Vasoactive intestinal polypeptide plasma levels associated with affective symptoms and brain structure and function in healthy females

Abstract Vasoactive intestinal polypeptide (VIP) is a neuroendocrine peptide distributed throughout the human body, including the CNS, where it is particularly abundant in brain regions associated with anxiety and depression. Based on earlier studies indicating that peripheral VIP may cross through...

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Autores principales: Rozalyn A. Simon, Nawroz Barazanji, Michael P. Jones, Olga Bednarska, Adriane Icenhour, Maria Engström, J. Paul Hamilton, Åsa V. Keita, Susanna Walter
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/678a1728f56d44d58d47f1c9be74aef2
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spelling oai:doaj.org-article:678a1728f56d44d58d47f1c9be74aef22021-12-02T14:12:46ZVasoactive intestinal polypeptide plasma levels associated with affective symptoms and brain structure and function in healthy females10.1038/s41598-020-80873-22045-2322https://doaj.org/article/678a1728f56d44d58d47f1c9be74aef22021-01-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-80873-2https://doaj.org/toc/2045-2322Abstract Vasoactive intestinal polypeptide (VIP) is a neuroendocrine peptide distributed throughout the human body, including the CNS, where it is particularly abundant in brain regions associated with anxiety and depression. Based on earlier studies indicating that peripheral VIP may cross through the blood–brain barrier, we hypothesized plasma VIP levels to be associated with symptoms of anxiety and depression, as well as brain volume and resting-state functional connectivity in the amygdala, hippocampus, parahippocampus, and orbitofrontal cortex. Plasma VIP concentrations and anxiety/depression symptoms were measured in 37 healthy females. Functional and structural magnetic resonance imaging were used to evaluate functional connectivity and brain volume respectively, and their associations with VIP concentrations within brain regions associated with anxiety and depression. Negative correlations were found between VIP levels and symptoms of anxiety (r = − 0.44, p = 0.002) and depression (r = − 0.50, p = 0.001). Functional connectivity demonstrated significant VIP-dependent positive associations between the amygdala seed region with both the right parahippocampus (t (33) = 3.1, p FDR  = 0.02) and right lateral orbitofrontal cortex (OFC; t (33) = 2.9, p FDR  = 0.02). Moreover, VIP concentrations were significantly, positively correlated with brain volume in the left amygdala (r = 0.28, p = 0.007) and left lateral OFC (r = 0.29, p = 0.004). The present findings highlight a potential role for VIP in the neurobiology of affective symptoms.Rozalyn A. SimonNawroz BarazanjiMichael P. JonesOlga BednarskaAdriane IcenhourMaria EngströmJ. Paul HamiltonÅsa V. KeitaSusanna WalterNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Rozalyn A. Simon
Nawroz Barazanji
Michael P. Jones
Olga Bednarska
Adriane Icenhour
Maria Engström
J. Paul Hamilton
Åsa V. Keita
Susanna Walter
Vasoactive intestinal polypeptide plasma levels associated with affective symptoms and brain structure and function in healthy females
description Abstract Vasoactive intestinal polypeptide (VIP) is a neuroendocrine peptide distributed throughout the human body, including the CNS, where it is particularly abundant in brain regions associated with anxiety and depression. Based on earlier studies indicating that peripheral VIP may cross through the blood–brain barrier, we hypothesized plasma VIP levels to be associated with symptoms of anxiety and depression, as well as brain volume and resting-state functional connectivity in the amygdala, hippocampus, parahippocampus, and orbitofrontal cortex. Plasma VIP concentrations and anxiety/depression symptoms were measured in 37 healthy females. Functional and structural magnetic resonance imaging were used to evaluate functional connectivity and brain volume respectively, and their associations with VIP concentrations within brain regions associated with anxiety and depression. Negative correlations were found between VIP levels and symptoms of anxiety (r = − 0.44, p = 0.002) and depression (r = − 0.50, p = 0.001). Functional connectivity demonstrated significant VIP-dependent positive associations between the amygdala seed region with both the right parahippocampus (t (33) = 3.1, p FDR  = 0.02) and right lateral orbitofrontal cortex (OFC; t (33) = 2.9, p FDR  = 0.02). Moreover, VIP concentrations were significantly, positively correlated with brain volume in the left amygdala (r = 0.28, p = 0.007) and left lateral OFC (r = 0.29, p = 0.004). The present findings highlight a potential role for VIP in the neurobiology of affective symptoms.
format article
author Rozalyn A. Simon
Nawroz Barazanji
Michael P. Jones
Olga Bednarska
Adriane Icenhour
Maria Engström
J. Paul Hamilton
Åsa V. Keita
Susanna Walter
author_facet Rozalyn A. Simon
Nawroz Barazanji
Michael P. Jones
Olga Bednarska
Adriane Icenhour
Maria Engström
J. Paul Hamilton
Åsa V. Keita
Susanna Walter
author_sort Rozalyn A. Simon
title Vasoactive intestinal polypeptide plasma levels associated with affective symptoms and brain structure and function in healthy females
title_short Vasoactive intestinal polypeptide plasma levels associated with affective symptoms and brain structure and function in healthy females
title_full Vasoactive intestinal polypeptide plasma levels associated with affective symptoms and brain structure and function in healthy females
title_fullStr Vasoactive intestinal polypeptide plasma levels associated with affective symptoms and brain structure and function in healthy females
title_full_unstemmed Vasoactive intestinal polypeptide plasma levels associated with affective symptoms and brain structure and function in healthy females
title_sort vasoactive intestinal polypeptide plasma levels associated with affective symptoms and brain structure and function in healthy females
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/678a1728f56d44d58d47f1c9be74aef2
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