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               <dc:title>Assessment of Developmental Delay in the Zebrafish embryo Teratogenicity Assay</dc:title>
               <dc:creator>Teixidó Condomines, Elisabet</dc:creator>
               <dc:creator>Piqué Benages, Maria Esther</dc:creator>
               <dc:creator>Gómez Catalán, Jesús</dc:creator>
               <dc:creator>Llobet Mallafré, Joan M. (Joan Maria)</dc:creator>
               <dc:subject>Enzimologia</dc:subject>
               <dc:subject>Embriologia</dc:subject>
               <dc:subject>Metabolisme</dc:subject>
               <dc:subject>Acetilcolinesterasa</dc:subject>
               <dc:subject>Nanisme</dc:subject>
               <dc:subject>Malformacions</dc:subject>
               <dc:subject>Peix zebra</dc:subject>
               <dc:subject>Toxicologia</dc:subject>
               <dc:subject>Enzymology</dc:subject>
               <dc:subject>Embryology</dc:subject>
               <dc:subject>Metabolism</dc:subject>
               <dc:subject>Acetylcholinesterase</dc:subject>
               <dc:subject>Dwarfism</dc:subject>
               <dc:subject>Human abnormalities</dc:subject>
               <dc:subject>Zebra danio</dc:subject>
               <dc:subject>Toxicology</dc:subject>
               <dc:description>In this study we analyzed some aspects of the assessment of developmental delay in the zebrafish embryotoxicity/teratogenicity test and explored the suitability of acetylcholinesterase (AChE) activity as a biochemical marker and as a higher throughput alternative to morphological endpoints such as head-trunk angle, tail length and morphological score. Embryos were exposed from 4 to 52 h post-fertilization (hpf) to a selection of known embryotoxic/teratogen compounds (valproic acid, retinoic acid, caffeine, sodium salicylate, glucose, hydroxyurea, methoxyacetic acid, boric acid and paraoxon-methyl) over a concentration range. They were evaluated for AChE activity, head-trunk angle, tail length and several qualitative parameters integrated in a morphological score. In general, the different patterns of the concentration-response curves allowed distinguishing between chemicals that produced growth retardation (valproic and methoxyacetic acid) and chemicals that produced non-growth-delay related malformations. An acceptable correlation between the morphological score, AChE activity and head-trunk angle as markers of developmental delay was observed, being AChE activity particularly sensitive to detect delay in the absence of malformations.</dc:description>
               <dc:date>2020-06-12T07:18:48Z</dc:date>
               <dc:date>2020-06-12T07:18:48Z</dc:date>
               <dc:date>2013-02-27</dc:date>
               <dc:date>2020-06-12T07:18:48Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
               <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1016/j.tiv.2012.07.010</dc:relation>
               <dc:relation>Toxicology in Vitro, 2013, vol. 27, num. 1, p. 469-478</dc:relation>
               <dc:relation>https://doi.org/10.1016/j.tiv.2012.07.010</dc:relation>
               <dc:rights>(c) Elsevier Ltd, 2013</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Elsevier Ltd</dc:publisher>
               <dc:source>Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)</dc:source>
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