Comparison of Ham’s F10 with CO2 or Hepes buffer for storage of equine embryos at 5 C for 24 H.
Abstract: Forty equine embryos collected 7 d post-ovulation were stored at 5 C for 24 h in one of two culture media (n = 20/group): 1) Ham's F10 + 10% heat-treated fetal calf serum (FCS) buffered by gassing with 5% CO2, 5% O2 and 90% N2 and 2) Ham's F10 + 10% FCS with Hepes buffer (25 mM). Embryos cultured in Ham's F10 + CO2 maintained a better quality score and had a larger average increase in diameter (+34.8 micron) than embryos stored in Hepes buffered Ham's F10 (-10.2 micron). Embryos were transferred surgically into recipient mares that ovulated -3 to +1 d in relation to the donor mare. Twenty embryos cultured in Dulbecco's phosphate buffered saline + 10% FCS and transferred less than 1 h after collection were used as controls. Pregnancy rates were higher (P less than .05) for embryos stored in Ham's F10 + CO2 (70%, 55%) than for embryos stored in Ham's F10 + Hepes (20%, 15%) at 14 and 35 d, respectively. At 14 d, pregnancy rates for control embryos (90%) were similar (P greater than .05) to pregnancy rates for embryos cultured in Ham's F10 + CO2 (70%); however, by 35 d, pregnancy rates were higher (P less than .05) for controls (80%) than for embryos stored in Ham's F10 + CO2 (55%). It was concluded that Ham's F10 + CO2 was superior to Ham's F10 + Hepes for short-term storage of equine embryos at 5 C, and that satisfactory pregnancy rates could be obtained from transfer of embryos stored in Ham's F10 + CO2 at 5 C for 24 h.
Publication Date: 1987-12-01 PubMed ID: 3443591DOI: 10.2527/jas1987.6561775xGoogle Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.
This research compared two different storage methods for horse embryos, finding that the use of Ham’s F10 medium in combination with CO2 proves more effective than Hepes buffer for storing these embryos at a cooled temperature for 24 hours.
Study Design and Materials
- The study used 40 horse embryos, which were collected seven days post-ovulation.
- The embryos were divided into two groups and stored at 5 degrees Celsius for 24 hours.
- Two different storage mediums were used: 1) Ham’s F10 + 10% heat-treated fetal calf serum buffered by CO2, O2, and N2 and 2) Ham’s F10 + 10% fetal calf serum with Hepes buffer.
Criteria of Evaluation and Metrics
- The quality of the embryos and change in their diameter were tracked as indicators of the success of the storage method.
- Embryos stored in the CO2 medium had a higher quality score and a larger average increase in diameter compared with those stored in Hepes buffered medium.
- Post-storage, the embryos were surgically transferred into recipient mares, who had ovulated within a three-day window of the original donor mare.
- Success of the storage mediums was then determined by measuring pregnancy rates in the recipient mares at 14 and 35 days post-transfer.
Findings and Conclusion
- Embyos stored in the Ham’s F10 + CO2 medium had a significantly higher pregnancy success rate (70% and 55% at 14 and 35 days, respectively) compared with the embryos stored in the Ham’s F10 + Hepes medium (20% and 15% at 14 and 35 days, respectively).
- As a control, 20 embryos were kept in Dulbecco’s phosphate buffered saline + 10% FCS and transferred under an hour after collection. The success rate of these control embryos was not significantly different from those stored in the CO2 medium at 14 days, but was higher at 35 days.
- The study concluded that using the Ham’s F10 in combination with CO2 as a storage medium was superior to using Hepes buffer for short-term storage of horse embryos. Furthermore, this method produced satisfactory pregnancy rates when the embryos were stored at 5 degrees Celsius for 24 hours.
Cite This Article
APA
Carnevale EM, Squires EL, McKinnon AO.
(1987).
Comparison of Ham’s F10 with CO2 or Hepes buffer for storage of equine embryos at 5 C for 24 H.
J Anim Sci, 65(6), 1775-1781.
https://doi.org/10.2527/jas1987.6561775x Publication
Researcher Affiliations
- Anim. Reprod. Lab., Colorado State University, Fort Collins 80523.
MeSH Terms
- Animals
- Buffers
- Culture Media
- Embryo Transfer / veterinary
- Female
- HEPES
- Horses / embryology
- Tissue Preservation / veterinary
Citations
This article has been cited 3 times.- Benammar A, Derisoud E, Vialard F, Palmer E, Ayoubi JM, Poulain M, Chavatte-Palmer P. The Mare: A Pertinent Model for Human Assisted Reproductive Technologies?. Animals (Basel) 2021 Aug 4;11(8).
- de Dios Hourcade J, Pérez-Crespo M, Serrano A, Gutiérrez-Adán A, Pintado B. In vitro and in vivo development of mice morulae after storage in non-frozen conditions. Reprod Biol Endocrinol 2012 Aug 22;10:62.
- Poitras P, Guay P, Vaillancourt D, Zidane N, Bigras-Poulin M. In vitro viability of cryopreserved equine embryos following different freezing protocols. Can J Vet Res 1994 Oct;58(4):235-41.
Use Nutrition Calculator
Check if your horse's diet meets their nutrition requirements with our easy-to-use tool Check your horse's diet with our easy-to-use tool
Talk to a Nutritionist
Discuss your horse's feeding plan with our experts over a free phone consultation Discuss your horse's diet over a phone consultation
Submit Diet Evaluation
Get a customized feeding plan for your horse formulated by our equine nutritionists Get a custom feeding plan formulated by our nutritionists