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Natural honey acts as a nonpermeating cryoprotectant for promoting bovine oocyte vitrification
Sugars are commonly supplemented into vitrification solution to dehydrate cells in order to reduce the formation of fatal intracellular ice crystals. Natural honey is a mixture of 25 sugars (mainly fructose and glucose) that have different biological and pharmacological benefits. The present study w...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467261/ https://www.ncbi.nlm.nih.gov/pubmed/32877463 http://dx.doi.org/10.1371/journal.pone.0238573 |
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author | Alfoteisy, Bilal Singh, Jaswant Anzar, Muhammad |
author_facet | Alfoteisy, Bilal Singh, Jaswant Anzar, Muhammad |
author_sort | Alfoteisy, Bilal |
collection | PubMed |
description | Sugars are commonly supplemented into vitrification solution to dehydrate cells in order to reduce the formation of fatal intracellular ice crystals. Natural honey is a mixture of 25 sugars (mainly fructose and glucose) that have different biological and pharmacological benefits. The present study was designed to determine if honey can be used as a nonpermeating cryoprotectant in vitrification of bovine oocytes. In the first experiment, denuded-MII oocytes were exposed to 0.25, 0.5, 1.0, 1.5 or 2.0 M of honey or sucrose. Natural honey and sucrose caused similar ooplasm dehydration. A significant relationship existed between time and ooplasm volume change (P < 0.05), during dehydration and rehydration phases, in both honey and sucrose solutions. In the second experiment, the immature cumulus-oocyte complexes (COCs) were vitrified in an EG/DMSO-based vitrification solution containing honey (0.5, 1 or 1.5 M) or sucrose (0.5 M) as a gold standard. The vitrified-warmed COCs were matured in vitro and evaluated for nuclear maturation. The maturation (MII) rate was greater in nonvitrified control (81%) than vitrified groups (54%, P < 0.05). In the third experiment, COCs were either remained nonvitrified (control) or vitrified in 1.0 M honey or 0.5 M sucrose, followed by IVM, IVF and IVC (for 9 days). Cleavage rate was greater in control (74%) than in vitrified groups (47%, P < 0.05), without significant difference between sugars. Blastocyst rate was 34, 13 and 3% in control, honey and sucrose groups respectively (P < 0.05). In conclusion, natural honey acted as a nonpermeating cryoprotectant in vitrification solution and improved the embryonic development in vitrified bovine COCs. |
format | Online Article Text |
id | pubmed-7467261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74672612020-09-11 Natural honey acts as a nonpermeating cryoprotectant for promoting bovine oocyte vitrification Alfoteisy, Bilal Singh, Jaswant Anzar, Muhammad PLoS One Research Article Sugars are commonly supplemented into vitrification solution to dehydrate cells in order to reduce the formation of fatal intracellular ice crystals. Natural honey is a mixture of 25 sugars (mainly fructose and glucose) that have different biological and pharmacological benefits. The present study was designed to determine if honey can be used as a nonpermeating cryoprotectant in vitrification of bovine oocytes. In the first experiment, denuded-MII oocytes were exposed to 0.25, 0.5, 1.0, 1.5 or 2.0 M of honey or sucrose. Natural honey and sucrose caused similar ooplasm dehydration. A significant relationship existed between time and ooplasm volume change (P < 0.05), during dehydration and rehydration phases, in both honey and sucrose solutions. In the second experiment, the immature cumulus-oocyte complexes (COCs) were vitrified in an EG/DMSO-based vitrification solution containing honey (0.5, 1 or 1.5 M) or sucrose (0.5 M) as a gold standard. The vitrified-warmed COCs were matured in vitro and evaluated for nuclear maturation. The maturation (MII) rate was greater in nonvitrified control (81%) than vitrified groups (54%, P < 0.05). In the third experiment, COCs were either remained nonvitrified (control) or vitrified in 1.0 M honey or 0.5 M sucrose, followed by IVM, IVF and IVC (for 9 days). Cleavage rate was greater in control (74%) than in vitrified groups (47%, P < 0.05), without significant difference between sugars. Blastocyst rate was 34, 13 and 3% in control, honey and sucrose groups respectively (P < 0.05). In conclusion, natural honey acted as a nonpermeating cryoprotectant in vitrification solution and improved the embryonic development in vitrified bovine COCs. Public Library of Science 2020-09-02 /pmc/articles/PMC7467261/ /pubmed/32877463 http://dx.doi.org/10.1371/journal.pone.0238573 Text en © 2020 Alfoteisy et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Alfoteisy, Bilal Singh, Jaswant Anzar, Muhammad Natural honey acts as a nonpermeating cryoprotectant for promoting bovine oocyte vitrification |
title | Natural honey acts as a nonpermeating cryoprotectant for promoting bovine oocyte vitrification |
title_full | Natural honey acts as a nonpermeating cryoprotectant for promoting bovine oocyte vitrification |
title_fullStr | Natural honey acts as a nonpermeating cryoprotectant for promoting bovine oocyte vitrification |
title_full_unstemmed | Natural honey acts as a nonpermeating cryoprotectant for promoting bovine oocyte vitrification |
title_short | Natural honey acts as a nonpermeating cryoprotectant for promoting bovine oocyte vitrification |
title_sort | natural honey acts as a nonpermeating cryoprotectant for promoting bovine oocyte vitrification |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467261/ https://www.ncbi.nlm.nih.gov/pubmed/32877463 http://dx.doi.org/10.1371/journal.pone.0238573 |
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