Song You, Evenseth Linn Mari, Iguchi Taisen, Tollefsen Knut Erik
a Norwegian Institute for Water Research (NIVA) , Gaustadalléen , Oslo , Norway.
b Department of Medical Biology , Faculty of Health Sciences, University of Tromsø-The Arctic University of Norway , Tromsø , Norway.
J Toxicol Environ Health A. 2017;80(16-18):954-962. doi: 10.1080/15287394.2017.1352215. Epub 2017 Aug 29.
During arthropod molting, the old exoskeleton is degraded and recycled by the molting fluid. Chitobiase, a major chitinolytic enzyme in the molting fluid, has been widely used as a biomarker to indicate endocrine disruption of molting in arthropods under environmental stress. Although release of chitobiase was extensively studied in organisms exposed to molting-inhibiting chemicals, enzymic association with molting and response of the molting hormone receptor, ecdysone receptor (EcR), is not well understood. The present study was therefore conducted to identify potential linkages between release of chitobiase, molting frequency, and EcR activation in a freshwater crustacean Daphnia magna after short-term (96 hr) exposure to endogenous molting hormone 20-hydroxyecdysone (20E). A suite of bioassays was used for this purpose, including the chitobiase activity, molting frequency, viability, and in vitro EcR activation. Effect concentrations were compared between different assays analyzed. Results showed that exposure to 20E reduced chitobiase release and molting frequency in a concentration-dependent manner. Exposure to as low as 250 nM 20E significantly decreased release of chitobiase after 72 hr exposure, whereas adverse effects on molting frequency and incomplete molting-associated mortality required higher 20E exposure concentrations. The EcR reporter assay further demonstrated that as low as 100 nM 20E may activate EcR in vitro. Data suggest that release of chitobiase may be employed as a sensitive indicator of potential molting disruption in crustaceans after exposure to EcR agonists such as 20E.
在节肢动物蜕皮过程中,旧的外骨骼会被蜕皮液降解并循环利用。几丁质酶是蜕皮液中的一种主要几丁质分解酶,已被广泛用作生物标志物,以指示环境压力下节肢动物蜕皮的内分泌紊乱。尽管在接触蜕皮抑制化学物质的生物体中对几丁质酶的释放进行了广泛研究,但关于其与蜕皮的酶学关联以及蜕皮激素受体——蜕皮激素受体(EcR)的反应,人们还了解得不够透彻。因此,本研究旨在确定在淡水甲壳动物大型溞短期(96小时)暴露于内源性蜕皮激素20-羟基蜕皮酮(20E)后,几丁质酶释放、蜕皮频率和EcR激活之间的潜在联系。为此使用了一系列生物测定方法,包括几丁质酶活性、蜕皮频率、活力和体外EcR激活。对不同分析测定的效应浓度进行了比较。结果表明,暴露于20E会以浓度依赖的方式降低几丁质酶释放和蜕皮频率。暴露于低至250 nM的20E 72小时后,几丁质酶释放显著降低,而对蜕皮频率和与不完全蜕皮相关的死亡率的不利影响则需要更高的20E暴露浓度。EcR报告基因测定进一步表明,低至100 nM的20E可能在体外激活EcR。数据表明,几丁质酶的释放可能被用作甲壳动物在暴露于诸如20E等EcR激动剂后潜在蜕皮破坏的敏感指标。