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Protective effect of ethyl pyruvate on mice sperm parameters in phenylhydrazine induced hemolytic anemia
The aim of the present study was to assess the protective effect of ethyl pyruvate (EP) on sperm quality parameters, testosterone level and malondialdehyde (MDA) in phenylhydrazine (PHZ) treated mice. For this purpose, 32 NMRI mice with the age range of 8 to 10 weeks, weight average 26.0 ± 2.0 g, we...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Urmia University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867039/ https://www.ncbi.nlm.nih.gov/pubmed/27226889 |
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author | Mozafari, Ali Akbar Shahrooz, Rasoul Ahmadi, Abbas Malekinjad, Hassan Mardani, Karim |
author_facet | Mozafari, Ali Akbar Shahrooz, Rasoul Ahmadi, Abbas Malekinjad, Hassan Mardani, Karim |
author_sort | Mozafari, Ali Akbar |
collection | PubMed |
description | The aim of the present study was to assess the protective effect of ethyl pyruvate (EP) on sperm quality parameters, testosterone level and malondialdehyde (MDA) in phenylhydrazine (PHZ) treated mice. For this purpose, 32 NMRI mice with the age range of 8 to 10 weeks, weight average 26.0 ± 2.0 g, were randomly divided into four equal groups. The control group (1) received normal saline (0. 1 mL per day) by intraperitoneal injection (IP). Group 2 (PHZ group) was treated with initial dose of PHZ (8 mg 100 g(-1), IP) followed by 6 mg 100 g(-1) , IP every 48 hr. Group 3, (Group PHZ+EP) received PHZ (according to the previous prescription) with EP (40 mg kg(-1), daily, IP). Ethyl pyruvate group (4) received only EP (40 mg kg(-1), daily, IP). Treatment period was 35 days. After euthanasia, sperms from caudal region of epididymis were collected and the total mean sperm count, sperm viability, motility and morphology were determined. Testis tissue MDA and serum testosterone levels of all experimental groups were also evaluated. A considerable reduction in mean percentage of number, natural morphology of sperm, sperm motility and viability and serum testosterone concentration besides DNA injury increment among mice treating with PHZ in comparison with control group were observed. However, in PHZ+EP group the above mentioned parameters were improved. This study showed that PHZ caused induction of toxicity on sperm parameters and reduction of testosterone as well as the increment of MDA level and EP as an antioxidant could reduce destructive effects of PHZ on sperm parameters, testosterone level and lipid peroxidation. |
format | Online Article Text |
id | pubmed-4867039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Urmia University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48670392016-05-25 Protective effect of ethyl pyruvate on mice sperm parameters in phenylhydrazine induced hemolytic anemia Mozafari, Ali Akbar Shahrooz, Rasoul Ahmadi, Abbas Malekinjad, Hassan Mardani, Karim Vet Res Forum Original Article The aim of the present study was to assess the protective effect of ethyl pyruvate (EP) on sperm quality parameters, testosterone level and malondialdehyde (MDA) in phenylhydrazine (PHZ) treated mice. For this purpose, 32 NMRI mice with the age range of 8 to 10 weeks, weight average 26.0 ± 2.0 g, were randomly divided into four equal groups. The control group (1) received normal saline (0. 1 mL per day) by intraperitoneal injection (IP). Group 2 (PHZ group) was treated with initial dose of PHZ (8 mg 100 g(-1), IP) followed by 6 mg 100 g(-1) , IP every 48 hr. Group 3, (Group PHZ+EP) received PHZ (according to the previous prescription) with EP (40 mg kg(-1), daily, IP). Ethyl pyruvate group (4) received only EP (40 mg kg(-1), daily, IP). Treatment period was 35 days. After euthanasia, sperms from caudal region of epididymis were collected and the total mean sperm count, sperm viability, motility and morphology were determined. Testis tissue MDA and serum testosterone levels of all experimental groups were also evaluated. A considerable reduction in mean percentage of number, natural morphology of sperm, sperm motility and viability and serum testosterone concentration besides DNA injury increment among mice treating with PHZ in comparison with control group were observed. However, in PHZ+EP group the above mentioned parameters were improved. This study showed that PHZ caused induction of toxicity on sperm parameters and reduction of testosterone as well as the increment of MDA level and EP as an antioxidant could reduce destructive effects of PHZ on sperm parameters, testosterone level and lipid peroxidation. Urmia University Press 2016 2016-03-15 /pmc/articles/PMC4867039/ /pubmed/27226889 Text en © 2016 Urmia University. All rights reserved. This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Mozafari, Ali Akbar Shahrooz, Rasoul Ahmadi, Abbas Malekinjad, Hassan Mardani, Karim Protective effect of ethyl pyruvate on mice sperm parameters in phenylhydrazine induced hemolytic anemia |
title | Protective effect of ethyl pyruvate on mice sperm parameters in phenylhydrazine induced hemolytic anemia |
title_full | Protective effect of ethyl pyruvate on mice sperm parameters in phenylhydrazine induced hemolytic anemia |
title_fullStr | Protective effect of ethyl pyruvate on mice sperm parameters in phenylhydrazine induced hemolytic anemia |
title_full_unstemmed | Protective effect of ethyl pyruvate on mice sperm parameters in phenylhydrazine induced hemolytic anemia |
title_short | Protective effect of ethyl pyruvate on mice sperm parameters in phenylhydrazine induced hemolytic anemia |
title_sort | protective effect of ethyl pyruvate on mice sperm parameters in phenylhydrazine induced hemolytic anemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867039/ https://www.ncbi.nlm.nih.gov/pubmed/27226889 |
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