Related Experiment Videos
Human chorionic gonadotrophin: embryonic secretion is a time-dependent phenomenon
B J Woodward1, E A Lenton, K Turner
1Sheffield Fertility Centre, UK.
Human Reproduction (Oxford, England)
|September 1, 1993
Summary
Human chorionic gonadotropin (HCG) secretion by human pre-embryos is time-dependent and not dependent on hatching. Intrazonal blastocysts can secrete sufficient HCG for early embryonic recognition.
Area of Science:
- Reproductive biology
- Embryology
- Biochemistry
Background:
- Human chorionic gonadotropin (HCG) is a key hormone in early pregnancy.
- Understanding HCG secretion dynamics in vitro is crucial for assessing pre-embryo viability.
Purpose of the Study:
- To investigate the timing and patterns of human chorionic gonadotropin (HCG) secretion by human pre-embryos in vitro.
- To determine the relationship between HCG secretion, blastocyst development, and hatching status.
- To compare HCG secretion rates in vitro with in vivo data.
Main Methods:
- Cultured 48 spare human pre-embryos to the expanded blastocyst stage.
- Measured human chorionic gonadotropin (HCG) levels in culture supernatant.
- Monitored blastocyst development, including zona pellucida status (intrazonal, partially hatched, fully hatched).
- Analyzed HCG secretion over time and calculated doubling times.
Main Results:
- 45.6% of expanded blastocysts secreted significant HCG (> 5 IU/l/day).
- HCG secretion was time-dependent, starting around 160 hours post-insemination and increasing exponentially.
- Hatching was not required for HCG secretion; intrazonal blastocysts produced similar amounts.
- Blastocysts from abnormally fertilized oocytes showed delayed and lower HCG secretion.
- In vitro HCG doubling times were rapid (< 10 hours for 86.4% of blastocysts).
Conclusions:
- Human pre-embryo HCG secretion is a viable marker of developmental potential.
- Intrazonal blastocysts can produce sufficient HCG for early embryonic recognition.
- The ability to escape the zona pellucida may be a critical factor for pre-embryo implantation potential.