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Antipsychotics increase steroidogenic enzyme gene expression in the rat brainstem
BACKGROUND: Neurosteroids are involved in several important brain functions and have recently been considered novel players in the mechanic actions of neuropsychiatric drugs. There are no reports of murine studies focusing on the effect of chronic neurosteroid treatment in parallel with antipsychoti...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825390/ https://www.ncbi.nlm.nih.gov/pubmed/34797492 http://dx.doi.org/10.1007/s11033-021-06943-4 |
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author | Bogus, Katarzyna Żarczyńska, Małgorzata Pałasz, Artur Suszka-Świtek, Aleksandra Worthington, John J. Krzystanek, Marek Żarczyński, Piotr |
author_facet | Bogus, Katarzyna Żarczyńska, Małgorzata Pałasz, Artur Suszka-Świtek, Aleksandra Worthington, John J. Krzystanek, Marek Żarczyński, Piotr |
author_sort | Bogus, Katarzyna |
collection | PubMed |
description | BACKGROUND: Neurosteroids are involved in several important brain functions and have recently been considered novel players in the mechanic actions of neuropsychiatric drugs. There are no reports of murine studies focusing on the effect of chronic neurosteroid treatment in parallel with antipsychotics on key steroidogenic enzyme expression and we therefore focused on steroidogenic enzyme gene expression in the brainstem of rats chronically treated with olanzapine and haloperidol. METHODS AND RESULTS: Studies were carried out on adult, male Sprague–Dawley rats which were divided into 3 groups: control and experimental animals treated with olanzapine or haloperidol. Total mRNA was isolated from homogenized brainstem samples for RealTime-PCR to estimate gene expression of related aromatase, 3β-HSD and P450scc. Long-term treatment with the selected antipsychotics was reflected in the modulation of steroidogenic enzyme gene expression in the examined brainstem region; with both olanzapine and haloperidol increasing aromatase, 3β-HSD and P450scc gene expression. CONCLUSIONS: The present findings shed new light on the pharmacology of antipsychotics and suggest the existence of possible regulatory interplay between neuroleptic action and steroidogenesis at the level of brainstem neuronal centres. |
format | Online Article Text |
id | pubmed-8825390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-88253902022-02-23 Antipsychotics increase steroidogenic enzyme gene expression in the rat brainstem Bogus, Katarzyna Żarczyńska, Małgorzata Pałasz, Artur Suszka-Świtek, Aleksandra Worthington, John J. Krzystanek, Marek Żarczyński, Piotr Mol Biol Rep Short Communication BACKGROUND: Neurosteroids are involved in several important brain functions and have recently been considered novel players in the mechanic actions of neuropsychiatric drugs. There are no reports of murine studies focusing on the effect of chronic neurosteroid treatment in parallel with antipsychotics on key steroidogenic enzyme expression and we therefore focused on steroidogenic enzyme gene expression in the brainstem of rats chronically treated with olanzapine and haloperidol. METHODS AND RESULTS: Studies were carried out on adult, male Sprague–Dawley rats which were divided into 3 groups: control and experimental animals treated with olanzapine or haloperidol. Total mRNA was isolated from homogenized brainstem samples for RealTime-PCR to estimate gene expression of related aromatase, 3β-HSD and P450scc. Long-term treatment with the selected antipsychotics was reflected in the modulation of steroidogenic enzyme gene expression in the examined brainstem region; with both olanzapine and haloperidol increasing aromatase, 3β-HSD and P450scc gene expression. CONCLUSIONS: The present findings shed new light on the pharmacology of antipsychotics and suggest the existence of possible regulatory interplay between neuroleptic action and steroidogenesis at the level of brainstem neuronal centres. Springer Netherlands 2021-11-19 2022 /pmc/articles/PMC8825390/ /pubmed/34797492 http://dx.doi.org/10.1007/s11033-021-06943-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Short Communication Bogus, Katarzyna Żarczyńska, Małgorzata Pałasz, Artur Suszka-Świtek, Aleksandra Worthington, John J. Krzystanek, Marek Żarczyński, Piotr Antipsychotics increase steroidogenic enzyme gene expression in the rat brainstem |
title | Antipsychotics increase steroidogenic enzyme gene expression in the rat brainstem |
title_full | Antipsychotics increase steroidogenic enzyme gene expression in the rat brainstem |
title_fullStr | Antipsychotics increase steroidogenic enzyme gene expression in the rat brainstem |
title_full_unstemmed | Antipsychotics increase steroidogenic enzyme gene expression in the rat brainstem |
title_short | Antipsychotics increase steroidogenic enzyme gene expression in the rat brainstem |
title_sort | antipsychotics increase steroidogenic enzyme gene expression in the rat brainstem |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825390/ https://www.ncbi.nlm.nih.gov/pubmed/34797492 http://dx.doi.org/10.1007/s11033-021-06943-4 |
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