with VFD-reared macaques with a single short allele of the serotonin transporter gene exhibiting larger amygdala volume compared to VFD-reared subjects with only the long allele and normally reared controls. Conclusion: These data suggest that the left amygdala exhibits hypertrophy after ELS, particularly in association with the serotonin transporter gene, and that amygdala volume variation occurs in concert with other key stress-related behavioral and neurobiological parameters observed across the lifecycle. Future research is required to understand the mechanisms underlying these diverse and persistent changes associated with ELS and amygdala volume.
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spelling pubmed-41864772014-10-22 Early life stress and macaque amygdala hypertrophy: preliminary evidence for a role for the serotonin transporter gene Coplan, Jeremy D. Fathy, Hassan M. Jackowski, Andrea P. Tang, Cheuk Y. Perera, Tarique D. Mathew, Sanjay J. Martinez, Jose Abdallah, Chadi G. Dwork, Andrew J. Pantol, Gustavo Carpenter, David Gorman, Jack M. Nemeroff, Charles B. Owens, Michael J. Kaffman, Arie Kaufman, Joan Front Behav Neurosci Neuroscience Background: Children exposed to early life stress (ELS) exhibit enlarged amygdala volume in comparison to controls. The primary goal of this study was to examine amygdala volumes in bonnet macaques subjected to maternal variable foraging demand (VFD) rearing, a well-established model of ELS. Preliminary analyses examined the interaction of ELS and the serotonin transporter gene on amygdala volume. Secondary analyses were conducted to examine the association between amygdala volume and other stress-related variables previously found to distinguish VFD and non-VFD reared animals. Methods: Twelve VFD-reared and nine normally reared monkeys completed MRI scans on a 3T system (mean age = 5.2 years). Results: Left amygdala volume was larger in VFD vs. control macaques. Larger amygdala volume was associated with: “high” cerebrospinal fluid concentrations of corticotropin releasing-factor (CRF) determined when the animals were in adolescence (mean age = 2.7 years); reduced fractional anisotropy (FA) of the anterior limb of the internal capsule (ALIC) during young adulthood (mean age = 5.2 years) and timid anxiety-like responses to an intruder during full adulthood (mean age = 8.4 years). Right amygdala volume varied inversely with left hippocampal neurogenesis assessed in late adulthood (mean age = 8.7 years). Exploratory analyses also showed a gene-by-environment effect, with VFD-reared macaques with a single short allele of the serotonin transporter gene exhibiting larger amygdala volume compared to VFD-reared subjects with only the long allele and normally reared controls. Conclusion: These data suggest that the left amygdala exhibits hypertrophy after ELS, particularly in association with the serotonin transporter gene, and that amygdala volume variation occurs in concert with other key stress-related behavioral and neurobiological parameters observed across the lifecycle. Future research is required to understand the mechanisms underlying these diverse and persistent changes associated with ELS and amygdala volume. Frontiers Media S.A. 2014-10-06 /pmc/articles/PMC4186477/ /pubmed/25339875 http://dx.doi.org/10.3389/fnbeh.2014.00342 Text en Copyright © 2014 Coplan, Fathy, Jackowski, Tang, Perera, Mathew, Martinez, Abdallah, Dwork, Pantol, Carpenter, Gorman, Nemeroff, Owens, Kaffman and Kaufman. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Coplan, Jeremy D.
Fathy, Hassan M.
Jackowski, Andrea P.
Tang, Cheuk Y.
Perera, Tarique D.
Mathew, Sanjay J.
Martinez, Jose
Abdallah, Chadi G.
Dwork, Andrew J.
Pantol, Gustavo
Carpenter, David
Gorman, Jack M.
Nemeroff, Charles B.
Owens, Michael J.
Kaffman, Arie
Kaufman, Joan
Early life stress and macaque amygdala hypertrophy: preliminary evidence for a role for the serotonin transporter gene
title Early life stress and macaque amygdala hypertrophy: preliminary evidence for a role for the serotonin transporter gene
title_full Early life stress and macaque amygdala hypertrophy: preliminary evidence for a role for the serotonin transporter gene
title_fullStr Early life stress and macaque amygdala hypertrophy: preliminary evidence for a role for the serotonin transporter gene
title_full_unstemmed Early life stress and macaque amygdala hypertrophy: preliminary evidence for a role for the serotonin transporter gene
title_short Early life stress and macaque amygdala hypertrophy: preliminary evidence for a role for the serotonin transporter gene
title_sort early life stress and macaque amygdala hypertrophy: preliminary evidence for a role for the serotonin transporter gene
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186477/
https://www.ncbi.nlm.nih.gov/pubmed/25339875
http://dx.doi.org/10.3389/fnbeh.2014.00342
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