Related Experiment Videos
Bovine embryo culture in vitro: new developments and post-transfer consequences
1Reproductive Technologies Group, AgResearch Ruakura Research Centre, Hamilton, New Zealand. jeremy.thompson@adelaide.edu.au
Human Reproduction (Oxford, England)
|March 27, 2001
Summary
Sequential media improve cattle blastocyst production, but protein-free systems are metabolically compromising. Metabolic inhibitors and low oxygen enhance embryo development, yet fetal loss and oversize remain challenges.
Area of Science:
- Reproductive biology
- Developmental biology
- Animal science
Background:
- Cattle blastocyst production has shifted from co-culture to sequential media systems, improving performance.
- Wholly defined, protein-free systems compromise cattle blastocyst metabolic function.
- Metabolic inhibitors and low oxygen are novel strategies for in vitro embryo development.
Purpose of the Study:
- To evaluate the impact of metabolic inhibitors and low oxygen on cattle blastocyst development in vitro.
- To investigate the causes of post-implantation fetal loss and fetal oversize in cattle embryo culture.
- To identify potential mechanisms linking allantoic development failure to fetal oversize.
Main Methods:
- In vitro culture of cattle embryos using sequential media.
- Application of metabolic inhibitors (NaN3, 2,4-dinitrophenol) and low oxygen (2%) during the peri-compaction period.
- Analysis of blastocyst yield and quality.
- Examination of fetal development and conceptus viability up to day 110, focusing on allantoic development.
Main Results:
- Metabolic inhibitors and low oxygen significantly increased blastocyst yield (10-20%) and quality.
- Despite improvements, cattle embryo culture is associated with fetal oversize and significant post-day 35 fetal loss.
- Fetal loss is linked to impaired allantoic development, potentially due to poor nutrient supply and waste removal.
Conclusions:
- Sequential media and specific in vitro treatments can enhance cattle blastocyst production.
- Significant challenges remain, including metabolic compromise in protein-free systems and post-implantation fetal loss.
- Disrupted allantoic development is a key factor in fetal loss and may be related to fetal oversize syndrome.