Triclocarban, Triclosan, Bromochlorophene, Chlorophene, and Climbazole Effects on Nuclear Receptors: An in Silico and in Vitro Study

BACKGROUND: Endocrine-disrupting chemicals can interfere with hormonal homeostasis and have adverse effects for both humans and the environment. Their identification is increasingly difficult due to lack of adequate toxicological tests. This difficulty is particularly problematic for cosmetic ingredients, because in vivo testing is now banned completely in the European Union. OBJECTIVES: The aim was to identify candidate preservatives as endocrine disruptors by in silico methods and to confirm endocrine receptors’ activities through nuclear receptors in vitro. METHODS: We screened preservatives listed in Annex V in the European Union Regulation on cosmetic products to predict their binding to nuclear receptors using the Endocrine Disruptome and VirtualToxLab™ version 5.8 in silico tools. Five candidate preservatives were further evaluated for androgen receptor (AR), estrogen receptor ([Formula: see text]), glucocorticoid receptor (GR), and thyroid receptor (TR) agonist and antagonist activities in cell-based luciferase reporter assays in vitro in AR-EcoScreen, [Formula: see text] , MDA-kb2, and GH3.TRE-Luc cell lines. Additionally, assays to test for false positives were used (nonspecific luciferase gene induction and luciferase inhibition). RESULTS: Triclocarban had agonist activity on AR and [Formula: see text] at [Formula: see text] and antagonist activity on GR at [Formula: see text] and TR at [Formula: see text]. Triclosan showed antagonist effects on AR, [Formula: see text] , GR at [Formula: see text] and TR at [Formula: see text] , and bromochlorophene at [Formula: see text] (AR and TR) and at [Formula: see text] ([Formula: see text] and GR). AR antagonist activity of chlorophene was observed [inhibitory concentration at 50% (IC(50)) [Formula: see text]], as for its substantial [Formula: see text] agonist at [Formula: see text] and TR antagonist activity at [Formula: see text]. Climbazole showed AR antagonist ([Formula: see text]), [Formula: see text] agonist at [Formula: see text] , and TR antagonist activity at [Formula: see text]. DISCUSSION: These data support the concerns of regulatory authorities about the endocrine-disrupting potential of preservatives. These data also define the need to further determine their effects on the endocrine system and the need to reassess the risks they pose to human health and the environment. https://doi.org/10.1289/EHP6596