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Protection against Cyclosporine-Induced Reprotoxicity by Satureja khuzestanica Essential Oil in Male Rats
BACKGROUND: The effects of cyclosporine (Cs), a fungal cyclic polypeptide with potent immunosuppressive activity, on fertility have assumed greater significance with the increasing numbers of transplantations being performed all over the world. Current study was undertaken to investigate the potenti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793177/ https://www.ncbi.nlm.nih.gov/pubmed/26985344 |
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author | Najafi, Gholamreza Farokhi, Farah Shalizar Jalali, Ali Akbarizadeh, Zahra |
author_facet | Najafi, Gholamreza Farokhi, Farah Shalizar Jalali, Ali Akbarizadeh, Zahra |
author_sort | Najafi, Gholamreza |
collection | PubMed |
description | BACKGROUND: The effects of cyclosporine (Cs), a fungal cyclic polypeptide with potent immunosuppressive activity, on fertility have assumed greater significance with the increasing numbers of transplantations being performed all over the world. Current study was undertaken to investigate the potential of Satureja khuzestanica Essential Oil (SEO) as an antioxidant to mitigate Cs-induced reprotoxicity. MATERIALS AND METHODS: In this experimental study (April-July 2012), thirty-two adult male Wistar rats were randomly divided into 4 groups of 8 animals each. Two groups of rats were administered Cs [40 mg/kg/day, per oral (p.o.)] for 45 days. One of these groups received SEO (225 mg/kg/day, p.o.) four hours after Cs administration. A vehicle-treated control group and a SEO control group were also included. Epididymal sperm characteristics, in vitro fertilizing capacity as well as embryo development were evaluated. For statistical analysis, one-way ANOVA and Tukey’s post-hoc test were used, and the value of P<0.05 was considered as the criterion for statistical significance. RESULTS: Sperm count and viability along with fertilization and blastocyst development rates were significantly decreased by Cs treatment. Moreover, Cs-treated group showed significant increases in DNA damage, protamine deficiency of the sperm cells and proportion of spermatozoa with cytoplasmic droplet. Notably, aforementioned parameters were improved to near normal level by SEO co-administration. CONCLUSION: These results suggest that SEO has a protective action against Cs-induced reprotoxicity in a rat model. |
format | Online Article Text |
id | pubmed-4793177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-47931772016-03-16 Protection against Cyclosporine-Induced Reprotoxicity by Satureja khuzestanica Essential Oil in Male Rats Najafi, Gholamreza Farokhi, Farah Shalizar Jalali, Ali Akbarizadeh, Zahra Int J Fertil Steril Original Article BACKGROUND: The effects of cyclosporine (Cs), a fungal cyclic polypeptide with potent immunosuppressive activity, on fertility have assumed greater significance with the increasing numbers of transplantations being performed all over the world. Current study was undertaken to investigate the potential of Satureja khuzestanica Essential Oil (SEO) as an antioxidant to mitigate Cs-induced reprotoxicity. MATERIALS AND METHODS: In this experimental study (April-July 2012), thirty-two adult male Wistar rats were randomly divided into 4 groups of 8 animals each. Two groups of rats were administered Cs [40 mg/kg/day, per oral (p.o.)] for 45 days. One of these groups received SEO (225 mg/kg/day, p.o.) four hours after Cs administration. A vehicle-treated control group and a SEO control group were also included. Epididymal sperm characteristics, in vitro fertilizing capacity as well as embryo development were evaluated. For statistical analysis, one-way ANOVA and Tukey’s post-hoc test were used, and the value of P<0.05 was considered as the criterion for statistical significance. RESULTS: Sperm count and viability along with fertilization and blastocyst development rates were significantly decreased by Cs treatment. Moreover, Cs-treated group showed significant increases in DNA damage, protamine deficiency of the sperm cells and proportion of spermatozoa with cytoplasmic droplet. Notably, aforementioned parameters were improved to near normal level by SEO co-administration. CONCLUSION: These results suggest that SEO has a protective action against Cs-induced reprotoxicity in a rat model. Royan Institute 2016 2015-12-23 /pmc/articles/PMC4793177/ /pubmed/26985344 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Najafi, Gholamreza Farokhi, Farah Shalizar Jalali, Ali Akbarizadeh, Zahra Protection against Cyclosporine-Induced Reprotoxicity by Satureja khuzestanica Essential Oil in Male Rats |
title | Protection against Cyclosporine-Induced Reprotoxicity by
Satureja khuzestanica Essential Oil in Male Rats |
title_full | Protection against Cyclosporine-Induced Reprotoxicity by
Satureja khuzestanica Essential Oil in Male Rats |
title_fullStr | Protection against Cyclosporine-Induced Reprotoxicity by
Satureja khuzestanica Essential Oil in Male Rats |
title_full_unstemmed | Protection against Cyclosporine-Induced Reprotoxicity by
Satureja khuzestanica Essential Oil in Male Rats |
title_short | Protection against Cyclosporine-Induced Reprotoxicity by
Satureja khuzestanica Essential Oil in Male Rats |
title_sort | protection against cyclosporine-induced reprotoxicity by
satureja khuzestanica essential oil in male rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793177/ https://www.ncbi.nlm.nih.gov/pubmed/26985344 |
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