Comparison of toxicity values across zebrafish early life stages and mammalian studies: Implications for chemical testing

被引:97
作者
Ducharme, Nicole A. [1 ]
Reif, David M. [3 ]
Gustafsson, Jan-Ake [1 ,2 ]
Bondesson, Maria [1 ]
机构
[1] Univ Houston, Dept Biol & Biochem, Ctr Nucl Receptors & Cell Signaling, Houston, TX 77204 USA
[2] Karolinska Inst, Dept Biosci & Nutr, S-14183 Huddinge, Sweden
[3] N Carolina State Univ, Dept Biol Sci, Bioinformat Res Ctr, Raleigh, NC 27695 USA
基金
美国国家环境保护局;
关键词
Meta-analysis; Toxicity; Teratogen; Zebrafish; Human exposure; DEVELOPMENTAL TOXICITY; EMBRYOTOXICITY TEST; BISPHENOL-A; MODEL; EXPOSURE; TERATOGENICITY; RECEPTOR; ASSAY;
D O I
10.1016/j.reprotox.2014.09.005
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
With the high cost and slow pace of toxicity testing in mammals, the vertebrate zebrafish has become a tractable model organism for high throughput toxicity testing. We present here a meta-analysis of 600 chemicals tested for toxicity in zebrafish embryos and larvae. Nineteen aggregated and 57 individual toxicity endpoints were recorded from published studies yielding 2695 unique data points. These data points were compared to lethality and reproductive toxicology endpoints analyzed in rodents and rabbits and to exposure values for humans. We show that although many zebrafish endpoints did not correlate to rodent or rabbit acute toxicity data, zebrafish could be used to accurately predict relative acute toxicity through the rat inhalation, rabbit dermal, and rat oral exposure routes. Ranking of the chemicals based on toxicity and teratogenicity in zebrafish, as well as human exposure levels, revealed that 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), benzo(a)pyrene, and chlorpyrifos ranked in the top nine of all chemicals for these three categories, and as such should be considered high priority chemicals for testing in higher vertebrates. (C) 2014 Elsevier All rights reserved.
引用
收藏
页码:3 / 10
页数:8
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