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The effect of valproic acid on SLC5A8 expression in gonad-intact and gonadectomized rat thymocytes

BACKGROUND: Valproic acid (VPA) pharmacological mechanisms are related to the anti-inflammatory and anti-viral effects. VPA is a histone deacetylases inhibitor and serves a role in its immunomodulatory impacts. VPA has complex effects on immune cell’s mitochondrial metabolism. The SLC5A8 transporter...

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Autores principales: Juknevičienė, Milda, Balnytė, Ingrida, Valančiūtė, Angelija, Stanevičiūtė, Jūratė, Sužiedėlis, Kęstutis, Stakišaitis, Donatas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819739/
https://www.ncbi.nlm.nih.gov/pubmed/35120418
http://dx.doi.org/10.1177/20587384211051954
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author Juknevičienė, Milda
Balnytė, Ingrida
Valančiūtė, Angelija
Stanevičiūtė, Jūratė
Sužiedėlis, Kęstutis
Stakišaitis, Donatas
author_facet Juknevičienė, Milda
Balnytė, Ingrida
Valančiūtė, Angelija
Stanevičiūtė, Jūratė
Sužiedėlis, Kęstutis
Stakišaitis, Donatas
author_sort Juknevičienė, Milda
collection PubMed
description BACKGROUND: Valproic acid (VPA) pharmacological mechanisms are related to the anti-inflammatory and anti-viral effects. VPA is a histone deacetylases inhibitor and serves a role in its immunomodulatory impacts. VPA has complex effects on immune cell’s mitochondrial metabolism. The SLC5A8 transporter of short fatty acids has an active role in regulating mitochondrial metabolism. The study aimed to investigate whether SLC5A8 expresses the sex-related difference and how SLC5A8 expression depends on gonadal hormones, VPA treatment, and NKCC1 expression in rat thymocytes. METHODS: Control groups and VPA-treated gonad-intact and gonadectomized Wistar male and female rats were investigated (n = 6 in a group). The VPA 300 mg/kg/day in drinking water was given for 4 weeks. The SLC5A8 (Slc5a8 gene) and NKCC1 (Slc12a2 gene) RNA expressions were determined by the RT-PCR method. RESULTS: The higher Slc5a8 expression was found in the gonad-intact males than respective females (p = 0.004). VPA treatment decreased the Slc5a8 expression in gonad-intact and castrated males (p = 0.02 and p = 0.03, respectively), and increased in gonad-intact female rats compared to their control (p = 0.03). No significant difference in the Slc5a8 expression between the ovariectomized female control and VPA-treated females was determined (p > 0.05). VPA treatment alters the correlation between Slc5a8 and Slc12a2 gene expression in thymocytes of gonad-intact rats. CONCLUSION: VPA effect on the Slc5a8 expression in rat thymocytes is gender- and gonadal hormone-dependent.
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spelling pubmed-88197392022-02-08 The effect of valproic acid on SLC5A8 expression in gonad-intact and gonadectomized rat thymocytes Juknevičienė, Milda Balnytė, Ingrida Valančiūtė, Angelija Stanevičiūtė, Jūratė Sužiedėlis, Kęstutis Stakišaitis, Donatas Int J Immunopathol Pharmacol Original Research Article BACKGROUND: Valproic acid (VPA) pharmacological mechanisms are related to the anti-inflammatory and anti-viral effects. VPA is a histone deacetylases inhibitor and serves a role in its immunomodulatory impacts. VPA has complex effects on immune cell’s mitochondrial metabolism. The SLC5A8 transporter of short fatty acids has an active role in regulating mitochondrial metabolism. The study aimed to investigate whether SLC5A8 expresses the sex-related difference and how SLC5A8 expression depends on gonadal hormones, VPA treatment, and NKCC1 expression in rat thymocytes. METHODS: Control groups and VPA-treated gonad-intact and gonadectomized Wistar male and female rats were investigated (n = 6 in a group). The VPA 300 mg/kg/day in drinking water was given for 4 weeks. The SLC5A8 (Slc5a8 gene) and NKCC1 (Slc12a2 gene) RNA expressions were determined by the RT-PCR method. RESULTS: The higher Slc5a8 expression was found in the gonad-intact males than respective females (p = 0.004). VPA treatment decreased the Slc5a8 expression in gonad-intact and castrated males (p = 0.02 and p = 0.03, respectively), and increased in gonad-intact female rats compared to their control (p = 0.03). No significant difference in the Slc5a8 expression between the ovariectomized female control and VPA-treated females was determined (p > 0.05). VPA treatment alters the correlation between Slc5a8 and Slc12a2 gene expression in thymocytes of gonad-intact rats. CONCLUSION: VPA effect on the Slc5a8 expression in rat thymocytes is gender- and gonadal hormone-dependent. SAGE Publications 2022-02-04 /pmc/articles/PMC8819739/ /pubmed/35120418 http://dx.doi.org/10.1177/20587384211051954 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Article
Juknevičienė, Milda
Balnytė, Ingrida
Valančiūtė, Angelija
Stanevičiūtė, Jūratė
Sužiedėlis, Kęstutis
Stakišaitis, Donatas
The effect of valproic acid on SLC5A8 expression in gonad-intact and gonadectomized rat thymocytes
title The effect of valproic acid on SLC5A8 expression in gonad-intact and gonadectomized rat thymocytes
title_full The effect of valproic acid on SLC5A8 expression in gonad-intact and gonadectomized rat thymocytes
title_fullStr The effect of valproic acid on SLC5A8 expression in gonad-intact and gonadectomized rat thymocytes
title_full_unstemmed The effect of valproic acid on SLC5A8 expression in gonad-intact and gonadectomized rat thymocytes
title_short The effect of valproic acid on SLC5A8 expression in gonad-intact and gonadectomized rat thymocytes
title_sort effect of valproic acid on slc5a8 expression in gonad-intact and gonadectomized rat thymocytes
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819739/
https://www.ncbi.nlm.nih.gov/pubmed/35120418
http://dx.doi.org/10.1177/20587384211051954
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