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Assessment of Embryotoxicity Using Mouse Embryo Culture

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Part of the book series: Methods in Molecular Biology ((MIMB,volume 550))

Abstract

The mouse embryo culture technique is a valuable tool for assessing embryotoxicity of exogenous compounds as it excludes any confounding maternal and placental effects, allows for the selection of embryos that are at similar stages of development, and permits the control of exposure concentrations of exogenous agents and modifiers of interest. This chapter will use the anticonvulsant drug valproic acid as a model teratogen to describe the mouse embryo culture in detail. Briefly, mice are bred and the presence of a vaginal plug in a female mouse indicates gestational day (GD) 1. On GD 9 embryos are explanted from pregnant dams and embryos that are at similar stages of development (4–6 somite pairs) are cultured in CO2 saturated male rat serum for 24 h at 37°C. After 24 h embryonic morphological and developmental parameters, including anterior neuropore closure, are evaluated using a dissecting microscope. Additional biochemical analysis, including molecular approaches to assess embryonic signal transduction, as well as some limitations of the technique will also be discussed.

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© 2009 Humana Press, a part of Springer Science+Business Media, LLC

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Winn, L.M., Tung, E.W. (2009). Assessment of Embryotoxicity Using Mouse Embryo Culture. In: Vaillancourt, C., Lafond, J. (eds) Human Embryogenesis. Methods in Molecular Biology, vol 550. Humana Press. https://doi.org/10.1007/978-1-60327-009-0_15

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  • DOI: https://doi.org/10.1007/978-1-60327-009-0_15

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  • Publisher Name: Humana Press

  • Print ISBN: 978-1-60327-008-3

  • Online ISBN: 978-1-60327-009-0

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