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Elevated cerebrospinal fluid 5-hydroxyindoleacetic acid in macaques following early life stress and inverse association with hippocampal volume: preliminary implications for serotonin-related function in mood and anxiety disorders

Background: Early life stress (ELS) is cited as a risk for mood and anxiety disorders, potentially through altered serotonin neurotransmission. We examined the effects of ELS, utilizing the variable foraging demand (VFD) macaque model, on adolescent monoamine metabolites. We sought to replicate an i...

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Autores principales: Coplan, Jeremy D., Fulton, Sasha L., Reiner, Wade, Jackowski, Andrea, Panthangi, Venkatesh, Perera, Tarique D., Gorman, Jack M., Huang, Yung-yu, Tang, Cheuk Y., Hof, Patrick R., Kaffman, Arie, Dwork, Andrew J., Mathew, Sanjay J., Kaufman, Joan, Mann, J. John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274982/
https://www.ncbi.nlm.nih.gov/pubmed/25566007
http://dx.doi.org/10.3389/fnbeh.2014.00440
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author Coplan, Jeremy D.
Fulton, Sasha L.
Reiner, Wade
Jackowski, Andrea
Panthangi, Venkatesh
Perera, Tarique D.
Gorman, Jack M.
Huang, Yung-yu
Tang, Cheuk Y.
Hof, Patrick R.
Kaffman, Arie
Dwork, Andrew J.
Mathew, Sanjay J.
Kaufman, Joan
Mann, J. John
author_facet Coplan, Jeremy D.
Fulton, Sasha L.
Reiner, Wade
Jackowski, Andrea
Panthangi, Venkatesh
Perera, Tarique D.
Gorman, Jack M.
Huang, Yung-yu
Tang, Cheuk Y.
Hof, Patrick R.
Kaffman, Arie
Dwork, Andrew J.
Mathew, Sanjay J.
Kaufman, Joan
Mann, J. John
author_sort Coplan, Jeremy D.
collection PubMed
description Background: Early life stress (ELS) is cited as a risk for mood and anxiety disorders, potentially through altered serotonin neurotransmission. We examined the effects of ELS, utilizing the variable foraging demand (VFD) macaque model, on adolescent monoamine metabolites. We sought to replicate an increase in cerebrospinal fluid (CSF) 5-hydroxyindoleacetic acid (5-HIAA) observed in two previous VFD cohorts. We hypothesized that elevated cisternal 5-HIAA was associated with reduced neurotrophic effects, conceivably due to excessive negative feedback at somatodendritic 5-HT(1A) autoreceptors. A putatively decreased serotonin neurotransmission would be reflected by reductions in hippocampal volume and white matter (WM) fractional anisotropy (FA). Methods: When infants were 2–6 months of age, bonnet macaque mothers were exposed to VFD. We employed cisternal CSF taps to measure monoamine metabolites in VFD (N = 22) and non-VFD (N = 14) offspring (mean age = 2.61 years). Metabolites were correlated with hippocampal volume obtained by MRI and WM FA by diffusion tensor imaging in young adulthood in 17 males [10 VFD (mean age = 4.57 years)]. Results: VFD subjects exhibited increased CSF 5-HIAA compared to non-VFD controls. An inverse correlation between right hippocampal volume and 5-HIAA was noted in VFD- but not controls. CSF HVA and MHPG correlated inversely with hippocampal volume only in VFD. CSF 5-HIAA correlated inversely with FA of the WM tracts of the anterior limb of the internal capsule (ALIC) only in VFD. Conclusions: Elevated cisternal 5-HIAA in VFD may reflect increased dorsal raphe serotonin, potentially inducing excessive autoreceptor activation, inducing a putative serotonin deficit in terminal fields. Resultant reductions in neurotrophic activity are reflected by smaller right hippocampal volume. Convergent evidence of reduced neurotrophic activity in association with high CSF 5-HIAA in VFD was reflected by reduced FA of the ALIC.
