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. Author manuscript; available in PMC: 2019 Jun 1.
Published in final edited form as: Best Pract Res Clin Endocrinol Metab. 2018 Apr 6;32(3):283–297. doi: 10.1016/j.beem.2018.03.011

Table 2.

Considerations in Animal Model Selection and Use for EDC Research

  • Account for possible species differences in metabolism and generation of biologically active metabolites.

  • Select the most sensitive species possible.

  • Ensure the presence of a relevant target (a similar mechanism of action).

  • Ensure the outcome is relevant for human disease and not unique to that species (some types of cancers in rodents are not seen in humans).

  • Use both sexes – unless only one is relevant (prostate cancer).

  • Make sure dosing occurs over the appropriate critical period for that species.

  • Be aware that for EDCs latency between exposure and effect could be long and stretch into advanced adulthood.

  • Make sure enough individuals are used to have sufficient statistical power. For mammalian developmental toxicology studies the litter should be the statistical unit, not the individual pup.