Ontology highlight
ABSTRACT: Background
Many pesticides can antagonize the androgen receptor (AR) or inhibit androgen synthesis in vitro but their potential to cause reproductive toxicity related to disruption of androgen action during fetal life is difficult to predict. Currently no approaches for using in vitro data to anticipate such in vivo effects exist. Prioritization schemes that limit unnecessary in vivo testing are urgently needed.Objectives
The aim was to develop a quantitative in vitro to in vivo extrapolation (QIVIVE) approach for predicting in vivo anti-androgenicity arising from gestational exposures and manifesting as a shortened anogenital distance (AGD) in male rats.Methods
We built a physiologically based pharmacokinetic (PBK) m
SUBMITTER: Scholze M
PROVIDER: S-EPMC7687371 | biostudies-literature | 2020 Nov
REPOSITORIES: biostudies-literature