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spelling pubmed-42749822015-01-06 Elevated cerebrospinal fluid 5-hydroxyindoleacetic acid in macaques following early life stress and inverse association with hippocampal volume: preliminary implications for serotonin-related function in mood and anxiety disorders Coplan, Jeremy D. Fulton, Sasha L. Reiner, Wade Jackowski, Andrea Panthangi, Venkatesh Perera, Tarique D. Gorman, Jack M. Huang, Yung-yu Tang, Cheuk Y. Hof, Patrick R. Kaffman, Arie Dwork, Andrew J. Mathew, Sanjay J. Kaufman, Joan Mann, J. John Front Behav Neurosci Neuroscience Background: Early life stress (ELS) is cited as a risk for mood and anxiety disorders, potentially through altered serotonin neurotransmission. We examined the effects of ELS, utilizing the variable foraging demand (VFD) macaque model, on adolescent monoamine metabolites. We sought to replicate an increase in cerebrospinal fluid (CSF) 5-hydroxyindoleacetic acid (5-HIAA) observed in two previous VFD cohorts. We hypothesized that elevated cisternal 5-HIAA was associated with reduced neurotrophic effects, conceivably due to excessive negative feedback at somatodendritic 5-HT(1A) autoreceptors. A putatively decreased serotonin neurotransmission would be reflected by reductions in hippocampal volume and white matter (WM) fractional anisotropy (FA). Methods: When infants were 2–6 months of age, bonnet macaque mothers were exposed to VFD. We employed cisternal CSF taps to measure monoamine metabolites in VFD (N = 22) and non-VFD (N = 14) offspring (mean age = 2.61 years). Metabolites were correlated with hippocampal volume obtained by MRI and WM FA by diffusion tensor imaging in young adulthood in 17 males [10 VFD (mean age = 4.57 years)]. Results: VFD subjects exhibited increased CSF 5-HIAA compared to non-VFD controls. An inverse correlation between right hippocampal volume and 5-HIAA was noted in VFD- but not controls. CSF HVA and MHPG correlated inversely with hippocampal volume only in VFD. CSF 5-HIAA correlated inversely with FA of the WM tracts of the anterior limb of the internal capsule (ALIC) only in VFD. Conclusions: Elevated cisternal 5-HIAA in VFD may reflect increased dorsal raphe serotonin, potentially inducing excessive autoreceptor activation, inducing a putative serotonin deficit in terminal fields. Resultant reductions in neurotrophic activity are reflected by smaller right hippocampal volume. Convergent evidence of reduced neurotrophic activity in association with high CSF 5-HIAA in VFD was reflected by reduced FA of the ALIC. Frontiers Media S.A. 2014-12-23 /pmc/articles/PMC4274982/ /pubmed/25566007 http://dx.doi.org/10.3389/fnbeh.2014.00440 Text en Copyright © 2014 Coplan, Fulton, Reiner, Jackowski, Panthangi, Perera, Gorman, Huang, Tang, Hof, Kaffman, Dwork, Mathew, Kaufman and Mann. 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.
Fulton, Sasha L.
Reiner, Wade
Jackowski, Andrea
Panthangi, Venkatesh
Perera, Tarique D.
Gorman, Jack M.
Huang, Yung-yu
Tang, Cheuk Y.
Hof, Patrick R.
Kaffman, Arie
Dwork, Andrew J.
Mathew, Sanjay J.
Kaufman, Joan
Mann, J. John
Elevated cerebrospinal fluid 5-hydroxyindoleacetic acid in macaques following early life stress and inverse association with hippocampal volume: preliminary implications for serotonin-related function in mood and anxiety disorders
title Elevated cerebrospinal fluid 5-hydroxyindoleacetic acid in macaques following early life stress and inverse association with hippocampal volume: preliminary implications for serotonin-related function in mood and anxiety disorders
title_full Elevated cerebrospinal fluid 5-hydroxyindoleacetic acid in macaques following early life stress and inverse association with hippocampal volume: preliminary implications for serotonin-related function in mood and anxiety disorders
title_fullStr Elevated cerebrospinal fluid 5-hydroxyindoleacetic acid in macaques following early life stress and inverse association with hippocampal volume: preliminary implications for serotonin-related function in mood and anxiety disorders
title_full_unstemmed Elevated cerebrospinal fluid 5-hydroxyindoleacetic acid in macaques following early life stress and inverse association with hippocampal volume: preliminary implications for serotonin-related function in mood and anxiety disorders
title_short Elevated cerebrospinal fluid 5-hydroxyindoleacetic acid in macaques following early life stress and inverse association with hippocampal volume: preliminary implications for serotonin-related function in mood and anxiety disorders
title_sort elevated cerebrospinal fluid 5-hydroxyindoleacetic acid in macaques following early life stress and inverse association with hippocampal volume: preliminary implications for serotonin-related function in mood and anxiety disorders
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274982/
https://www.ncbi.nlm.nih.gov/pubmed/25566007
http://dx.doi.org/10.3389/fnbeh.2014.00440
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