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http://dx.doi.org/10.5713/ajas.2003.23

Survival and In Vitro Development of Immature Bovine Oocytes Cryopreserved by Vitrification  

Yang, Byoung-Chul (National Livestock Research Institute, RDA)
Im, Gi-Sun (National Livestock Research Institute, RDA)
Chang, Won-Kyong (National Livestock Research Institute, RDA)
Lee, Yun-Keun (National Livestock Research Institute, RDA)
Oh, Sung-Jong (National Livestock Research Institute, RDA)
Jin, Dong-Il (Department of Applied Biological Science, College of Natural Science, Sun Moon University)
Im, Kyong-Sun (School of Agricultural Biotechnology, Seoul National University)
Lee, Chang-Kyu (School of Agricultural Biotechnology, Seoul National University)
Publication Information
Asian-Australasian Journal of Animal Sciences / v.16, no.1, 2003 , pp. 23-28 More about this Journal
Abstract
The present study was undertaken to investigate the effects of PVP concentration and exposure temperature to vitrification solution on the post-thaw survival, in vitro maturation and development of immature bovine oocytes (germinal vesicle stage). The vitrification solution (VS) consisted of 40% ethylene glycol (EG)+0.5 M sucrose (S)+10% FBS. PVP was added to VS: 0%, 5% or 10%. The cumulus-oocyte complexes (COCs) were diluted in VS as one step, after 2 min the COCs were loaded in straw and vitrified by direct immersion into liquid nitrogen. For thawing, the straws were plunged into $30^{\circ}C$ water bath for 10s. After thawing, the oocytes were diluted in 0.5 M (in DPBS with 10% FBS) sucrose solution for 5 min. The survival rate (FDA-test and trypan blue) of immature bovine oocytes was measured. The survival rate was higher in 5% PVP (91.5%) than in 0% (64.2%) or in 10% PVP (79.7%). The proportion of metaphase II formation was 69.35% in control (no vitrified COCs), 9.3% in 40% EG+0.5 M S+0% PVP and 21.05% in 40% EG+0.5 M S+5% PVP (p<0.05). The effect of room temperature ($25^{\circ}C$ for 10 min) and cold temperature ($4^{\circ}C$ for 10 min) on COCs were determined in this study. After IVF, the cleavage and blastocysts rate of oocytes exposed to room temperature and cold temperature in VS+5% PVP was significantly different (2 cell: 63.20% vs 37.97%, blastocysts: 18.40% vs 2.53%). The cleavage rates of frozen-thawed oocytes were 20.53% with PVP and 22.13% without PVP (p>0.05). Two out of 151 oocytes (1.32%) developed to blastocyst stage after frozen-thawed with 5% PVP (p>0.05). Development of oocytes after frozen-thawing to the 2 cell were not significantly affected with or without PVP following IVF. However, the vitrification of immature bovine oocytes with PVP maintained the ability to develop to the blastocyst stage after IVM-IVF and IVC, while no blastocysts were obtained from oocytes vitrified without PVP. These results suggested that PVP has a protective role for vitrification of immature bovine oocytes as far as survival is concerned, however, the protection was not sufficient enough to support blastocyst formation.
Keywords
Bovine Immature Oocytes; Polyvinylpyrrolidone (PVP); Vitrification; Blastocyst;
Citations & Related Records

