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Stanozolol administration combined with exercise leads to decreased telomerase activity possibly associated with liver aging

Anabolic agents are doping substances which are commonly used in sports. Stanozolol, a 17α-alkylated derivative of testosterone, has a widespread use among athletes and bodybuilders. Several medical and behavioral adverse effects are associated with anabolic androgenic steroids (AAS) abuse, while th...

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Autores principales: Ozcagli, Eren, Kara, Mehtap, Kotil, Tugba, Fragkiadaki, Persefoni, Tzatzarakis, Manolis N., Tsitsimpikou, Christina, Stivaktakis, Polychronis D., Tsoukalas, Dimitrios, Spandidos, Demetrios A., Tsatsakis, Aristides M., Alpertunga, Buket
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979936/
https://www.ncbi.nlm.nih.gov/pubmed/29717770
http://dx.doi.org/10.3892/ijmm.2018.3644
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author Ozcagli, Eren
Kara, Mehtap
Kotil, Tugba
Fragkiadaki, Persefoni
Tzatzarakis, Manolis N.
Tsitsimpikou, Christina
Stivaktakis, Polychronis D.
Tsoukalas, Dimitrios
Spandidos, Demetrios A.
Tsatsakis, Aristides M.
Alpertunga, Buket
author_facet Ozcagli, Eren
Kara, Mehtap
Kotil, Tugba
Fragkiadaki, Persefoni
Tzatzarakis, Manolis N.
Tsitsimpikou, Christina
Stivaktakis, Polychronis D.
Tsoukalas, Dimitrios
Spandidos, Demetrios A.
Tsatsakis, Aristides M.
Alpertunga, Buket
author_sort Ozcagli, Eren
collection PubMed
description Anabolic agents are doping substances which are commonly used in sports. Stanozolol, a 17α-alkylated derivative of testosterone, has a widespread use among athletes and bodybuilders. Several medical and behavioral adverse effects are associated with anabolic androgenic steroids (AAS) abuse, while the liver remains the most well recognized target organ. In the present study, the hepatic effects of stanozolol administration in rats at high doses resembling those used for doping purposes were investigated, in the presence or absence of exercise. Stanozolol and its metabolites, 16-β-hydroxystanozolol and 3′-hydroxystanozolol, were detected in rat livers using liquid chromatography-mass spectrometry (LC-MS). Telomerase activity, which is involved in cellular aging and tumorigenesis, was detected by examining telomerase reverse transcriptase (TERT) and phosphatase and tensin homolog (PTEN) expression levels in the livers of stanozolol-treated rats. Stanozolol induced telomerase activity at the molecular level in the liver tissue of rats and exercise reversed this induction, reflecting possible premature liver tissue aging. PTEN gene expression in the rat livers was practically unaffected either by exercise or by stanozolol administration.
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spelling pubmed-59799362018-06-01 Stanozolol administration combined with exercise leads to decreased telomerase activity possibly associated with liver aging Ozcagli, Eren Kara, Mehtap Kotil, Tugba Fragkiadaki, Persefoni Tzatzarakis, Manolis N. Tsitsimpikou, Christina Stivaktakis, Polychronis D. Tsoukalas, Dimitrios Spandidos, Demetrios A. Tsatsakis, Aristides M. Alpertunga, Buket Int J Mol Med Articles Anabolic agents are doping substances which are commonly used in sports. Stanozolol, a 17α-alkylated derivative of testosterone, has a widespread use among athletes and bodybuilders. Several medical and behavioral adverse effects are associated with anabolic androgenic steroids (AAS) abuse, while the liver remains the most well recognized target organ. In the present study, the hepatic effects of stanozolol administration in rats at high doses resembling those used for doping purposes were investigated, in the presence or absence of exercise. Stanozolol and its metabolites, 16-β-hydroxystanozolol and 3′-hydroxystanozolol, were detected in rat livers using liquid chromatography-mass spectrometry (LC-MS). Telomerase activity, which is involved in cellular aging and tumorigenesis, was detected by examining telomerase reverse transcriptase (TERT) and phosphatase and tensin homolog (PTEN) expression levels in the livers of stanozolol-treated rats. Stanozolol induced telomerase activity at the molecular level in the liver tissue of rats and exercise reversed this induction, reflecting possible premature liver tissue aging. PTEN gene expression in the rat livers was practically unaffected either by exercise or by stanozolol administration. D.A. Spandidos 2018-07 2018-04-26 /pmc/articles/PMC5979936/ /pubmed/29717770 http://dx.doi.org/10.3892/ijmm.2018.3644 Text en Copyright: © Ozcagli et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Ozcagli, Eren
Kara, Mehtap
Kotil, Tugba
Fragkiadaki, Persefoni
Tzatzarakis, Manolis N.
Tsitsimpikou, Christina
Stivaktakis, Polychronis D.
Tsoukalas, Dimitrios
Spandidos, Demetrios A.
Tsatsakis, Aristides M.
Alpertunga, Buket
Stanozolol administration combined with exercise leads to decreased telomerase activity possibly associated with liver aging
title Stanozolol administration combined with exercise leads to decreased telomerase activity possibly associated with liver aging
title_full Stanozolol administration combined with exercise leads to decreased telomerase activity possibly associated with liver aging
title_fullStr Stanozolol administration combined with exercise leads to decreased telomerase activity possibly associated with liver aging
title_full_unstemmed Stanozolol administration combined with exercise leads to decreased telomerase activity possibly associated with liver aging
title_short Stanozolol administration combined with exercise leads to decreased telomerase activity possibly associated with liver aging
title_sort stanozolol administration combined with exercise leads to decreased telomerase activity possibly associated with liver aging
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979936/
https://www.ncbi.nlm.nih.gov/pubmed/29717770
http://dx.doi.org/10.3892/ijmm.2018.3644
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