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In vitro maturation of Mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions

OBJECTIVE: To evaluate in vitro oocyte maturation rates in embryonic culture medium after induction by hyperosmotic shock caused by exposure to vitrification solutions. METHODS: Bilateral oophorectomy was performed on 20 prepubescent female mice (Swiss). Immature (Prophase I) oocytes (N = 400) were...

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Autores principales: Koaski, Erica, Colle, Cláudia Schneider, Salvador, Rafael Alonso, Amaral, Vera Lucia Lângaro, Senn, Alfred Paul, Til, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brazilian Society of Assisted Reproduction 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8083860/
https://www.ncbi.nlm.nih.gov/pubmed/33565296
http://dx.doi.org/10.5935/1518-0557.20200084
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author Koaski, Erica
Colle, Cláudia Schneider
Salvador, Rafael Alonso
Amaral, Vera Lucia Lângaro
Senn, Alfred Paul
Til, David
author_facet Koaski, Erica
Colle, Cláudia Schneider
Salvador, Rafael Alonso
Amaral, Vera Lucia Lângaro
Senn, Alfred Paul
Til, David
author_sort Koaski, Erica
collection PubMed
description OBJECTIVE: To evaluate in vitro oocyte maturation rates in embryonic culture medium after induction by hyperosmotic shock caused by exposure to vitrification solutions. METHODS: Bilateral oophorectomy was performed on 20 prepubescent female mice (Swiss). Immature (Prophase I) oocytes (N = 400) were obtained by ovarian dissection, divided into 4 groups, and transferred to culture dishes containing fertilization medium (Sydney IVF Fertilization Medium, Cook(®) Medical). The control group (CG) did not receive treatment, the test groups (G1, G2, G3) were treated with vitrification solution - 2 (VI-2: 14 M sucrose + ethylene glycol and dimethyl sulfoxide) for 30 seconds and subsequently: G1: 30 seconds in devitrification solution - 2 (DV-2: 0.5M sucrose); G2: 60 seconds DV-2; G3: 60 seconds DV-1(1M sucrose) and 180 seconds DV-2. All groups were cultivated for 24 hours in an incubator at 37ºC and 5% CO2 (Thermo model 3110). After this period, we checked their maturation status. RESULTS: Oocytes exposed to VI-2, DV-1 and DV-2 (G3) showed the highest rate of competence in resuming meiosis and reaching the MII stage; however, there was no statistically significant difference (G3 = 50.5% - 49/97; CG = 27.8% - 10/30). CONCLUSIONS: Oocyte exposure to vitrification solutions, in order to cause osmotic shock, did not interfere with the resumption of meiosis in mice oocytes.
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spelling pubmed-80838602021-05-05 In vitro maturation of Mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions Koaski, Erica Colle, Cláudia Schneider Salvador, Rafael Alonso Amaral, Vera Lucia Lângaro Senn, Alfred Paul Til, David JBRA Assist Reprod Original Article OBJECTIVE: To evaluate in vitro oocyte maturation rates in embryonic culture medium after induction by hyperosmotic shock caused by exposure to vitrification solutions. METHODS: Bilateral oophorectomy was performed on 20 prepubescent female mice (Swiss). Immature (Prophase I) oocytes (N = 400) were obtained by ovarian dissection, divided into 4 groups, and transferred to culture dishes containing fertilization medium (Sydney IVF Fertilization Medium, Cook(®) Medical). The control group (CG) did not receive treatment, the test groups (G1, G2, G3) were treated with vitrification solution - 2 (VI-2: 14 M sucrose + ethylene glycol and dimethyl sulfoxide) for 30 seconds and subsequently: G1: 30 seconds in devitrification solution - 2 (DV-2: 0.5M sucrose); G2: 60 seconds DV-2; G3: 60 seconds DV-1(1M sucrose) and 180 seconds DV-2. All groups were cultivated for 24 hours in an incubator at 37ºC and 5% CO2 (Thermo model 3110). After this period, we checked their maturation status. RESULTS: Oocytes exposed to VI-2, DV-1 and DV-2 (G3) showed the highest rate of competence in resuming meiosis and reaching the MII stage; however, there was no statistically significant difference (G3 = 50.5% - 49/97; CG = 27.8% - 10/30). CONCLUSIONS: Oocyte exposure to vitrification solutions, in order to cause osmotic shock, did not interfere with the resumption of meiosis in mice oocytes. Brazilian Society of Assisted Reproduction 2021 /pmc/articles/PMC8083860/ /pubmed/33565296 http://dx.doi.org/10.5935/1518-0557.20200084 Text en https://creativecommons.org/licenses/by/4.0/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
Koaski, Erica
Colle, Cláudia Schneider
Salvador, Rafael Alonso
Amaral, Vera Lucia Lângaro
Senn, Alfred Paul
Til, David
In vitro maturation of Mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions
title In vitro maturation of Mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions
title_full In vitro maturation of Mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions
title_fullStr In vitro maturation of Mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions
title_full_unstemmed In vitro maturation of Mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions
title_short In vitro maturation of Mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions
title_sort in vitro maturation of mus musculus mice oocytes after hyperosmotic shock induced by vitrification solutions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8083860/
https://www.ncbi.nlm.nih.gov/pubmed/33565296
http://dx.doi.org/10.5935/1518-0557.20200084
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