| Literature DB >> 23796951 |
Anna Beker van Woudenberg1, André Wolterbeek, Lindsey Te Brake, Cor Snel, Aswin Menke, Carina Rubingh, Didima de Groot, Dinant Kroese.
Abstract
Zebrafish embryos were exposed to different organotin compounds during very early development (<100h post fertilization). Morphology, histopathology and swimming activity (in a motor activity test) were the endpoints analyzed. DBTC was, by far, the most embryotoxic compound at all time points and endpoints studied. In fact, we observed a clear concordance between the effects observed in our zebrafish embryo model, and those observed with these compounds in full rodent in vivo studies. All organotin compounds classified as developmental (neuro) toxicants in vivo, were correctly classified in the present assay. Together, our results support the ZET model as a valuable tool for providing biological verification for a grouping and a read-across approach to developmental (neuro) toxicity.Entities:
Keywords: Alternative model; Biological verification; Developmental (neuro) toxicity; Grouping; Organotins; Read across; Zebrafish embryotoxicity test (ZET)
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Year: 2013 PMID: 23796951 DOI: 10.1016/j.reprotox.2013.06.067
Source DB: PubMed Journal: Reprod Toxicol ISSN: 0890-6238 Impact factor: 3.143