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Effect of Cross-Sex Hormonal Replacement on Antioxidant Enzymes in Rat Retroperitoneal Fat Adipocytes
We report the effect of cross-sex hormonal replacement on antioxidant enzymes from rat retroperitoneal fat adipocytes. Eight rats of each gender were assigned to each of the following groups: control groups were intact female or male (F and M, resp.). Experimental groups were ovariectomized F (OvxF)...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007368/ https://www.ncbi.nlm.nih.gov/pubmed/27630756 http://dx.doi.org/10.1155/2016/1527873 |
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author | Pérez-Torres, Israel Guarner-Lans, Verónica Zúñiga-Muñoz, Alejandra Velázquez Espejel, Rodrigo Cabrera-Orefice, Alfredo Uribe-Carvajal, Salvador Pavón, Natalia |
author_facet | Pérez-Torres, Israel Guarner-Lans, Verónica Zúñiga-Muñoz, Alejandra Velázquez Espejel, Rodrigo Cabrera-Orefice, Alfredo Uribe-Carvajal, Salvador Pavón, Natalia |
author_sort | Pérez-Torres, Israel |
collection | PubMed |
description | We report the effect of cross-sex hormonal replacement on antioxidant enzymes from rat retroperitoneal fat adipocytes. Eight rats of each gender were assigned to each of the following groups: control groups were intact female or male (F and M, resp.). Experimental groups were ovariectomized F (OvxF), castrated M (CasM), OvxF plus testosterone (OvxF + T), and CasM plus estradiol (CasM + E(2)) groups. After sacrifice, retroperitoneal fat was dissected and processed for histology. Adipocytes were isolated and the following enzymatic activities were determined: Cu-Zn superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione-S-transferase (GST), and glutathione reductase (GR). Also, glutathione (GSH) and lipid peroxidation (LPO) were measured. In OvxF, retroperitoneal fat increased and adipocytes were enlarged, while in CasM rats a decrease in retroperitoneal fat and small adipocytes are observed. The cross-sex hormonal replacement in F rats was associated with larger adipocytes and a further decreased activity of Cu-Zn SOD, CAT, GPx, GST, GR, and GSH, in addition to an increase in LPO. CasM + E(2) exhibited the opposite effects showing further activation antioxidant enzymes and decreases in LPO. In conclusion, E(2) deficiency favors an increase in retroperitoneal fat and large adipocytes. Cross-sex hormonal replacement in F rats aggravates the condition by inhibiting antioxidant enzymes. |
format | Online Article Text |
id | pubmed-5007368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-50073682016-09-14 Effect of Cross-Sex Hormonal Replacement on Antioxidant Enzymes in Rat Retroperitoneal Fat Adipocytes Pérez-Torres, Israel Guarner-Lans, Verónica Zúñiga-Muñoz, Alejandra Velázquez Espejel, Rodrigo Cabrera-Orefice, Alfredo Uribe-Carvajal, Salvador Pavón, Natalia Oxid Med Cell Longev Research Article We report the effect of cross-sex hormonal replacement on antioxidant enzymes from rat retroperitoneal fat adipocytes. Eight rats of each gender were assigned to each of the following groups: control groups were intact female or male (F and M, resp.). Experimental groups were ovariectomized F (OvxF), castrated M (CasM), OvxF plus testosterone (OvxF + T), and CasM plus estradiol (CasM + E(2)) groups. After sacrifice, retroperitoneal fat was dissected and processed for histology. Adipocytes were isolated and the following enzymatic activities were determined: Cu-Zn superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione-S-transferase (GST), and glutathione reductase (GR). Also, glutathione (GSH) and lipid peroxidation (LPO) were measured. In OvxF, retroperitoneal fat increased and adipocytes were enlarged, while in CasM rats a decrease in retroperitoneal fat and small adipocytes are observed. The cross-sex hormonal replacement in F rats was associated with larger adipocytes and a further decreased activity of Cu-Zn SOD, CAT, GPx, GST, GR, and GSH, in addition to an increase in LPO. CasM + E(2) exhibited the opposite effects showing further activation antioxidant enzymes and decreases in LPO. In conclusion, E(2) deficiency favors an increase in retroperitoneal fat and large adipocytes. Cross-sex hormonal replacement in F rats aggravates the condition by inhibiting antioxidant enzymes. Hindawi Publishing Corporation 2016 2016-08-18 /pmc/articles/PMC5007368/ /pubmed/27630756 http://dx.doi.org/10.1155/2016/1527873 Text en Copyright © 2016 Israel Pérez-Torres et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Pérez-Torres, Israel Guarner-Lans, Verónica Zúñiga-Muñoz, Alejandra Velázquez Espejel, Rodrigo Cabrera-Orefice, Alfredo Uribe-Carvajal, Salvador Pavón, Natalia Effect of Cross-Sex Hormonal Replacement on Antioxidant Enzymes in Rat Retroperitoneal Fat Adipocytes |
title | Effect of Cross-Sex Hormonal Replacement on Antioxidant Enzymes in Rat Retroperitoneal Fat Adipocytes |
title_full | Effect of Cross-Sex Hormonal Replacement on Antioxidant Enzymes in Rat Retroperitoneal Fat Adipocytes |
title_fullStr | Effect of Cross-Sex Hormonal Replacement on Antioxidant Enzymes in Rat Retroperitoneal Fat Adipocytes |
title_full_unstemmed | Effect of Cross-Sex Hormonal Replacement on Antioxidant Enzymes in Rat Retroperitoneal Fat Adipocytes |
title_short | Effect of Cross-Sex Hormonal Replacement on Antioxidant Enzymes in Rat Retroperitoneal Fat Adipocytes |
title_sort | effect of cross-sex hormonal replacement on antioxidant enzymes in rat retroperitoneal fat adipocytes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007368/ https://www.ncbi.nlm.nih.gov/pubmed/27630756 http://dx.doi.org/10.1155/2016/1527873 |
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