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Effect of Vitamin D(3) on Chemerin and Adiponectin Levels in Uterus of Polycystic Ovary Syndrome Rats
Background: Polycystic ovary syndrome (PCOS) is an endocrine disorder with disrupted uterus structure and function. A positive effect of vitamin D(3) (VD(3)) in female reproduction was observed. Chemerin (RARRES2) and adiponectin (ADIPOQ) are the main adipokines whose levels are altered in PCOS pati...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453942/ https://www.ncbi.nlm.nih.gov/pubmed/37626836 http://dx.doi.org/10.3390/cells12162026 |
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author | Pich, Karolina Rajewska, Jesika Kamińska, Kinga Tchurzyk, Marcelina Szlaga, Agata Sambak, Patryk Błasiak, Anna Grzesiak, Małgorzata Rak, Agnieszka |
author_facet | Pich, Karolina Rajewska, Jesika Kamińska, Kinga Tchurzyk, Marcelina Szlaga, Agata Sambak, Patryk Błasiak, Anna Grzesiak, Małgorzata Rak, Agnieszka |
author_sort | Pich, Karolina |
collection | PubMed |
description | Background: Polycystic ovary syndrome (PCOS) is an endocrine disorder with disrupted uterus structure and function. A positive effect of vitamin D(3) (VD(3)) in female reproduction was observed. Chemerin (RARRES2) and adiponectin (ADIPOQ) are the main adipokines whose levels are altered in PCOS patients. Therefore, the aim of this study was to investigate the impact of VD(3) supplementation on RARRES2 and ADIPOQ levels in the uterus of PCOS rats. Methods: We analyzed the plasma levels and uterine transcript and protein expression of RARRES2 and ADIPOQ and their receptors (CCRL2, CMKLR1, GPR1, and ADIPOR1 and ADIPOR2, respectively) in rats with letrozole-induced PCOS. Results: In control animals, VD(3) did not change plasma levels of both adipokines, while in PCOS rats supplemented with VD(3), they returned to control levels. The expression of RARRES2 and all investigated receptors increased in the uterus of VD(3)-treated rats; however, the levels of Rarres2 and Gpr1 genes remained unchanged. VD(3) supplementation decreased RARRES2, CMKLR1, and GPR1 but increased CCRL2 level to the control value. In the uterus of VD(3)-treated rats, the transcript and protein levels of ADIPOQ and both receptors ADIPOR1 increased. At the same time, VD(3) supplementation induced an increase in Adipoq, Adipor1, and Adipor2 gene expression and restored protein levels to control level values. Conclusions: our findings indicate a new mechanism of VD(3) action in the uterine physiology of PCOS rats. |
format | Online Article Text |
id | pubmed-10453942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104539422023-08-26 Effect of Vitamin D(3) on Chemerin and Adiponectin Levels in Uterus of Polycystic Ovary Syndrome Rats Pich, Karolina Rajewska, Jesika Kamińska, Kinga Tchurzyk, Marcelina Szlaga, Agata Sambak, Patryk Błasiak, Anna Grzesiak, Małgorzata Rak, Agnieszka Cells Article Background: Polycystic ovary syndrome (PCOS) is an endocrine disorder with disrupted uterus structure and function. A positive effect of vitamin D(3) (VD(3)) in female reproduction was observed. Chemerin (RARRES2) and adiponectin (ADIPOQ) are the main adipokines whose levels are altered in PCOS patients. Therefore, the aim of this study was to investigate the impact of VD(3) supplementation on RARRES2 and ADIPOQ levels in the uterus of PCOS rats. Methods: We analyzed the plasma levels and uterine transcript and protein expression of RARRES2 and ADIPOQ and their receptors (CCRL2, CMKLR1, GPR1, and ADIPOR1 and ADIPOR2, respectively) in rats with letrozole-induced PCOS. Results: In control animals, VD(3) did not change plasma levels of both adipokines, while in PCOS rats supplemented with VD(3), they returned to control levels. The expression of RARRES2 and all investigated receptors increased in the uterus of VD(3)-treated rats; however, the levels of Rarres2 and Gpr1 genes remained unchanged. VD(3) supplementation decreased RARRES2, CMKLR1, and GPR1 but increased CCRL2 level to the control value. In the uterus of VD(3)-treated rats, the transcript and protein levels of ADIPOQ and both receptors ADIPOR1 increased. At the same time, VD(3) supplementation induced an increase in Adipoq, Adipor1, and Adipor2 gene expression and restored protein levels to control level values. Conclusions: our findings indicate a new mechanism of VD(3) action in the uterine physiology of PCOS rats. MDPI 2023-08-08 /pmc/articles/PMC10453942/ /pubmed/37626836 http://dx.doi.org/10.3390/cells12162026 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pich, Karolina Rajewska, Jesika Kamińska, Kinga Tchurzyk, Marcelina Szlaga, Agata Sambak, Patryk Błasiak, Anna Grzesiak, Małgorzata Rak, Agnieszka Effect of Vitamin D(3) on Chemerin and Adiponectin Levels in Uterus of Polycystic Ovary Syndrome Rats |
title | Effect of Vitamin D(3) on Chemerin and Adiponectin Levels in Uterus of Polycystic Ovary Syndrome Rats |
title_full | Effect of Vitamin D(3) on Chemerin and Adiponectin Levels in Uterus of Polycystic Ovary Syndrome Rats |
title_fullStr | Effect of Vitamin D(3) on Chemerin and Adiponectin Levels in Uterus of Polycystic Ovary Syndrome Rats |
title_full_unstemmed | Effect of Vitamin D(3) on Chemerin and Adiponectin Levels in Uterus of Polycystic Ovary Syndrome Rats |
title_short | Effect of Vitamin D(3) on Chemerin and Adiponectin Levels in Uterus of Polycystic Ovary Syndrome Rats |
title_sort | effect of vitamin d(3) on chemerin and adiponectin levels in uterus of polycystic ovary syndrome rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453942/ https://www.ncbi.nlm.nih.gov/pubmed/37626836 http://dx.doi.org/10.3390/cells12162026 |
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