Grouping of endocrine disrupting chemicals for mixture risk assessment – Evidence from a rat study. (September 2020)

• Record Type: Journal Article
• Authors: Christiansen, Sofie; Axelstad, Marta; Scholze, Martin; Johansson, Hanna K.L.; Hass, Ulla; Mandrup, Karen; Frandsen, Henrik Lauritz; Frederiksen, Hanne; Isling, Louise Krag; Boberg, Julie
• Is Part Of: Environment international. Volume 142(2020)
• Publication Date: 2020-09
• Subjects: Mixture risk assessment -- Endocrine disruptive chemicals -- EDC -- Adverse outcome pathway; Environmental protection -- Periodicals; Environmental health -- Periodicals; Environmental monitoring -- Periodicals; Environmental Monitoring -- Periodicals; Environnement -- Protection -- Périodiques; Hygiène du milieu -- Périodiques; Environnement -- Surveillance -- Périodiques; Environmental health; Environmental monitoring; Environmental protection; Periodicals; 333.705
• DOI: 10.1016/j.envint.2020.105870
• Languages: English
• ISSNs: 0160-4120

Abstract

Highlights: Grouping of chemicals for risk assessment should be based on shared health outcomes. Adverse Outcome Pathway can provide important guidance to mixture risk assessment. Several modes of action can converge into a common adverse health outcome. Abstract: Exposure to mixtures of endocrine disrupting chemicals may contribute to the rising incidence of hormone-related diseases in humans. Real-life mixtures are complex, comprised of chemicals with mixed modes of action, and essential knowledge is often lacking on how to group such chemicals into cumulative assessment groups, which is an essential prerequisite to conduct a chemical mixture risk assessment. We investigated if mixtures of chemicals with diverse endocrine modes of action can cause mixture effects on hormone sensitive endpoints in developing and adult rat offspring after perinatal exposure. Wistar rats were exposed during pregnancy and lactation simultaneously to either bisphenol A and butylparaben (Emix), diethylhexyl phthalate and procymidone (Amix), or a mixture of all four substances (Totalmix). In male offspring, the anogenital distance was significantly reduced and nipple retention increased in animals exposed to Amix and Totalmix, and the mixture effects were well approximated by the dose addition model. The combination of Amix and Emix responded with more marked changes on these and other endocrine-sensitive endpoints than each binary mixture on its own. Sperm counts were reduced by all exposures. These experimental outcomes suggest that the grouping of chemicals for mixture risk assessment should be based on common health outcomes rather than only similar modes or mechanisms of action. Mechanistic-based approaches such as the concept of Adverse Outcome Pathway (AOP) can provide important guidance if both the information on shared target tissues and the information on shared mode/mechanism of action are taken into account.