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Downregulation of microRNA‐330‐5p induces manic‐like behaviors in REM sleep‐deprived rats by enhancing tyrosine hydroxylase expression

AIM: In our pilot study, we found an increase in tyrosine hydroxylase (Th) mRNA expression in the prefrontal cortex of 72‐h REM sleep‐deprived (SD) rats, a mania model. Additionally, the expression levels of miR‐325‐3p, miR‐326‐3p, and miR‐330‐5p, the predicted target miRNAs on TH, were significantl...

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Autores principales: Leem, Kang Hyun, Kim, Sanga, Kim, Hee Won, Park, Hae Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173715/
https://www.ncbi.nlm.nih.gov/pubmed/36794530
http://dx.doi.org/10.1111/cns.14121
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author Leem, Kang Hyun
Kim, Sanga
Kim, Hee Won
Park, Hae Jeong
author_facet Leem, Kang Hyun
Kim, Sanga
Kim, Hee Won
Park, Hae Jeong
author_sort Leem, Kang Hyun
collection PubMed
description AIM: In our pilot study, we found an increase in tyrosine hydroxylase (Th) mRNA expression in the prefrontal cortex of 72‐h REM sleep‐deprived (SD) rats, a mania model. Additionally, the expression levels of miR‐325‐3p, miR‐326‐3p, and miR‐330‐5p, the predicted target miRNAs on TH, were significantly decreased. Based on these results, in this study, we investigated whether miRNA‐325‐3p, miR‐326‐3p, and miR‐330‐5p modulate TH and manic‐like behaviors in SD rats. METHODS: Manic‐like behaviors were assessed using the open field test (OFT) and elevated plus‐maze (EPM) test. The direct binding activity of miRNAs to the 3′‐untranslated region (3′‐UTR) of the Th gene was measured in HEK‐293 cells using a luciferase reporter system. We also examined mRNA and protein expression of TH after intracerebroventricular (ICV) injection of miR‐330‐5p agomir to SD rats, along with manic‐like behaviors. RESULTS: We observed an upregulation in mRNA and protein expression of TH and downregulation in miRNA‐325‐3p, miR‐326‐3p, and miR‐330‐5p expressions in the prefrontal cortex of SD rats, together with increased manic‐like behaviors. The luciferase reporter assay showed that miR‐330‐5p could repress TH expression through direct binding to its target site in the 3′‐UTR of Th, whereas miR‐326‐3p and miR‐330‐5p could not. In addition, ICV injection of miR‐330‐5p agomir alleviated the increase in TH expression in the prefrontal cortex of SD rats and manic‐like behaviors. CONCLUSIONS: TH expression regulation through miR‐330‐5p may be implicated in the pathophysiology of mania in SD rats.
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spelling pubmed-101737152023-05-12 Downregulation of microRNA‐330‐5p induces manic‐like behaviors in REM sleep‐deprived rats by enhancing tyrosine hydroxylase expression Leem, Kang Hyun Kim, Sanga Kim, Hee Won Park, Hae Jeong CNS Neurosci Ther Original Articles AIM: In our pilot study, we found an increase in tyrosine hydroxylase (Th) mRNA expression in the prefrontal cortex of 72‐h REM sleep‐deprived (SD) rats, a mania model. Additionally, the expression levels of miR‐325‐3p, miR‐326‐3p, and miR‐330‐5p, the predicted target miRNAs on TH, were significantly decreased. Based on these results, in this study, we investigated whether miRNA‐325‐3p, miR‐326‐3p, and miR‐330‐5p modulate TH and manic‐like behaviors in SD rats. METHODS: Manic‐like behaviors were assessed using the open field test (OFT) and elevated plus‐maze (EPM) test. The direct binding activity of miRNAs to the 3′‐untranslated region (3′‐UTR) of the Th gene was measured in HEK‐293 cells using a luciferase reporter system. We also examined mRNA and protein expression of TH after intracerebroventricular (ICV) injection of miR‐330‐5p agomir to SD rats, along with manic‐like behaviors. RESULTS: We observed an upregulation in mRNA and protein expression of TH and downregulation in miRNA‐325‐3p, miR‐326‐3p, and miR‐330‐5p expressions in the prefrontal cortex of SD rats, together with increased manic‐like behaviors. The luciferase reporter assay showed that miR‐330‐5p could repress TH expression through direct binding to its target site in the 3′‐UTR of Th, whereas miR‐326‐3p and miR‐330‐5p could not. In addition, ICV injection of miR‐330‐5p agomir alleviated the increase in TH expression in the prefrontal cortex of SD rats and manic‐like behaviors. CONCLUSIONS: TH expression regulation through miR‐330‐5p may be implicated in the pathophysiology of mania in SD rats. John Wiley and Sons Inc. 2023-02-16 /pmc/articles/PMC10173715/ /pubmed/36794530 http://dx.doi.org/10.1111/cns.14121 Text en © 2023 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Leem, Kang Hyun
Kim, Sanga
Kim, Hee Won
Park, Hae Jeong
Downregulation of microRNA‐330‐5p induces manic‐like behaviors in REM sleep‐deprived rats by enhancing tyrosine hydroxylase expression
title Downregulation of microRNA‐330‐5p induces manic‐like behaviors in REM sleep‐deprived rats by enhancing tyrosine hydroxylase expression
title_full Downregulation of microRNA‐330‐5p induces manic‐like behaviors in REM sleep‐deprived rats by enhancing tyrosine hydroxylase expression
title_fullStr Downregulation of microRNA‐330‐5p induces manic‐like behaviors in REM sleep‐deprived rats by enhancing tyrosine hydroxylase expression
title_full_unstemmed Downregulation of microRNA‐330‐5p induces manic‐like behaviors in REM sleep‐deprived rats by enhancing tyrosine hydroxylase expression
title_short Downregulation of microRNA‐330‐5p induces manic‐like behaviors in REM sleep‐deprived rats by enhancing tyrosine hydroxylase expression
title_sort downregulation of microrna‐330‐5p induces manic‐like behaviors in rem sleep‐deprived rats by enhancing tyrosine hydroxylase expression
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173715/
https://www.ncbi.nlm.nih.gov/pubmed/36794530
http://dx.doi.org/10.1111/cns.14121
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