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The Effect of Media Supplementation with Angiotensin on Developmental Competence of Ovine Embryos Derived from Vitrified-warmed Oocytes

BACKGROUND: This study was aimed to assess the effects of angiotensin II (Ang II) supplementation to the In Vitro Maturation (IVM) and In Vitro Culture (IVC) media of vitrified-warmed ovine oocytes on their developmental competence and expression of Na(+)/K(+)/ATPase in resulting embryos. METHODS: T...

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Autores principales: Naderi, Mohammad Mehdi, Borjian Boroujeni, Sara, Sarvari, Ali, Heidari, Banafsheh, Akhondi, Mohammad Mehdi, Zarnani, Amir-Hassan, Shirazi, Abolfazl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Research Institute 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967548/
https://www.ncbi.nlm.nih.gov/pubmed/27563427
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author Naderi, Mohammad Mehdi
Borjian Boroujeni, Sara
Sarvari, Ali
Heidari, Banafsheh
Akhondi, Mohammad Mehdi
Zarnani, Amir-Hassan
Shirazi, Abolfazl
author_facet Naderi, Mohammad Mehdi
Borjian Boroujeni, Sara
Sarvari, Ali
Heidari, Banafsheh
Akhondi, Mohammad Mehdi
Zarnani, Amir-Hassan
Shirazi, Abolfazl
author_sort Naderi, Mohammad Mehdi
collection PubMed
description BACKGROUND: This study was aimed to assess the effects of angiotensin II (Ang II) supplementation to the In Vitro Maturation (IVM) and In Vitro Culture (IVC) media of vitrified-warmed ovine oocytes on their developmental competence and expression of Na(+)/K(+)/ATPase in resulting embryos. METHODS: The slaughterhouse-derived immature oocytes (n=1069) were randomly distributed into four experimental groups: groups I and II) IVM/IVF and IVC of fresh and vitrified oocytes without angiotensin supplementation (Control-Fresh and Control-Vit groups, respectively); group III) IVM of vitrified oocytes in the presence of Ang II followed by IVF/IVC (Vit-IVM group); and group IV) IVM/IVF of vitrified oocytes followed by IVC wherein the embryos were exposed to Ang II on day 4 of IVC (Vit-D4 group). The embryos were immunostained with primary antibodies against Na(+)/K(+)/ATPase α(1) and β(1) subunits. RESULTS: In Vit-IVM and Vit-D4 groups, the rates of expanded and total blastocysts on day 7 as well as the proportion of blastocysts on day 8 were increased. The expression of Na(+)/K(+)/ATPase α(1) and β(1) subunits were positively influenced by the addition of Ang II on day 4 (Vit-D4 group). CONCLUSION: The addition of Ang II to the IVM and IVC media could improve blastocysts formation in vitrified sheep oocytes. This improvement might be related to the greater expression of Na(+)/K(+)/ATPase α(1) and β(1) subunits when Ang II was added during IVC.
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spelling pubmed-49675482016-08-25 The Effect of Media Supplementation with Angiotensin on Developmental Competence of Ovine Embryos Derived from Vitrified-warmed Oocytes Naderi, Mohammad Mehdi Borjian Boroujeni, Sara Sarvari, Ali Heidari, Banafsheh Akhondi, Mohammad Mehdi Zarnani, Amir-Hassan Shirazi, Abolfazl Avicenna J Med Biotechnol Original Article BACKGROUND: This study was aimed to assess the effects of angiotensin II (Ang II) supplementation to the In Vitro Maturation (IVM) and In Vitro Culture (IVC) media of vitrified-warmed ovine oocytes on their developmental competence and expression of Na(+)/K(+)/ATPase in resulting embryos. METHODS: The slaughterhouse-derived immature oocytes (n=1069) were randomly distributed into four experimental groups: groups I and II) IVM/IVF and IVC of fresh and vitrified oocytes without angiotensin supplementation (Control-Fresh and Control-Vit groups, respectively); group III) IVM of vitrified oocytes in the presence of Ang II followed by IVF/IVC (Vit-IVM group); and group IV) IVM/IVF of vitrified oocytes followed by IVC wherein the embryos were exposed to Ang II on day 4 of IVC (Vit-D4 group). The embryos were immunostained with primary antibodies against Na(+)/K(+)/ATPase α(1) and β(1) subunits. RESULTS: In Vit-IVM and Vit-D4 groups, the rates of expanded and total blastocysts on day 7 as well as the proportion of blastocysts on day 8 were increased. The expression of Na(+)/K(+)/ATPase α(1) and β(1) subunits were positively influenced by the addition of Ang II on day 4 (Vit-D4 group). CONCLUSION: The addition of Ang II to the IVM and IVC media could improve blastocysts formation in vitrified sheep oocytes. This improvement might be related to the greater expression of Na(+)/K(+)/ATPase α(1) and β(1) subunits when Ang II was added during IVC. Avicenna Research Institute 2016 /pmc/articles/PMC4967548/ /pubmed/27563427 Text en Copyright© 2016 Avicenna Research Institute This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License 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
Naderi, Mohammad Mehdi
Borjian Boroujeni, Sara
Sarvari, Ali
Heidari, Banafsheh
Akhondi, Mohammad Mehdi
Zarnani, Amir-Hassan
Shirazi, Abolfazl
The Effect of Media Supplementation with Angiotensin on Developmental Competence of Ovine Embryos Derived from Vitrified-warmed Oocytes
title The Effect of Media Supplementation with Angiotensin on Developmental Competence of Ovine Embryos Derived from Vitrified-warmed Oocytes
title_full The Effect of Media Supplementation with Angiotensin on Developmental Competence of Ovine Embryos Derived from Vitrified-warmed Oocytes
title_fullStr The Effect of Media Supplementation with Angiotensin on Developmental Competence of Ovine Embryos Derived from Vitrified-warmed Oocytes
title_full_unstemmed The Effect of Media Supplementation with Angiotensin on Developmental Competence of Ovine Embryos Derived from Vitrified-warmed Oocytes
title_short The Effect of Media Supplementation with Angiotensin on Developmental Competence of Ovine Embryos Derived from Vitrified-warmed Oocytes
title_sort effect of media supplementation with angiotensin on developmental competence of ovine embryos derived from vitrified-warmed oocytes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967548/
https://www.ncbi.nlm.nih.gov/pubmed/27563427
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