Guarino A M
Environ Health Perspect. 1987 Apr;71:17-24. doi: 10.1289/ehp.877117.
The large body of literature and techniques generated by mammalian toxicity studies provides a conceptual and technical framework within which the absorption, fate, and disposition of xenobiotics in aquatic organisms can be studied. This review emphasizes the similarities and differences between mammalian and aquatic systems, e.g., lung vs. gill as site of absorption and toxicity. These must be taken into consideration when designing aquatic toxicity studies. Studies of phenol red in dogfish shark as an example show physiologic-based pharmacokinetic modeling to be a useful tool for investigating and eventually predicting species differences in xenobiotic disposition and drug differences within the same species. This discussion demonstrates that both laboratory and modeling procedures are now available to carry out sophisticated studies of xenobiotic fate and disposition in fish. Such studies are needed to pinpoint sites and mechanisms of pollutant toxicity in aquatic organisms.
哺乳动物毒性研究产生的大量文献和技术提供了一个概念和技术框架,在此框架内可以研究水生生物中外源化学物质的吸收、归宿和处置。本综述强调了哺乳动物和水生系统之间的异同,例如作为吸收和毒性部位的肺与鳃。在设计水生毒性研究时必须考虑这些因素。以角鲨体内的酚红研究为例,表明基于生理学的药代动力学建模是研究并最终预测同一物种中外源化学物质处置的物种差异和药物差异的有用工具。该讨论表明,现在既有实验室程序也有建模程序可用于开展对鱼类中外源化学物质归宿和处置的深入研究。需要此类研究来确定水生生物中污染物毒性的部位和机制。