Title: Developmental toxicity, uptake and distribution of sodium chromate assayed by frog embryo teratogenesis assay-Xenopus (FETAX)
Authors: BOSISIO STEFANOFORTANER TORRENT SALVADORBELLINETTO SONIAFARINA MASSIMODEL TORCHIO RICCARDOPRATI MARIANGELAGORNATI ROSALBABERNARDINI GIOVANNISABBIONI ENRICO
Citation: SCIENCE OF THE TOTAL ENVIRONMENT vol. 407 no. 18 p. 5039-5045
Publisher: ELSEVIER SCIENCE BV
Publication Year: 2009
JRC N°: JRC63874
ISSN: 0048-9697
URI: https://www.sciencedirect.com/science/article/pii/S0048969709005233?via%3Dihub
http://publications.jrc.ec.europa.eu/repository/handle/JRC63874
DOI: 10.1016/j.scitotenv.2009.05.047
Type: Articles in periodicals and books
Abstract: The embryotoxicity and teratogenicity of Cr(VI) on the survival and morphology of the anuran Xenopus laevis have been assessed by frog embryo teratogenesis assay-Xenopus (FETAX). The lethal median (LC50) and teratogenic median (TC50) concentration values of Cr(VI) were 890 µM and 260 µM, respectively. The calculated teratogenic index (TI) value was 3.42, suggesting that hexavalent chromium has a teratogenic potential. Malformations of embryos included lifting of the body, coiling of the tail and body oedema. Furthermore, the chromium salt caused significant growth retardation at 25 µM exposure concentrations. The use of radiolabelled 51Cr(VI) allowed the determination of the time course uptake of Cr in Xenopus exposed to concentrations ranging from 0.025 to 500 µM. The evaluation of its distribution into the body (head–abdomen– tail) was evaluated at different exposure times. Chromium is taken up at 24 h by Xenopus embryos for all concentrations tested. At 48 h post fertilization (stage of larva) the amount of Cr accumulated by the two-dayold larva ranged from 0.42 to 580 pg mg-1 wet weight at 0.025 and 500 µMrespectively. These amounts were lower than those at 24 h (2.77 to 11016 pg mg-1 wet weight embryo) reaching values of the same order of magnitude at 120 h (five-days-old larva). Since at 48 h Xenopus development leads to a swimming embryo, the observed uptake at 24 h could be the result of the binding of Cr to jelly coat compounds surrounding the embryo body as confirmed by gel filtration experiments on 51Cr-jelly coat. The interaction of Cr with jelly coat is in agreement with the role of jelly coat in protecting the embryo against pathogen and chemical toxins to ensure fertilization. This work further supports the hypothesis that Cr contamination of surface waters could contribute to explain the reported worldwide depletion of frog population
JRC Directorate:Health, Consumers and Reference Materials

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