State Environmental Protection Key Laboratory of Wetland Ecology and Vegetation Restoration, School of Environment, Northeast Normal University, Changchun, Jilin 130117, PR China.
Department of Physiological Sciences and Center for Environmental and Human Toxicology, University of Florida Genetics Institute, College of Veterinary Medicine, University of Florida, Gainesville, FL 32611, USA.
J Hazard Mater. 2017 Sep 15;338:458-465. doi: 10.1016/j.jhazmat.2017.05.058. Epub 2017 Jun 1.
Chemicals show diverse modes of action (MOAs) in aquatic organisms depending upon acute and chronic toxicity evaluations. Here, toxicity data for Vibrio fischeri involving 52 compounds for acute and chronic toxicity were used to determine the congruence of acute and chronic toxicity for assessing MOAs. Using toxic ratios, most of the compounds categorized into MOAs that included baseline, less inert or reactive compounds with acute toxicity were also categorized as baseline, less inert or reactive compounds with chronic toxicity. However, significantly different toxic effects were observed with acute and chronic toxicity for the reactive and specific-acting compounds. The acute-chronic toxic ratios were smaller and less variable for the baseline and less inert compounds, but were greater and more variable for the reactive and specific-acting compounds. Baseline and less inert compounds share same MOAs, but reactive and specific-acting compounds have different MOAs between acute and chronic toxicity. Bioconcentration processes cannot reach an equilibrium for highly hydrophilic and ionized compounds with short-term exposure, resulting in lower toxicity compared to long-term exposure. Pronounced differences for the antibiotics were not only due to the difference in bioconcentration, but also due to a predicted difference in MOAs during acute and chronic exposures.
化学品在水生生物中表现出多种作用模式(MOAs),具体取决于急性和慢性毒性评估。在这里,使用涉及 52 种化合物的急性和慢性毒性毒性数据,对发光菌进行毒性评估,以确定急性和慢性毒性评估 MOAs 的一致性。使用毒性比,大多数化合物分为具有急性毒性的基线、惰性或反应性较低的化合物,也分为具有慢性毒性的基线、惰性或反应性较低的化合物。然而,对于反应性和特效化合物,急性毒性和慢性毒性的毒性作用明显不同。对于基线和惰性较低的化合物,急性慢性毒性比更小且更稳定,但对于反应性和特效化合物,急性慢性毒性比更大且更不稳定。基线和惰性化合物具有相同的 MOAs,但反应性和特效化合物在急性和慢性毒性之间具有不同的 MOAs。对于具有短期暴露的高亲水性和离子化化合物,生物浓缩过程无法达到平衡,因此与长期暴露相比毒性较低。抗生素的明显差异不仅是由于生物浓缩的差异,也是由于在急性和慢性暴露期间预测的 MOAs 差异。