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The impact of Anastrazole and Letrozole on the metabolic profile in an experimental animal model
Anastrazole and Letrozole are used as endocrine therapy for breast cancer patients. Previous studies suggested a possible association with metabolic and liver adverse effects. Their results are conflicting. Fifty-five 4-week-old female Wistar rats were allocated in 4 groups 1) ovariectomy control (O...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664924/ https://www.ncbi.nlm.nih.gov/pubmed/26620133 http://dx.doi.org/10.1038/srep17493 |
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author | Boutas, Ioannis Pergialiotis, Vasilios Salakos, Nicolaos Agrogiannis, George Konstantopoulos, Panagiotis Korou, Laskarina-Maria Kalampokas, Theodoros Gregoriou, Odysseas Creatsas, George Perrea, Despina |
author_facet | Boutas, Ioannis Pergialiotis, Vasilios Salakos, Nicolaos Agrogiannis, George Konstantopoulos, Panagiotis Korou, Laskarina-Maria Kalampokas, Theodoros Gregoriou, Odysseas Creatsas, George Perrea, Despina |
author_sort | Boutas, Ioannis |
collection | PubMed |
description | Anastrazole and Letrozole are used as endocrine therapy for breast cancer patients. Previous studies suggested a possible association with metabolic and liver adverse effects. Their results are conflicting. Fifty-five 4-week-old female Wistar rats were allocated in 4 groups 1) ovariectomy control (OC), 2) ovariectomy-Anastrazole (OA) 3) ovariectomy -Letrozole (OL), 4) control. Serum glucose, cholesterol, triglycerides, HDL-c and LDL-c were measured at baseline, 2 and 4 months. At the end, the animals‘ liver were dissected for pathology. At 4 months, total cholesterol differed among the OC and OL groups (p = 0.15) and the control and OL groups (p = 0.12). LDL-C differed between the control and OC groups (p = 0.015) as well as between the control and OA (p =0 .015) and OL groups (p = 0.002). OC group triglycerides, differed from those of the OL group (p =0 .002) and the control group (p = 0.007). The OA also significantly differed from the OL (p = 0.50). Liver pathology analysis revealed differences among groups with favored mild steatosis and ballooning. Anastrazole and Letrozole seem to negatively influence the lipid profile in our experimental model. This information should be taken in caution by medical oncologists when addressing patients with altered lipid metabolism. |
format | Online Article Text |
id | pubmed-4664924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46649242015-12-03 The impact of Anastrazole and Letrozole on the metabolic profile in an experimental animal model Boutas, Ioannis Pergialiotis, Vasilios Salakos, Nicolaos Agrogiannis, George Konstantopoulos, Panagiotis Korou, Laskarina-Maria Kalampokas, Theodoros Gregoriou, Odysseas Creatsas, George Perrea, Despina Sci Rep Article Anastrazole and Letrozole are used as endocrine therapy for breast cancer patients. Previous studies suggested a possible association with metabolic and liver adverse effects. Their results are conflicting. Fifty-five 4-week-old female Wistar rats were allocated in 4 groups 1) ovariectomy control (OC), 2) ovariectomy-Anastrazole (OA) 3) ovariectomy -Letrozole (OL), 4) control. Serum glucose, cholesterol, triglycerides, HDL-c and LDL-c were measured at baseline, 2 and 4 months. At the end, the animals‘ liver were dissected for pathology. At 4 months, total cholesterol differed among the OC and OL groups (p = 0.15) and the control and OL groups (p = 0.12). LDL-C differed between the control and OC groups (p = 0.015) as well as between the control and OA (p =0 .015) and OL groups (p = 0.002). OC group triglycerides, differed from those of the OL group (p =0 .002) and the control group (p = 0.007). The OA also significantly differed from the OL (p = 0.50). Liver pathology analysis revealed differences among groups with favored mild steatosis and ballooning. Anastrazole and Letrozole seem to negatively influence the lipid profile in our experimental model. This information should be taken in caution by medical oncologists when addressing patients with altered lipid metabolism. Nature Publishing Group 2015-12-01 /pmc/articles/PMC4664924/ /pubmed/26620133 http://dx.doi.org/10.1038/srep17493 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Boutas, Ioannis Pergialiotis, Vasilios Salakos, Nicolaos Agrogiannis, George Konstantopoulos, Panagiotis Korou, Laskarina-Maria Kalampokas, Theodoros Gregoriou, Odysseas Creatsas, George Perrea, Despina The impact of Anastrazole and Letrozole on the metabolic profile in an experimental animal model |
title | The impact of Anastrazole and Letrozole on the metabolic profile in an experimental animal model |
title_full | The impact of Anastrazole and Letrozole on the metabolic profile in an experimental animal model |
title_fullStr | The impact of Anastrazole and Letrozole on the metabolic profile in an experimental animal model |
title_full_unstemmed | The impact of Anastrazole and Letrozole on the metabolic profile in an experimental animal model |
title_short | The impact of Anastrazole and Letrozole on the metabolic profile in an experimental animal model |
title_sort | impact of anastrazole and letrozole on the metabolic profile in an experimental animal model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664924/ https://www.ncbi.nlm.nih.gov/pubmed/26620133 http://dx.doi.org/10.1038/srep17493 |
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