Viability of bovine opu-derived oocytes to honeybee as cryoprotectant

This study designs to determine the effectiveness of Honeybee (HB) as cryoprotectants (CP) on viability vitrified-thawed bovine oocytes derived from OPU using Trehalose as control. Cattles were subjected to superstimulation protocol, per session conducted five days where three days both cattle were...

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Main Authors: Jie, T.C., Rahman, M.M., Pitchayapipatkul, J., Mashitah, S.M., Nor Azlina, A.A., Raja Ili Airina, R.K.
Format: Conference or Workshop Item
Published: 2021
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Online Access:http://eprints.um.edu.my/36026/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85107175775&doi=10.1088%2f1755-1315%2f756%2f1%2f012063&partnerID=40&md5=1b646c75f90cb3637bf56f2d35251d80
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spelling my.um.eprints.360262024-07-11T07:38:10Z http://eprints.um.edu.my/36026/ Viability of bovine opu-derived oocytes to honeybee as cryoprotectant Jie, T.C. Rahman, M.M. Pitchayapipatkul, J. Mashitah, S.M. Nor Azlina, A.A. Raja Ili Airina, R.K. Q Science (General) This study designs to determine the effectiveness of Honeybee (HB) as cryoprotectants (CP) on viability vitrified-thawed bovine oocytes derived from OPU using Trehalose as control. Cattles were subjected to superstimulation protocol, per session conducted five days where three days both cattle were administrated 100 mg follicle stimulation hormone (FSH) within 24 h once and two days of "resting period" totalling two sessions. The "coasting period" (FSH starvation) between sessions was four days (96 h). Oocytes collection via OPU were performed at fifth day (120 h). The ovarian growth was observed via ultrasonographic before OPU. Prior to vitrifying oocytes with treatment Trehalose (T1) and HB (T2) followed by warming protocol, oocytes subjected to in vitro maturation (IVM). Oocytes viability were evaluated by fluorescein diacetate staining. Results showed ovarian growth for first session was larger size follicles than the second session for both cattle. Total number of oocytes obtained were 60. Oocytes viability treatment T2 was significantly higher (90.9) than T1 (70.4). This study concludes that HB as CP in vitrification protocol was able to achieved high oocytes viability with oocytes derived via OPU suggesting Honeybee as an alternative CP for oocytes vitrification. © 2021 Institute of Physics Publishing. All rights reserved. 2021 Conference or Workshop Item PeerReviewed Jie, T.C. and Rahman, M.M. and Pitchayapipatkul, J. and Mashitah, S.M. and Nor Azlina, A.A. and Raja Ili Airina, R.K. (2021) Viability of bovine opu-derived oocytes to honeybee as cryoprotectant. In: 3rd Asia Pacific Regional Conference on Food Security, ARCoFS 2021, 9 March 2021, Kelantan, Virtual. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85107175775&doi=10.1088%2f1755-1315%2f756%2f1%2f012063&partnerID=40&md5=1b646c75f90cb3637bf56f2d35251d80
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic Q Science (General)
spellingShingle Q Science (General)
Jie, T.C.
Rahman, M.M.
Pitchayapipatkul, J.
Mashitah, S.M.
Nor Azlina, A.A.
Raja Ili Airina, R.K.
Viability of bovine opu-derived oocytes to honeybee as cryoprotectant
description This study designs to determine the effectiveness of Honeybee (HB) as cryoprotectants (CP) on viability vitrified-thawed bovine oocytes derived from OPU using Trehalose as control. Cattles were subjected to superstimulation protocol, per session conducted five days where three days both cattle were administrated 100 mg follicle stimulation hormone (FSH) within 24 h once and two days of "resting period" totalling two sessions. The "coasting period" (FSH starvation) between sessions was four days (96 h). Oocytes collection via OPU were performed at fifth day (120 h). The ovarian growth was observed via ultrasonographic before OPU. Prior to vitrifying oocytes with treatment Trehalose (T1) and HB (T2) followed by warming protocol, oocytes subjected to in vitro maturation (IVM). Oocytes viability were evaluated by fluorescein diacetate staining. Results showed ovarian growth for first session was larger size follicles than the second session for both cattle. Total number of oocytes obtained were 60. Oocytes viability treatment T2 was significantly higher (90.9) than T1 (70.4). This study concludes that HB as CP in vitrification protocol was able to achieved high oocytes viability with oocytes derived via OPU suggesting Honeybee as an alternative CP for oocytes vitrification. © 2021 Institute of Physics Publishing. All rights reserved.
format Conference or Workshop Item
author Jie, T.C.
Rahman, M.M.
Pitchayapipatkul, J.
Mashitah, S.M.
Nor Azlina, A.A.
Raja Ili Airina, R.K.
author_facet Jie, T.C.
Rahman, M.M.
Pitchayapipatkul, J.
Mashitah, S.M.
Nor Azlina, A.A.
Raja Ili Airina, R.K.
author_sort Jie, T.C.
title Viability of bovine opu-derived oocytes to honeybee as cryoprotectant
title_short Viability of bovine opu-derived oocytes to honeybee as cryoprotectant
title_full Viability of bovine opu-derived oocytes to honeybee as cryoprotectant
title_fullStr Viability of bovine opu-derived oocytes to honeybee as cryoprotectant
title_full_unstemmed Viability of bovine opu-derived oocytes to honeybee as cryoprotectant
title_sort viability of bovine opu-derived oocytes to honeybee as cryoprotectant
publishDate 2021
url http://eprints.um.edu.my/36026/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85107175775&doi=10.1088%2f1755-1315%2f756%2f1%2f012063&partnerID=40&md5=1b646c75f90cb3637bf56f2d35251d80
_version_ 1805881093574885376
score 13.189132