Related Experiment Video
Updated: Sep 20, 2026

Long-term Behavioral and Reproductive Consequences of Embryonic Exposure to Low-dose Toxicants
Published on: March 6, 2018
Developmental alterations in murine embryos exposed in vitro to an estrogenic pesticide, o,p'-DDT
A R Greenlee1, C A Quail, R L Berg
1National Farm Medicine Center, Marshfield Medical Research Foundation, Wisconsin 5449, USA. greenlea@mfldclin.edu
Abstract:
Culturing pronuclear embryos from CD-1 mice with o,p'-DDT and p,p'-DDT was examined as a means for directly evaluating toxicant risk and for increasing the speed of screening developmental toxicants. Pronuclear (2PN) embryos from CD-1 mice were cultured 96 h in modified Earle's balanced salt solution containing 0.1% (v/v) ethanol (control) or 10-fold dilutions of 17/beta-estradiol, o,p'-DDT, or p,p'-DDT. Compared to control treatment, 96 h incubation of 2PN embryos with 0.1 gg/mL o,p'-DDT significantly reduced embryo development to blastocyst and mean cell number, and increased the percentage of cells undergoing apoptosis. The effects of o,p'-DDT on developmental parameters were dose-responsive. Embryo sexing by multiplex polymerase chain reaction indicated that both sexes were susceptible to toxicant injury with comparable reduction in development to blastocyst (27% and 24%, respectively) in the presence of o,p'-DDT. Results of this study suggest that in vitro exposure of preimplantation embryos to xenobiotics may provide a useful tool for rapidly screening developmental toxicants.
Insights
Exposure to o,p'-DDT significantly harmed mouse embryo development, impacting blastocyst formation and cell count. This study suggests in vitro embryo culture is a fast method for screening developmental toxicants.
Area of Science:
- Developmental toxicology
- Reproductive toxicology
- In vitro toxicology
Background:
- Evaluating developmental toxicants is crucial for risk assessment.
- Rapid screening methods for developmental toxicants are needed.
- In vitro models offer potential for efficient toxicological evaluation.
Purpose of the Study:
- To assess the developmental toxicity of o,p '-DDT and p,p '-DDT using cultured mouse pronuclear embryos.
- To evaluate the utility of in vitro preimplantation embryo culture for rapid toxicant screening.
Main Methods:
- Pronuclear (2PN) mouse embryos were cultured for 96 hours.
- Embryos were exposed to ethanol (control), 17/beta-estradiol, o,p '-DDT, or p,p '-DDT.
- Developmental parameters (blastocyst formation, cell number, apoptosis) were assessed.
- Embryo sex was determined using multiplex polymerase chain reaction.
Main Results:
- o,p '-DDT exposure significantly reduced embryo development to blastocyst and mean cell number.
- Apoptosis increased in embryos exposed to o,p '-DDT in a dose-responsive manner.
- Both male and female embryos showed comparable susceptibility to o,p '-DDT toxicity.
Conclusions:
- In vitro culture of preimplantation embryos is a viable method for assessing developmental toxicant effects.
- This in vitro approach can accelerate the screening process for developmental toxicants.
- o,p '-DDT exhibits significant developmental toxicity in early mouse embryos.
Related Concept Videos
Oogenesis
Teratogenicity

