Blastocyst development of 4-cell mouse embryos after laser destruction of one blastomere with or without its microsurgical removal

Aim: To study the rate of blastocyst formation in 4-cell mouse embryos after laser destruction of one blastomere, with or without microsurgical removal of the destroyed blastomere. Methods: Mouse embryos were randomly allocated to two control and two experimented groups. Control embryos were either...

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Main Authors: Teraporn Vutyavanich, Patcharada Amatyakul, Waraporn Piromlertamorn
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/61877
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spelling th-cmuir.6653943832-618772018-09-11T09:00:36Z Blastocyst development of 4-cell mouse embryos after laser destruction of one blastomere with or without its microsurgical removal Teraporn Vutyavanich Patcharada Amatyakul Waraporn Piromlertamorn Medicine Aim: To study the rate of blastocyst formation in 4-cell mouse embryos after laser destruction of one blastomere, with or without microsurgical removal of the destroyed blastomere. Methods: Mouse embryos were randomly allocated to two control and two experimented groups. Control embryos were either non-manipulated (117 embryos) or underwent laser ablation of zona only (114 embryos). Experimented embryos had laser destruction of zona and the adjacent blastomeres. Destroyed blastomeres were either left in situ (115 embryos) or were microsurgically removed (107 embryos). They were cultured in sequential media for 72 h and were assessed for cleavage/morula arrest and blastocyst formation rates. Results: Embryos arrested at cleavage/morula stages were higher when destroyed blastomeres remained in situ (30.4%) than when they were immediately removed (15.0%, P < 0.05). Blastocysts in the group with immediate removal of the destroyed blastomeres (85%) were significantly higher than when destroyed blastomeres were left in situ (69.6%, P < 0.05). Blastocyst formation in the repaired embryos was significantly lower than the non-manipulated (91.5%) and the manipulated controls (94.8%, P < 0.05). Hatching blastocysts were highest in control embryos with zonal ablation (72.8%). Proportions of hatching/hatched blastocysts in embryos, with or without removal of destroyed blastomeres, were not significantly different (39.3% and 33.9%, respectively). The percentage of embryonic loss during an attempt at microsurgical repair was 6.1%. Conclusion: Microsurgical removal of destroyed blastomere was effective in restoring blastocyst development. It could reduce the rate of cleavage/morula arrest. © 2006 Japan Society of Obstetrics and Gynecology. 2018-09-11T09:00:36Z 2018-09-11T09:00:36Z 2006-04-01 Journal 14470756 13418076 2-s2.0-33645091926 10.1111/j.1447-0756.2006.00371.x https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33645091926&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/61877
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Medicine
spellingShingle Medicine
Teraporn Vutyavanich
Patcharada Amatyakul
Waraporn Piromlertamorn
Blastocyst development of 4-cell mouse embryos after laser destruction of one blastomere with or without its microsurgical removal
description Aim: To study the rate of blastocyst formation in 4-cell mouse embryos after laser destruction of one blastomere, with or without microsurgical removal of the destroyed blastomere. Methods: Mouse embryos were randomly allocated to two control and two experimented groups. Control embryos were either non-manipulated (117 embryos) or underwent laser ablation of zona only (114 embryos). Experimented embryos had laser destruction of zona and the adjacent blastomeres. Destroyed blastomeres were either left in situ (115 embryos) or were microsurgically removed (107 embryos). They were cultured in sequential media for 72 h and were assessed for cleavage/morula arrest and blastocyst formation rates. Results: Embryos arrested at cleavage/morula stages were higher when destroyed blastomeres remained in situ (30.4%) than when they were immediately removed (15.0%, P < 0.05). Blastocysts in the group with immediate removal of the destroyed blastomeres (85%) were significantly higher than when destroyed blastomeres were left in situ (69.6%, P < 0.05). Blastocyst formation in the repaired embryos was significantly lower than the non-manipulated (91.5%) and the manipulated controls (94.8%, P < 0.05). Hatching blastocysts were highest in control embryos with zonal ablation (72.8%). Proportions of hatching/hatched blastocysts in embryos, with or without removal of destroyed blastomeres, were not significantly different (39.3% and 33.9%, respectively). The percentage of embryonic loss during an attempt at microsurgical repair was 6.1%. Conclusion: Microsurgical removal of destroyed blastomere was effective in restoring blastocyst development. It could reduce the rate of cleavage/morula arrest. © 2006 Japan Society of Obstetrics and Gynecology.
format Journal
author Teraporn Vutyavanich
Patcharada Amatyakul
Waraporn Piromlertamorn
author_facet Teraporn Vutyavanich
Patcharada Amatyakul
Waraporn Piromlertamorn
author_sort Teraporn Vutyavanich
title Blastocyst development of 4-cell mouse embryos after laser destruction of one blastomere with or without its microsurgical removal
title_short Blastocyst development of 4-cell mouse embryos after laser destruction of one blastomere with or without its microsurgical removal
title_full Blastocyst development of 4-cell mouse embryos after laser destruction of one blastomere with or without its microsurgical removal
title_fullStr Blastocyst development of 4-cell mouse embryos after laser destruction of one blastomere with or without its microsurgical removal
title_full_unstemmed Blastocyst development of 4-cell mouse embryos after laser destruction of one blastomere with or without its microsurgical removal
title_sort blastocyst development of 4-cell mouse embryos after laser destruction of one blastomere with or without its microsurgical removal
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33645091926&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/61877
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