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Follicle stimulating hormone promotes production of renin through its receptor in juxtaglomerular cells of kidney
BACKGROUND: Post-menopausal hypertension has been attributed solely to declining estrogen levels. The purpose of the research is to elucidate the mechanism by which follicle stimulating hormone(FSH) increases renin production involved in the regulation of blood pressure. METHODS: The expression of f...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063271/ https://www.ncbi.nlm.nih.gov/pubmed/35501878 http://dx.doi.org/10.1186/s13098-022-00816-x |
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author | Yu, Zhen Yang, Jing Huang, Wen-Jie Zhang, Tao Li, Xiao-Min Zhao, Wei Li, Xiao-Yong Lu, Yong-Chao |
author_facet | Yu, Zhen Yang, Jing Huang, Wen-Jie Zhang, Tao Li, Xiao-Min Zhao, Wei Li, Xiao-Yong Lu, Yong-Chao |
author_sort | Yu, Zhen |
collection | PubMed |
description | BACKGROUND: Post-menopausal hypertension has been attributed solely to declining estrogen levels. The purpose of the research is to elucidate the mechanism by which follicle stimulating hormone(FSH) increases renin production involved in the regulation of blood pressure. METHODS: The expression of follicle stimulating hormone receptors (FSHRs) in renal juxtaglomerular cells and a As4.1 juxtaglomerular mouse cell line was evaluated. We established a mouse model by ovariectomy (OVX). Ovariectomized mice were treated with gonadotropin-releasing hormone agonist (GnRHa) (OVX + GnRHa). Ovariectomized mice initially received physiological doses of estrogen and were then injected with recombinant FSH (OVX + E + FSH). RESULTS: We found that FSHR was expressed in mouse renal juxtaglomerular cells labeled by renin antibody and in As4.1 cells. FSH promoted renin synthesis via Gsα-coupled FSHRs that activated protein kinase A, cyclic adenosine monophosphate(cAMP) response element-binding protein, extracellular signal-regulated kinase (Erk1/2), Protein kinase B(AKT), and c-Jun N-terminal kinase signaling pathways in As4.1 cells. We found increased serum FSH levels in the ovariectomized mouse with concurrent increases in renin, angiotensin II, heart rate (HR), systolic blood pressure (SBP), diastolic blood pressure (DBP), and mean arterial blood pressure (MAP). Additionally, increases in serum renin, angiotensin II, HR, SBP, DBP, and MAP were reduced by the additional injection of GnRHa. Exogenous FSH administration completely reversed decreases in renin, angiotensin II, HR, SBP, DBP, and MAP even in mice that received physiological doses of estrogen to maintain normal estradiol levels. CONCLUSIONS: Elevated FSH stimulates renin production involving a mechanism that may be relevant to the expression of FSH receptors in renal juxtaglomerular cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-022-00816-x. |
format | Online Article Text |
id | pubmed-9063271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90632712022-05-04 Follicle stimulating hormone promotes production of renin through its receptor in juxtaglomerular cells of kidney Yu, Zhen Yang, Jing Huang, Wen-Jie Zhang, Tao Li, Xiao-Min Zhao, Wei Li, Xiao-Yong Lu, Yong-Chao Diabetol Metab Syndr Research BACKGROUND: Post-menopausal hypertension has been attributed solely to declining estrogen levels. The purpose of the research is to elucidate the mechanism by which follicle stimulating hormone(FSH) increases renin production involved in the regulation of blood pressure. METHODS: The expression of follicle stimulating hormone receptors (FSHRs) in renal juxtaglomerular cells and a As4.1 juxtaglomerular mouse cell line was evaluated. We established a mouse model by ovariectomy (OVX). Ovariectomized mice were treated with gonadotropin-releasing hormone agonist (GnRHa) (OVX + GnRHa). Ovariectomized mice initially received physiological doses of estrogen and were then injected with recombinant FSH (OVX + E + FSH). RESULTS: We found that FSHR was expressed in mouse renal juxtaglomerular cells labeled by renin antibody and in As4.1 cells. FSH promoted renin synthesis via Gsα-coupled FSHRs that activated protein kinase A, cyclic adenosine monophosphate(cAMP) response element-binding protein, extracellular signal-regulated kinase (Erk1/2), Protein kinase B(AKT), and c-Jun N-terminal kinase signaling pathways in As4.1 cells. We found increased serum FSH levels in the ovariectomized mouse with concurrent increases in renin, angiotensin II, heart rate (HR), systolic blood pressure (SBP), diastolic blood pressure (DBP), and mean arterial blood pressure (MAP). Additionally, increases in serum renin, angiotensin II, HR, SBP, DBP, and MAP were reduced by the additional injection of GnRHa. Exogenous FSH administration completely reversed decreases in renin, angiotensin II, HR, SBP, DBP, and MAP even in mice that received physiological doses of estrogen to maintain normal estradiol levels. CONCLUSIONS: Elevated FSH stimulates renin production involving a mechanism that may be relevant to the expression of FSH receptors in renal juxtaglomerular cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-022-00816-x. BioMed Central 2022-05-03 /pmc/articles/PMC9063271/ /pubmed/35501878 http://dx.doi.org/10.1186/s13098-022-00816-x Text en © The Author(s) 2022 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yu, Zhen Yang, Jing Huang, Wen-Jie Zhang, Tao Li, Xiao-Min Zhao, Wei Li, Xiao-Yong Lu, Yong-Chao Follicle stimulating hormone promotes production of renin through its receptor in juxtaglomerular cells of kidney |
title | Follicle stimulating hormone promotes production of renin through its receptor in juxtaglomerular cells of kidney |
title_full | Follicle stimulating hormone promotes production of renin through its receptor in juxtaglomerular cells of kidney |
title_fullStr | Follicle stimulating hormone promotes production of renin through its receptor in juxtaglomerular cells of kidney |
title_full_unstemmed | Follicle stimulating hormone promotes production of renin through its receptor in juxtaglomerular cells of kidney |
title_short | Follicle stimulating hormone promotes production of renin through its receptor in juxtaglomerular cells of kidney |
title_sort | follicle stimulating hormone promotes production of renin through its receptor in juxtaglomerular cells of kidney |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063271/ https://www.ncbi.nlm.nih.gov/pubmed/35501878 http://dx.doi.org/10.1186/s13098-022-00816-x |
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