Comparison of different cryopreservation methods for horse and donkey embryos

被引:13
作者
Perez-Marin, C. C. [1 ]
Vizuete, G. [1 ]
Vazquez-Martinez, R. [2 ]
Galisteo, J. J. [3 ]
机构
[1] Univ Cordoba, Dept Anim Med & Surg, Fac Vet Med, Cordoba, Spain
[2] Univ Cordoba, Dept Cellular Biol Physiol & Immunol, Cordoba, Spain
[3] Cria Caballar Ias FAS, Ctr Mil Cria Caballar Ecija, Seville, Spain
关键词
horse; vitrification; slow freezing; preservation; blastocyst; morula; jenny; mare; VITRIFIED EQUINE EMBRYOS; OPEN PULLED STRAW; IN-VITRO; ETHYLENE-GLYCOL; PREGNANCY RATES; VITRIFICATION; BLASTOCYSTS; APOPTOSIS; CAPSULE; MARES;
D O I
10.1111/evj.12777
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
BackgroundFew studies have been published about cryopreservation and embryo assessment in horses and donkeys. ObjectivesTo evaluate the viability of embryos collected from mares and jennies that were cryopreserved by slow freezing or by vitrification. Study designRandomised controlled experiment. MethodsHorse (n=19) and donkey (n=16) embryos (300 m) were recovered on days 6.5-7.5 post-ovulation and assigned to control or cryopreservation protocols of slow freezing or vitrification. For slow freezing, 1.5 mol/L ethylene glycol (EG) was used. For vitrification, horse embryos were exposed to 1.4 mol/L glycerol, 1.4 mol/L glycerol + 3.6 mol/L EG and 3.4 mol/L glycerol + 4.6 mol/L EG, using Fibreplug or a 0.25 mL straw; donkey embryos were vitrified using Fibreplug with similar EG-glycerol solutions to above or 7.0 mol/L EG. Dead cells, apoptotic and fragmented nuclei, and cytoskeleton quality were assessed on thawed/warmed embryos. ResultsA significant decrease in embryo quality was observed after cryopreservation (P<0.05). Although the percentage of dead cells was lower (P<0.05) in control than in cryopreserved embryos, no differences were observed between freezing protocols used for horse or donkey embryos. While no differences were detected in the number of apoptotic cells in warmed horse embryos, in donkey embryos a higher incidence of apoptosis was measured after vitrification with EG-glycerol in Fibreplug (P<0.05). Vitrified horse embryos had a significantly (P<0.05) higher percentage of nonviable cells than donkey embryo. Actin cytoskeleton quality did not differ between treatments. Main limitationsDifficulties in obtaining a large number of embryos meant that the number of embryos per group was low. ConclusionsVitrified horse and donkey embryos did not show higher susceptibility to cell damage than those preserved by slow freezing, whether using straws or Fibreplug. However, Fibreplug with EG 7 mol/L resulted in fewer nonviable and apoptotic cells in donkey embryos. Donkey embryos showed lower susceptibility to vitrification than horse embryos. The Summary is available in Spanish - See Supporting Information
引用
收藏
页码:398 / 404
页数:7
相关论文
共 30 条
[1]   Effect of dehydration prior to cryopreservation of large equine embryos [J].
Barfield, J. P. ;
McCue, P. M. ;
Squires, E. L. ;
Seidel, G. E., Jr. .
CRYOBIOLOGY, 2009, 59 (01) :36-41
[2]  
Bruyas J F, 2000, J Reprod Fertil Suppl, P549
[3]   Successful cryopreservation of expanded equine blastocysts [J].
Choi, Y. H. ;
Velez, I. C. ;
Riera, F. L. ;
Roldan, J. E. ;
Hartman, D. L. ;
Bliss, S. B. ;
Blanchard, T. L. ;
Hayden, S. S. ;
Hinrichs, K. .
THERIOGENOLOGY, 2011, 76 (01) :143-152
[4]   Vitrification of in vitro-produced and in vivo-recovered equine blastocysts in a clinical program [J].
Choi, Young-Ho ;
Hinrichs, Katrin .
THERIOGENOLOGY, 2017, 87 :48-54
[5]   Cryopreservation of Day 8 equine embryos after blastocyst micromanipulation and vitrification [J].
Diaz, Fabian ;
Bondiolli, Kenneth ;
Paccamonti, Dale ;
Gentry, Glen T. .
THERIOGENOLOGY, 2016, 85 (05) :894-903
[6]   Establishment of pregnancies after serial dilution or direct transfer by vitrified equine embryos [J].
Eldridge-Panuska, WD ;
di Brienza, VC ;
Seidel, GE ;
Squires, EL ;
Carnevale, EM .
THERIOGENOLOGY, 2005, 63 (05) :1308-1319
[7]  
Hardy K, 1999, REV REPROD, V4, P125
[8]   Cellular damage suffered by equine embryos after exposure to cryoprotectants or cryopreservation by slow-freezing or vitrification [J].
Hendriks, W. K. ;
Roelen, B. A. J. ;
Colenbrander, B. ;
Stout, T. A. E. .
EQUINE VETERINARY JOURNAL, 2015, 47 (06) :701-707
[9]  
HENDRIKS WK, 2010, Animal Reproduction Science, V121, P279
[10]   Direct transfer of equine blastocysts frozen-thawed in the presence of ethylene glycol and sucrose [J].
Hochi, S ;
Maruyama, K ;
Oguri, N .
THERIOGENOLOGY, 1996, 46 (07) :1217-1224