| Literature DB >> 29940329 |
Céline Pique1, Edward Marsden2, Paul Quesada2, Audrey Blondel2, Lars Friis Mikkelsen3.
Abstract
The minipig is accepted from scientific and regulatory perspectives for the safety evaluation of drug candidates on embryo-fetal development. The relative size and the duration of gestation (112-115 days) in the minipig is, however, considered a drawback compared with routine smaller species. We evaluated if study duration and cost could be optimized without impacting scientific validity by performing all terminal procedures around mid-gestation (60 days). At this stage, minipig fetal size is not too dissimilar to full term rabbit and therefore better suited to fetal processing/examination compared with at the end of gestation. Despite encountering higher than anticipated embryo-fetal death, morphological defects clearly associated with a known teratogen, pyrimethamine, were detected. Although the gonads are poorly differentiated macroscopically at mid-term, a histological examination confirmed that external sexing of the fetuses was accurate. Double staining of the bone and cartilage of the mid-term fetal skeleton allowed a more refined examination.Entities:
Keywords: Embryo-fetal development study; Mid-term fetal examinations; Minipig; Pyrimethamine; Skeleton double staining
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Year: 2018 PMID: 29940329 DOI: 10.1016/j.reprotox.2018.06.009
Source DB: PubMed Journal: Reprod Toxicol ISSN: 0890-6238 Impact factor: 3.143