Department of Veterinary and Biomedical Sciences and The Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University , University Park, PA 16802, United States.
Chem Res Toxicol. 2011 Oct 17;24(10):1601-9. doi: 10.1021/tx200316x. Epub 2011 Sep 28.
The pervasive nature of perfluoroalkyl chemicals in the environment has generated considerable interest for developing new strategies for risk assessment. In experimental animal models, exposure to perfluoroalkyl chemicals can cause developmental toxicity and hepatotoxicity. Peroxisome proliferator-activated receptor-α (PPARα) is required to mediate some but not all of these effects. Since PPARα has a role in mediating some of these effects, and there is some overlap in the type of toxicities elicited by perfluoroalkyl chemicals, it has been suggested that a scaling system analogous to the toxic equivalency factor (TEF) system used for polychlorinated dibenzo-p-dioxins (PCDD), polychlorinated dibenzofurans (PCDF), and polychlorinated biphenyls (PCB) could be used for perfluoroalkyl chemicals. However, evidence suggests that perfluoroalkyl chemicals can activate/interfere with other receptors, and there is reason to suggest the possibility of species differences in the response mediated by different receptors as well as qualitative differences in toxicities elicited by perfluoroalkyl chemicals. These differences and other data gaps preclude the development of a TEF approach for perfluoroalkyl chemicals.
全氟烷基化学品在环境中的普遍存在引发了人们极大的兴趣,促使人们开发新的风险评估策略。在实验动物模型中,接触全氟烷基化学品会导致发育毒性和肝毒性。过氧化物酶体增殖物激活受体-α(PPARα)是介导其中一些但不是全部这些效应所必需的。由于 PPARα 在介导其中一些效应中起作用,并且全氟烷基化学品引起的毒性类型存在一些重叠,因此有人提出,可以使用类似于多氯二苯并对二恶英(PCDD)、多氯二苯并呋喃(PCDF)和多氯联苯(PCB)所用的毒性等效因子(TEF)系统的缩放系统来处理全氟烷基化学品。然而,有证据表明,全氟烷基化学品可以激活/干扰其他受体,并且有理由表明,不同受体介导的反应以及全氟烷基化学品引起的毒性的定性差异可能存在种间差异。这些差异和其他数据空白阻碍了全氟烷基化学品 TEF 方法的开发。