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Comparative study of the protective effects of chicken embryo amniotic fluid, vitamin C and coenzyme Q10 on cyclophosphamide-induced oxidative stress in mice ovaries

Cyclophosphamide is a chemotherapy drug for the treatment of cancer. Chicken embryo amniotic fluid, vitamin C and coenzyme Q10 have anti-oxidant properties. Total of 70 adult female mice were selected and divided into seven groups. The first group that received 2 ml kg(-1) of inactivated amniotic fl...

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Autores principales: Kabirian, Alireza, Batavani, Rooz Ali, Asri-Rezaei, Siamak, Soleimanzadeh, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Urmia University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198161/
https://www.ncbi.nlm.nih.gov/pubmed/30357088
http://dx.doi.org/10.30466/vrf.2018.32085
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author Kabirian, Alireza
Batavani, Rooz Ali
Asri-Rezaei, Siamak
Soleimanzadeh, Ali
author_facet Kabirian, Alireza
Batavani, Rooz Ali
Asri-Rezaei, Siamak
Soleimanzadeh, Ali
author_sort Kabirian, Alireza
collection PubMed
description Cyclophosphamide is a chemotherapy drug for the treatment of cancer. Chicken embryo amniotic fluid, vitamin C and coenzyme Q10 have anti-oxidant properties. Total of 70 adult female mice were selected and divided into seven groups. The first group that received 2 ml kg(-1) of inactivated amniotic fluid subcutaneously. The second group treated with 75 mg kg(-1)of cyclophosphamide by intraperitoneal injection. Third to fifth groups received 1, 2, and 4 ml kg(-1) of chicken embryo amniotic fluid, respectively. The sixth group received vitamin C at a dose of 0.2 mg g(-1) of body weight by oral gavages. Seventh group received 10 mg kg(-1) coenzyme Q10 intraperitoneally. All cyclophosphamide treated groups (3-7) received 75 mg kg(-1) of cyclophosphamide intraperitoneal on day 22. The mice were euthanized on day 29 and ovarian tissue antioxidant enzymes including glutathione peroxidase, superoxide dismutase and catalase activities and malondialdehyde (MDA) were evaluated. Activities of above mentioned enzymes in treatment groups (3-7) was significantly higher than patient control group (2). The results also revealed that MDA levels were higher in the control group in comparison to other treatment groups. Therefore, it is concluded that the chick embryo amniotic fluid and coenzyme Q10 can compete with compounds like vitamin C in increasing the anti-oxidant level in ovarian tissue.
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spelling pubmed-61981612018-10-23 Comparative study of the protective effects of chicken embryo amniotic fluid, vitamin C and coenzyme Q10 on cyclophosphamide-induced oxidative stress in mice ovaries Kabirian, Alireza Batavani, Rooz Ali Asri-Rezaei, Siamak Soleimanzadeh, Ali Vet Res Forum Original Article Cyclophosphamide is a chemotherapy drug for the treatment of cancer. Chicken embryo amniotic fluid, vitamin C and coenzyme Q10 have anti-oxidant properties. Total of 70 adult female mice were selected and divided into seven groups. The first group that received 2 ml kg(-1) of inactivated amniotic fluid subcutaneously. The second group treated with 75 mg kg(-1)of cyclophosphamide by intraperitoneal injection. Third to fifth groups received 1, 2, and 4 ml kg(-1) of chicken embryo amniotic fluid, respectively. The sixth group received vitamin C at a dose of 0.2 mg g(-1) of body weight by oral gavages. Seventh group received 10 mg kg(-1) coenzyme Q10 intraperitoneally. All cyclophosphamide treated groups (3-7) received 75 mg kg(-1) of cyclophosphamide intraperitoneal on day 22. The mice were euthanized on day 29 and ovarian tissue antioxidant enzymes including glutathione peroxidase, superoxide dismutase and catalase activities and malondialdehyde (MDA) were evaluated. Activities of above mentioned enzymes in treatment groups (3-7) was significantly higher than patient control group (2). The results also revealed that MDA levels were higher in the control group in comparison to other treatment groups. Therefore, it is concluded that the chick embryo amniotic fluid and coenzyme Q10 can compete with compounds like vitamin C in increasing the anti-oxidant level in ovarian tissue. Urmia University Press 2018 2018-09-15 /pmc/articles/PMC6198161/ /pubmed/30357088 http://dx.doi.org/10.30466/vrf.2018.32085 Text en © 2018 Urmia University. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-noncommercial 4.0 International License, (https://creativecommons.org/licenses/by-nc/4.0/) which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Kabirian, Alireza
Batavani, Rooz Ali
Asri-Rezaei, Siamak
Soleimanzadeh, Ali
Comparative study of the protective effects of chicken embryo amniotic fluid, vitamin C and coenzyme Q10 on cyclophosphamide-induced oxidative stress in mice ovaries
title Comparative study of the protective effects of chicken embryo amniotic fluid, vitamin C and coenzyme Q10 on cyclophosphamide-induced oxidative stress in mice ovaries
title_full Comparative study of the protective effects of chicken embryo amniotic fluid, vitamin C and coenzyme Q10 on cyclophosphamide-induced oxidative stress in mice ovaries
title_fullStr Comparative study of the protective effects of chicken embryo amniotic fluid, vitamin C and coenzyme Q10 on cyclophosphamide-induced oxidative stress in mice ovaries
title_full_unstemmed Comparative study of the protective effects of chicken embryo amniotic fluid, vitamin C and coenzyme Q10 on cyclophosphamide-induced oxidative stress in mice ovaries
title_short Comparative study of the protective effects of chicken embryo amniotic fluid, vitamin C and coenzyme Q10 on cyclophosphamide-induced oxidative stress in mice ovaries
title_sort comparative study of the protective effects of chicken embryo amniotic fluid, vitamin c and coenzyme q10 on cyclophosphamide-induced oxidative stress in mice ovaries
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198161/
https://www.ncbi.nlm.nih.gov/pubmed/30357088
http://dx.doi.org/10.30466/vrf.2018.32085
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