Piglets born after vitrification of embryos using the open pulled straw method

Citation
F. Berthelot et al., Piglets born after vitrification of embryos using the open pulled straw method, CRYOBIOLOGY, 41(2), 2000, pp. 116-124
Citations number
35
Categorie Soggetti
Experimental Biology
Journal title
CRYOBIOLOGY
ISSN journal
00112240 → ACNP
Volume
41
Issue
2
Year of publication
2000
Pages
116 - 124
Database
ISI
SICI code
0011-2240(200009)41:2<116:PBAVOE>2.0.ZU;2-J
Abstract
Morulae and unhatched blastocysts from Large White hyperprolific (LWh) and Meishan (MS) gifts were selected to test an ultrarapid open pulled straw (O PS) vitrification method with two media, The viability of vitrified/warmed embryos was estimated by the percentage of embryos that developed to the ha tched blastocyst stage in vitro or by birth after transfer. In Experiment 1 , two cryoprotectant dilution media were compared for cryopreservation of M S and LWh blastocysts: TCM was a standard Hepes-buffered TCM199 + 20% NBCS medium and PBS was a PBS + 20% NBCS medium. After a two-step equilibration in ethylene glycol, dimethyl sulfoxide, and sucrose, 2-5 blastocysts were l oaded into OPS and plunged into liquid nitrogen. Embryos were warmed: a fou r-step dilution with decreasing concentrations of sucrose was applied. In P BS, LWh blastocysts (27%) had a lower viability in vitro than MS blastocyst s (67%; P = 0.001). In TCM, no significant difference was observed between genotypes (41% for LWh and 43% for MS blastocysts) and both viability rates were lower than that of the control groups. In Experiment 2, morula-stage LWh and MS embryos were vitrified and warmed using PBS. The viability rate was low and did not differ between LWh (11%) and MS (14%). In Experiment 3, 200 MS and 200 LWh blastocysts were vitrified/warmed as described in Exper iment 1 (PBS). In each of 20 MS recipients, 20 embryos were transferred. Th e farrowing rate was 55% and recipients farrowed four and five piglets (med ian) for MS and LWh blastocysts, respectively. The OPS method is therefore appropriate for cryopreservation of unhatched porcine blastocysts. (C) 2000 Academic Press.