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Early Attachment Disruption, Inflammation, and Vulnerability for Depression in Rodent and Primate Models

Early experiments in nonhuman primates established the relation between disruption of filial attachment and depressive-like outcomes. Subsequent studies in rats and mice have been instrumental in linking depressive-like outcomes to disturbances in maternal behavior. Another aspect of attachment disr...

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Autores principales: Hennessy, Michael B., Schiml, Patricia A., Berberich, Katelyn, Beasley, Nicole L., Deak, Terrence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330302/
https://www.ncbi.nlm.nih.gov/pubmed/30666192
http://dx.doi.org/10.3389/fnbeh.2018.00314
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author Hennessy, Michael B.
Schiml, Patricia A.
Berberich, Katelyn
Beasley, Nicole L.
Deak, Terrence
author_facet Hennessy, Michael B.
Schiml, Patricia A.
Berberich, Katelyn
Beasley, Nicole L.
Deak, Terrence
author_sort Hennessy, Michael B.
collection PubMed
description Early experiments in nonhuman primates established the relation between disruption of filial attachment and depressive-like outcomes. Subsequent studies in rats and mice have been instrumental in linking depressive-like outcomes to disturbances in maternal behavior. Another aspect of attachment disruption, absence of the attachment object per se, may be studied more effectively in a different laboratory rodent—the guinea pig. Here, we discuss the rationale for using guinea pigs for this work. We then review guinea pig studies providing evidence for inflammatory mechanisms mediating both depressive-like behavior during separation as well as sensitization of stress responsiveness such as is thought to lead to increased vulnerability to depression at later ages. Finally, we discuss recent complementary work in adult monkeys that suggests cross-species generalizability of broad principles derived from the guinea pig experiments. Overall, the findings provide experimental support for human research implicating inflammatory mechanisms in the development of increased stress responsiveness and vulnerability to depression following attachment disruption and other forms of early-life stress. Specifically, the findings suggest inflammatory mechanisms may set in motion a cascade of underlying processes that mediate later increased stress responsiveness and, therefore, depression susceptibility.
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spelling pubmed-63303022019-01-21 Early Attachment Disruption, Inflammation, and Vulnerability for Depression in Rodent and Primate Models Hennessy, Michael B. Schiml, Patricia A. Berberich, Katelyn Beasley, Nicole L. Deak, Terrence Front Behav Neurosci Neuroscience Early experiments in nonhuman primates established the relation between disruption of filial attachment and depressive-like outcomes. Subsequent studies in rats and mice have been instrumental in linking depressive-like outcomes to disturbances in maternal behavior. Another aspect of attachment disruption, absence of the attachment object per se, may be studied more effectively in a different laboratory rodent—the guinea pig. Here, we discuss the rationale for using guinea pigs for this work. We then review guinea pig studies providing evidence for inflammatory mechanisms mediating both depressive-like behavior during separation as well as sensitization of stress responsiveness such as is thought to lead to increased vulnerability to depression at later ages. Finally, we discuss recent complementary work in adult monkeys that suggests cross-species generalizability of broad principles derived from the guinea pig experiments. Overall, the findings provide experimental support for human research implicating inflammatory mechanisms in the development of increased stress responsiveness and vulnerability to depression following attachment disruption and other forms of early-life stress. Specifically, the findings suggest inflammatory mechanisms may set in motion a cascade of underlying processes that mediate later increased stress responsiveness and, therefore, depression susceptibility. Frontiers Media S.A. 2019-01-07 /pmc/articles/PMC6330302/ /pubmed/30666192 http://dx.doi.org/10.3389/fnbeh.2018.00314 Text en Copyright © 2019 Hennessy, Schiml, Berberich, Beasley and Deak. 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) and the copyright owner(s) 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
Hennessy, Michael B.
Schiml, Patricia A.
Berberich, Katelyn
Beasley, Nicole L.
Deak, Terrence
Early Attachment Disruption, Inflammation, and Vulnerability for Depression in Rodent and Primate Models
title Early Attachment Disruption, Inflammation, and Vulnerability for Depression in Rodent and Primate Models
title_full Early Attachment Disruption, Inflammation, and Vulnerability for Depression in Rodent and Primate Models
title_fullStr Early Attachment Disruption, Inflammation, and Vulnerability for Depression in Rodent and Primate Models
title_full_unstemmed Early Attachment Disruption, Inflammation, and Vulnerability for Depression in Rodent and Primate Models
title_short Early Attachment Disruption, Inflammation, and Vulnerability for Depression in Rodent and Primate Models
title_sort early attachment disruption, inflammation, and vulnerability for depression in rodent and primate models
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330302/
https://www.ncbi.nlm.nih.gov/pubmed/30666192
http://dx.doi.org/10.3389/fnbeh.2018.00314
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