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

Avicenna J Med Biotechnol

Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran; Research Institute of Animal Embryo Technology, Shahrekord University, Shahrekord, Iran.

Published: August 2016

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 α1 and β1 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 α1 and β1 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 α1 and β1 subunits when Ang II was added during IVC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967548PMC

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