Cavallin Jenna E, Ankley Gerald T, Blackwell Brett R, Blanksma Chad A, Fay Kellie A, Jensen Kathleen M, Kahl Michael D, Knapen Dries, Kosian Patricia A, Poole Shane T, Randolph Eric C, Schroeder Anthony L, Vergauwen Lucia, Villeneuve Daniel L
Badger Technical Services, Mid-Continent Ecology Division, US Environmental Protection Agency, Duluth, Minnesota, USA.
Mid-Continent Ecology Division, US Environmental Protection Agency, Duluth, Minnesota, USA.
Environ Toxicol Chem. 2017 Nov;36(11):2942-2952. doi: 10.1002/etc.3855. Epub 2017 Jun 28.
Inflation of the posterior and/or anterior swim bladder is a process previously demonstrated to be regulated by thyroid hormones. We investigated whether inhibition of deiodinases, which convert thyroxine (T4) to the more biologically active form, 3,5,3'-triiodothyronine (T3), would impact swim bladder inflation. Two experiments were conducted using a model deiodinase inhibitor, iopanoic acid (IOP). First, fathead minnow embryos were exposed to 0.6, 1.9, or 6.0 mg/L or control water until 6 d postfertilization (dpf), at which time posterior swim bladder inflation was assessed. To examine anterior swim bladder inflation, a second study was conducted with 6-dpf larvae exposed to the same IOP concentrations until 21 dpf. Fish from both studies were sampled for T4/T3 measurements and gene transcription analyses. Incidence and length of inflated posterior swim bladders were significantly reduced in the 6.0 mg/L treatment at 6 dpf. Incidence of inflation and length of anterior swim bladder were significantly reduced in all IOP treatments at 14 dpf, but inflation recovered by 18 dpf. Throughout the larval study, whole-body T4 concentrations increased and T3 concentrations decreased in all IOP treatments. Consistent with hypothesized compensatory responses, deiodinase-2 messenger ribonucleic acid (mRNA) was up-regulated in the larval study, and thyroperoxidase mRNA was down-regulated in all IOP treatments in both studies. These results support the hypothesized adverse outcome pathways linking inhibition of deiodinase activity to impaired swim bladder inflation. Environ Toxicol Chem 2017;36:2942-2952. Published 2017 Wiley Periodicals Inc. on behalf of SETAC. This article is a US government work and, as such, is in the public domain in the United States of America.
后和/或前鳔充气是一个先前已证明受甲状腺激素调节的过程。我们研究了抑制将甲状腺素(T4)转化为生物活性更强的形式3,5,3'-三碘甲状腺原氨酸(T3)的脱碘酶是否会影响鳔充气。使用模型脱碘酶抑制剂碘番酸(IOP)进行了两项实验。首先,将黑头软口鲦胚胎暴露于0.6、1.9或6.0mg/L的IOP或对照水中,直至受精后6天(dpf),此时评估后鳔充气情况。为了检查前鳔充气情况,进行了第二项研究,将6 dpf的幼虫暴露于相同的IOP浓度下,直至21 dpf。对两项研究中的鱼进行采样,以测量T4/T3并进行基因转录分析。在6 dpf时,6.0mg/L处理组中后鳔充气的发生率和长度显著降低。在14 dpf时,所有IOP处理组中前鳔充气的发生率和长度均显著降低,但在18 dpf时充气情况恢复。在整个幼虫研究中,所有IOP处理组的全身T4浓度均升高,T3浓度均降低。与假设的代偿反应一致,在幼虫研究中脱碘酶-2信使核糖核酸(mRNA)上调,在两项研究的所有IOP处理组中甲状腺过氧化物酶mRNA均下调。这些结果支持了假设的不良结局途径,即脱碘酶活性抑制与鳔充气受损相关。《环境毒理学与化学》2017年;36:2942 - 2952。2017年由威利期刊公司代表SETAC出版。本文是美国政府工作成果,因此在美国属于公共领域。