Superovulation Does Not Alter Calcium Oscillations Following Fertilization

Superovulation is a common approach to maximize the number of eggs available for either clinical assisted reproductive technologies or experimental animal studies. This procedure provides supraphysiological amounts of gonadotropins to promote continued growth and maturation of ovarian follicles that...

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Autores principales: Virginia Savy, Paula Stein, Min Shi, Carmen J. Williams
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Lenguaje:EN
Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://doaj.org/article/f48dc4fad44143398b076c1ae1356685
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spelling oai:doaj.org-article:f48dc4fad44143398b076c1ae13566852021-11-04T05:18:18ZSuperovulation Does Not Alter Calcium Oscillations Following Fertilization2296-634X10.3389/fcell.2021.762057https://doaj.org/article/f48dc4fad44143398b076c1ae13566852021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fcell.2021.762057/fullhttps://doaj.org/toc/2296-634XSuperovulation is a common approach to maximize the number of eggs available for either clinical assisted reproductive technologies or experimental animal studies. This procedure provides supraphysiological amounts of gonadotropins to promote continued growth and maturation of ovarian follicles that otherwise would undergo atresia. There is evidence in mice, cows, sheep, and humans that superovulation has a detrimental impact on the quality of the resulting ovulated eggs or embryos. Here we tested the hypothesis that eggs derived from superovulation have a reduced capacity to support calcium oscillations, which are a critical factor in the success of embryo development. Eggs were obtained from mice that were either naturally cycling or underwent a standard superovulation protocol. The eggs were either parthenogenetically activated using strontium or fertilized in vitro while undergoing monitoring of calcium oscillatory patterns. Following parthenogenetic activation, superovulated eggs had a slightly delayed onset and longer duration of the first calcium transient, but no differences in oscillation persistence, frequency, or total calcium signal. However, in vitro fertilized superovulated eggs had no differences in any of these measures of calcium oscillatory behavior relative to spontaneously ovulated eggs. These findings indicate that although subtle differences in calcium signaling can be detected following parthenogenetic activation, superovulation does not disrupt physiological calcium signaling at fertilization, supporting the use of this method for both clinical and experimental purposes.Virginia SavyPaula SteinMin ShiCarmen J. WilliamsFrontiers Media S.A.articlesuperovulationoocytemousecalcium oscillationsegg activationBiology (General)QH301-705.5ENFrontiers in Cell and Developmental Biology, Vol 9 (2021)
institution DOAJ
collection DOAJ
language EN
topic superovulation
oocyte
mouse
calcium oscillations
egg activation
Biology (General)
QH301-705.5
spellingShingle superovulation
oocyte
mouse
calcium oscillations
egg activation
Biology (General)
QH301-705.5
Virginia Savy
Paula Stein
Min Shi
Carmen J. Williams
Superovulation Does Not Alter Calcium Oscillations Following Fertilization
description Superovulation is a common approach to maximize the number of eggs available for either clinical assisted reproductive technologies or experimental animal studies. This procedure provides supraphysiological amounts of gonadotropins to promote continued growth and maturation of ovarian follicles that otherwise would undergo atresia. There is evidence in mice, cows, sheep, and humans that superovulation has a detrimental impact on the quality of the resulting ovulated eggs or embryos. Here we tested the hypothesis that eggs derived from superovulation have a reduced capacity to support calcium oscillations, which are a critical factor in the success of embryo development. Eggs were obtained from mice that were either naturally cycling or underwent a standard superovulation protocol. The eggs were either parthenogenetically activated using strontium or fertilized in vitro while undergoing monitoring of calcium oscillatory patterns. Following parthenogenetic activation, superovulated eggs had a slightly delayed onset and longer duration of the first calcium transient, but no differences in oscillation persistence, frequency, or total calcium signal. However, in vitro fertilized superovulated eggs had no differences in any of these measures of calcium oscillatory behavior relative to spontaneously ovulated eggs. These findings indicate that although subtle differences in calcium signaling can be detected following parthenogenetic activation, superovulation does not disrupt physiological calcium signaling at fertilization, supporting the use of this method for both clinical and experimental purposes.
format article
author Virginia Savy
Paula Stein
Min Shi
Carmen J. Williams
author_facet Virginia Savy
Paula Stein
Min Shi
Carmen J. Williams
author_sort Virginia Savy
title Superovulation Does Not Alter Calcium Oscillations Following Fertilization
title_short Superovulation Does Not Alter Calcium Oscillations Following Fertilization
title_full Superovulation Does Not Alter Calcium Oscillations Following Fertilization
title_fullStr Superovulation Does Not Alter Calcium Oscillations Following Fertilization
title_full_unstemmed Superovulation Does Not Alter Calcium Oscillations Following Fertilization
title_sort superovulation does not alter calcium oscillations following fertilization
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/f48dc4fad44143398b076c1ae1356685
work_keys_str_mv AT virginiasavy superovulationdoesnotaltercalciumoscillationsfollowingfertilization
AT paulastein superovulationdoesnotaltercalciumoscillationsfollowingfertilization
AT minshi superovulationdoesnotaltercalciumoscillationsfollowingfertilization
AT carmenjwilliams superovulationdoesnotaltercalciumoscillationsfollowingfertilization
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