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Short-term levosimendan treatment protects rat testes against oxidative stress

The objective of this study was to evaluate the effect of short-term levosimendan exposure on oxidant/antioxidant status and trace element levels in the testes of rats under physiological conditions. Twenty male Wistar albino rats were randomly divided into two groups of 10 animals each. Group 1 was...

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Autores principales: Yuksel, M.B., Kavak, S., Gecit, I., Basel, H., Gümrükçüoğlu, H.A., Demir, H., Meral, İ.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Medicina Tropical 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854241/
https://www.ncbi.nlm.nih.gov/pubmed/22584643
http://dx.doi.org/10.1590/S0100-879X2012007500075
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author Yuksel, M.B.
Kavak, S.
Gecit, I.
Basel, H.
Gümrükçüoğlu, H.A.
Demir, H.
Meral, İ.
author_facet Yuksel, M.B.
Kavak, S.
Gecit, I.
Basel, H.
Gümrükçüoğlu, H.A.
Demir, H.
Meral, İ.
author_sort Yuksel, M.B.
collection PubMed
description The objective of this study was to evaluate the effect of short-term levosimendan exposure on oxidant/antioxidant status and trace element levels in the testes of rats under physiological conditions. Twenty male Wistar albino rats were randomly divided into two groups of 10 animals each. Group 1 was not exposed to levosimendan and served as control. Levosimendan (12 µg/kg) diluted in 10 mL 0.9% NaCl was administered intraperitoneally to group 2. Animals of both groups were sacrificed after 3 days and their testes were harvested for the determination of changes in tissue oxidant/antioxidant status and trace element levels. Tissue malondialdehyde (MDA) was significantly lower in the levosimendan group (P < 0.001) than in the untreated control group and superoxide dismutase and glutathione peroxidase (GSH-Px) levels were significantly higher in the levosimendan group (P < 0.001). Carbonic anhydrase, catalase and GSH levels were not significantly different from controls. Mg and Zn levels of testes were significantly higher (P < 0.001) and Co, Pb, Cd, Mn, and Cu were significantly lower (P < 0.001) in group 2 compared to group 1. Fe levels were similar for the two groups (P = 0.94). These results suggest that 3-day exposure to levosimendan induced a significant decrease in tissue MDA level, which is a lipid peroxidation product and an indicator of oxidative stress, and a significant increase in the activity of an important number of the enzymes that protect against oxidative stress in rat testes.
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spelling pubmed-38542412013-12-16 Short-term levosimendan treatment protects rat testes against oxidative stress Yuksel, M.B. Kavak, S. Gecit, I. Basel, H. Gümrükçüoğlu, H.A. Demir, H. Meral, İ. Braz J Med Biol Res Short Communication The objective of this study was to evaluate the effect of short-term levosimendan exposure on oxidant/antioxidant status and trace element levels in the testes of rats under physiological conditions. Twenty male Wistar albino rats were randomly divided into two groups of 10 animals each. Group 1 was not exposed to levosimendan and served as control. Levosimendan (12 µg/kg) diluted in 10 mL 0.9% NaCl was administered intraperitoneally to group 2. Animals of both groups were sacrificed after 3 days and their testes were harvested for the determination of changes in tissue oxidant/antioxidant status and trace element levels. Tissue malondialdehyde (MDA) was significantly lower in the levosimendan group (P < 0.001) than in the untreated control group and superoxide dismutase and glutathione peroxidase (GSH-Px) levels were significantly higher in the levosimendan group (P < 0.001). Carbonic anhydrase, catalase and GSH levels were not significantly different from controls. Mg and Zn levels of testes were significantly higher (P < 0.001) and Co, Pb, Cd, Mn, and Cu were significantly lower (P < 0.001) in group 2 compared to group 1. Fe levels were similar for the two groups (P = 0.94). These results suggest that 3-day exposure to levosimendan induced a significant decrease in tissue MDA level, which is a lipid peroxidation product and an indicator of oxidative stress, and a significant increase in the activity of an important number of the enzymes that protect against oxidative stress in rat testes. Sociedade Brasileira de Medicina Tropical 2012-05-18 /pmc/articles/PMC3854241/ /pubmed/22584643 http://dx.doi.org/10.1590/S0100-879X2012007500075 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Yuksel, M.B.
Kavak, S.
Gecit, I.
Basel, H.
Gümrükçüoğlu, H.A.
Demir, H.
Meral, İ.
Short-term levosimendan treatment protects rat testes against oxidative stress
title Short-term levosimendan treatment protects rat testes against oxidative stress
title_full Short-term levosimendan treatment protects rat testes against oxidative stress
title_fullStr Short-term levosimendan treatment protects rat testes against oxidative stress
title_full_unstemmed Short-term levosimendan treatment protects rat testes against oxidative stress
title_short Short-term levosimendan treatment protects rat testes against oxidative stress
title_sort short-term levosimendan treatment protects rat testes against oxidative stress
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854241/
https://www.ncbi.nlm.nih.gov/pubmed/22584643
http://dx.doi.org/10.1590/S0100-879X2012007500075
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