Times Cited By Web Of Science : 4  (Related Records In Web of Science)
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1 Ali, J. and J. N. Shelton. 1993b. Design of vitrification solutions for the cryopreservation of embryos. J. Reprod. Fertil. 99:471-477.   DOI
2 Arav, A., Y. Rubinsky, S. B. Leslie, E. Bechboodi, G. B. Anderson and J. H. Crowe. 1996. Phase transition temperature and chilling sensitivity of bovine oocytes. Cryobiology. 33:589-599.   DOI   ScienceOn
3 Fahy, G. M., D. R. MacFarlane, C. A. Angel and H. T. Meryman. 1994. Vitrification as an approach to cryopreservation. Cryobiology. 21:407-426.   DOI   ScienceOn
4 Herrler, A., D. Rath and H. Niemann. 1991. Effects of cryoprotectants on fertilization and cleavage of bovine oocytes in vitro. Theriogenology. 35:212(Abstr.).   DOI
5 Otoi, T., K. Yamamoto, N. Koyama, S. Tachikawa and T. Suzuki. 1998. Cryopreservation of mature bovine oocytes by vitrification in straws. Cryobiology. 37:77-85.   DOI   ScienceOn
6 Pellicer, A., A. Lightman, T. G. Parmer, H. R. Behrman and A. H. De Cherney. 1988. Morphologic and functional studies of immature rat oocyte-cumulus complexes after cryopreservation. Fertil. Steril. 50:805-810.   DOI
7 Poolard, J. W. and S. P. Leibo. 1994. Chilling sensitivity of mammalian embryos. Theriogenelogy. 4:101-106.
8 Rall, W. F. 1987. Factors affecting the survival of mouse embryos cryopreserved by vitrification. Cryobiology. 24:387-402.   DOI   PUBMED   ScienceOn
9 Suzuki, T. and Y. Nishikata. 1992. Fertilization and cleavage of frozen thawed bovine oocytes by one step dilution method in vitro. Theriogenology. 37:306(Abstr.).   DOI
10 Vajta, G., P. Holm, M. Kuwayama, P. J. Booth, H. Jacobsen, T. Greve and H. Callesen. 1998. Open pulled straw (OPS) vitrification: A new way to reduce cryoinjuries of bovine ova and embryos. Mol. Reprod. Dev. 51:53-58.   DOI   ScienceOn
11 Suzuki, T., A. Boediono, M. Takagi, S. Saha and C. Sumantri. 1996. Fertilization and development of frozen-thawed germinal vesicle bovine oocytes by an one-step dilution methods in vitro. Cryobiology. 33:515-524.   DOI   ScienceOn
12 Szell, A., J. Shelton and K. Szell. 1989. Osomotic characteristics of sheep and cattle embryos. Cryobiology. 26:297-302.   DOI   ScienceOn
13 Dhali, A., R. S. Manik, S. K. Das, S. K. Singla and P. Palta. 2000. Vitrification of buffalo (Bubalus bubalis) oocytes. Theriogenelogy. 53:1295-1303.   DOI   ScienceOn
14 Brackett, B. G. and G. Oliphant. 1975. Capacitation of rabbit spermatozoa in vitro. Biol. Reprod. 12:260-274.   DOI   ScienceOn
15 Linda, R. M. and A. O. Trounson. 1980. The use of fluorescein diacetate to assess embryo viability in the mouse. J. Reprod. Fertil. 58:189-196.   DOI
16 Szell, A. and J. N. Shelton. 1987. Osomotic and cryoprotective effect of glycerol sucrose solution on day-3 mouse embryos. J. Reprod. Fertil. 80:309 -316.   DOI
17 Fuku, E., L. Xia and B. R. Downey. 1995. Ultrastructural changes in bovine oocytes cryopreserved by vitrification. Cryobiology. 32:139-156.   DOI   ScienceOn
18 Martiano, A., W. P. John and S. P. Leibo. 1996. Effect of chilling bovine oocytes on their developmental competence. Mol. Reprod. Develop. 45:503-512.   DOI   ScienceOn
19 Ali, J. and J. N. Shelton. 1993a. Vitrification of preimplantation stages of mouse embryos. J. Reprod. Fertil. 98:459-465.   DOI
20 Rall, W. F. and G. M. Fahy. 1985. Ice-free cryopreservation of mouse embryos at $-196^{\circ}C$ by vitrification. Nature. 313:573-575.   DOI   ScienceOn
21 Takagi, M., A. Boediono, S. Saha and T. Suzuki. 1993. Survival rate of frozen-thawed bovine IVF embryos in relation to exposure time using various cryoprotectants. Cryobiology 30:306-312.   DOI   ScienceOn
22 Le Gal, F. and A. Massip. 1999. Cryopreservation of cattle oocytes: Effects of meiotic stage, cycloheximide treatment, and vitrification procedure. Cryopreservation. 38:290-300.
23 Didion, B. A., D. Pomp, M. J. Martin, G. E. Homanics and C. L. Markert. 1990. Observations on the cooling and cryopreservation of pig oocytes at the germinal vesicle stage. J. Anim. Sci. 68:2803-2810.
24 Lim, J. M., Y. Fukui and H. Ono. 1992. Developmental competence of bovine oocytes frozen at various maturation stages followed by in vitro maturation and fertilization. Theriogenology. 37:351-361.   DOI   ScienceOn
25 Kuleshova, L. L., D. R. MacFarlane, A. O. Trounson and J. M. Shaw. 1999. Sugars extract a major influence on the vitrification properties of ethylene glycol-based solutions and have low toxicity to embryos and oocytes. Cryobiology. 38:119-130.   DOI   ScienceOn
26 Voelkel, S. A. and Y. X. Hu. 1992. Direct transfer of frozenthawed bovine embryos. Theriogenology 37:23-37.   DOI   ScienceOn
27 Xu, K. O. and K. J. Betteridge. 1992. Cryopreservation of bovine oocytes using propylene glycol : Preliminary results. Theriogenology 37:324(Abstr.).   DOI