Dopaminergic and cholinergic modulation of the amygdala is altered in female mice with oestrogen receptor β deprivation

Abstract The amygdala is modulated by dopaminergic and cholinergic neurotransmission, and this modulation is altered in mood disorders. Therefore, this study was designed to evaluate the presence/absence of quantitative alterations in the expression of main dopaminergic and cholinergic markers in th...

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Main Authors: Daniel Kalinowski, Krystyna Bogus-Nowakowska, Anna Kozłowska, Maciej Równiak
Format: Article
Language:English
Published: Nature Portfolio 2023-01-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-28069-2
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author Daniel Kalinowski
Krystyna Bogus-Nowakowska
Anna Kozłowska
Maciej Równiak
author_facet Daniel Kalinowski
Krystyna Bogus-Nowakowska
Anna Kozłowska
Maciej Równiak
author_sort Daniel Kalinowski
collection DOAJ
description Abstract The amygdala is modulated by dopaminergic and cholinergic neurotransmission, and this modulation is altered in mood disorders. Therefore, this study was designed to evaluate the presence/absence of quantitative alterations in the expression of main dopaminergic and cholinergic markers in the amygdala of mice with oestrogen receptor β (ERβ) knock-out which exhibit increased anxiety, using immunohistochemistry and quantitative methods. Such alterations could either contribute to increased anxiety or be a compensatory mechanism for reducing anxiety. The results show that among dopaminergic markers, the expression of tyrosine hydroxylase (TH), dopamine transporter (DAT) and dopamine D2-like receptor (DA2) is significantly elevated in the amygdala of mice with ERβ deprivation when compared to matched controls, whereas the content of dopamine D1-like receptor (DA1) is not altered by ERβ knock-out. In the case of cholinergic markers, muscarinic acetylcholine type 1 receptor (AChRM1) and alpha-7 nicotinic acetylcholine receptor (AChRα7) display overexpression while the content of acetylcholinesterase (AChE) and vesicular acetylcholine transporter (VAChT) remains unchanged. In conclusion, in the amygdala of ERβ knock-out female the dopaminergic and cholinergic signalling is altered, however, to determine the exact role of ERβ in the anxiety-related behaviour further studies are required.
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spelling doaj.art-fb1fbcb6581f4b46877eb11f7d160ac02023-01-22T12:14:06ZengNature PortfolioScientific Reports2045-23222023-01-0113111810.1038/s41598-023-28069-2Dopaminergic and cholinergic modulation of the amygdala is altered in female mice with oestrogen receptor β deprivationDaniel Kalinowski0Krystyna Bogus-Nowakowska1Anna Kozłowska2Maciej Równiak3Department of Animal Anatomy and Physiology, Faculty of Biology and Biotechnology, University of Warmia and Mazury in OlsztynDepartment of Animal Anatomy and Physiology, Faculty of Biology and Biotechnology, University of Warmia and Mazury in OlsztynDepartment of Human Physiology and Pathophysiology, School of Medicine, University of Warmia and Mazury in OlsztynDepartment of Animal Anatomy and Physiology, Faculty of Biology and Biotechnology, University of Warmia and Mazury in OlsztynAbstract The amygdala is modulated by dopaminergic and cholinergic neurotransmission, and this modulation is altered in mood disorders. Therefore, this study was designed to evaluate the presence/absence of quantitative alterations in the expression of main dopaminergic and cholinergic markers in the amygdala of mice with oestrogen receptor β (ERβ) knock-out which exhibit increased anxiety, using immunohistochemistry and quantitative methods. Such alterations could either contribute to increased anxiety or be a compensatory mechanism for reducing anxiety. The results show that among dopaminergic markers, the expression of tyrosine hydroxylase (TH), dopamine transporter (DAT) and dopamine D2-like receptor (DA2) is significantly elevated in the amygdala of mice with ERβ deprivation when compared to matched controls, whereas the content of dopamine D1-like receptor (DA1) is not altered by ERβ knock-out. In the case of cholinergic markers, muscarinic acetylcholine type 1 receptor (AChRM1) and alpha-7 nicotinic acetylcholine receptor (AChRα7) display overexpression while the content of acetylcholinesterase (AChE) and vesicular acetylcholine transporter (VAChT) remains unchanged. In conclusion, in the amygdala of ERβ knock-out female the dopaminergic and cholinergic signalling is altered, however, to determine the exact role of ERβ in the anxiety-related behaviour further studies are required.https://doi.org/10.1038/s41598-023-28069-2
spellingShingle Daniel Kalinowski
Krystyna Bogus-Nowakowska
Anna Kozłowska
Maciej Równiak
Dopaminergic and cholinergic modulation of the amygdala is altered in female mice with oestrogen receptor β deprivation
Scientific Reports
title Dopaminergic and cholinergic modulation of the amygdala is altered in female mice with oestrogen receptor β deprivation
title_full Dopaminergic and cholinergic modulation of the amygdala is altered in female mice with oestrogen receptor β deprivation
title_fullStr Dopaminergic and cholinergic modulation of the amygdala is altered in female mice with oestrogen receptor β deprivation
title_full_unstemmed Dopaminergic and cholinergic modulation of the amygdala is altered in female mice with oestrogen receptor β deprivation
title_short Dopaminergic and cholinergic modulation of the amygdala is altered in female mice with oestrogen receptor β deprivation
title_sort dopaminergic and cholinergic modulation of the amygdala is altered in female mice with oestrogen receptor β deprivation
url https://doi.org/10.1038/s41598-023-28069-2
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AT annakozłowska dopaminergicandcholinergicmodulationoftheamygdalaisalteredinfemalemicewithoestrogenreceptorbdeprivation
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