A Testing Strategy for the Identification of mammalian Endocrine Disruptors with particular focus on steroids

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A Testing Strategy for the Identification of mammalian Endocrine Disruptors with particular focus on steroids Tzutzuy Ramirez, Robert Landsiedel, Susanne Kolle, Hennicke Kamp, Bennard van Ravenzwaay EUSAAT 1

Our understanding of endocrine disruptors Weybridge 1996: An endocrine disrupter is an exogenous substance that causes adverse health effects in an intact organism, or its progeny, secondary (consequent) to changes in endocrine function. WHO 2002: An endocrine disrupter is an exogenous substance or mixture that alters function(s) of the endocrine system and consequently causes adverse effects in an intact organism, or its progeny, or (sub)populations. Endocrine disruption is potentially a cut-off criterion without any risk assessment 2

1989: The beginning Study case: Vinclozolin Anti-androgenic effects in: prenatal developmental toxicity study: reduced ano-genital distance 2-generation study: a syndrome of changes resulting in a feminization of male rat offspring reduced prostate & seminal vesicle weight and activity hypospadia vaginal pouch delayed / incomplete testicular decent can be explained by several modes of action: 1) Reduction of hormone synthesis 2) Increased breakdown of hormones 3) Receptor block 3

Overview of the Tier-1 EDSP battery In vitro - Androgen receptor (AR) binding -rat prostate cytosol - Estrogen receptor (ER) binding - rat uterine cytosol - Aromatase - Human recombinant aromatase - human estrogen receptor a transcriptional activation in HeLa-9903 line (OECD 455) - Steroidogenesis in H295R line (OECD 456) In vivo - Uterotrophic (rat) (OECD 440) - Hershberger (rat) (OECD 441) - Pubertal female (rat) - Pubertal male (rat) - Amphibian metamorphosis (frog) - Fish short-term reproduction Summarized from EDSP, US-EPA homepage 4

Development and Registration of Agrochemicals: Screening and Selection Years Substances ~140.000 ~25.000 Laboratory 1 ~7.500 Greenhouse >100 Field 2 Toxicology Various crops 3-10 <1 5

An integrated strategy for detection of Endocrine Modes of Action under 3Rs TIER 1 In vitro Refined in vivo Receptor dependent Hormone synthesis Metabolic profiling Assessment for Mammalian Endocrine Activity 6

Tier 1: Yeast Estrogen/ Androgen Screening Assays (YES/YAS) Yeast estrogen/ androgen screening assay Recombinant yeast strains expressing human ER or AR and reporter gene. Agonistic and antagonistic effects measureable Determination of effect by reporter assay 7

Tier 1: Yeast Estrogen/ Androgen Screening Assays (YES/YAS) androgenic activity antiandrogenic activity Positive Control Test subs + PC Test subs Positive Control Test subs + PC Test subs 8

Tier 1: Yeast Estrogen/ Androgen Screening Assays (YES/YAS) (Kolle et al., 2012, RTP) 9

In house validation of the YES/YAS with 105 substances Detection of estrogenic compounds with accuracy of 87%, antiestrogenic with 90%, androgenic with 95% and antiandrogenic with 85%. (Kolle, et al., Toxicol. In Vitro 24(7), 2030-2040). 10

Tier 1: Steroidogenesis assay OECD TG 456 and OPPTS 890.1550 The objective of the steroidogenic screen assay is to detect any substance that would disrupt estrogen and/or androgen gonadal steroid hormone production. Summarized from EDSP, US-EPA homepage OECD guideline 456 11

Tier 1: Effects of vinclozolin on the levels of estradiol and testosterone Estradiol Testosterone 12

An integrated strategy for detection of Endocrine Modes of Action under 3Rs TIER 2 In vitro Refined in vivo Receptor dependent Hormone synthesis Metabolic profiling Assessment for Mammalian Endocrine Activity 13

Tier 2: In vivo 28 day study combined with metabolomics analysis Confirmation of in vitro findings (potency / NOAEL) Detection of compounds that only act in vivo (e.g. metabolism specific) OECD 407 (28 day rat study) Estrus cycle analysis Pathology of endocrine organs Metabolome analysis 06/09/2012 14

Analysis of effects of 14 compounds tested in vitro and in vivo Of the nine known EDCs all substances were determined to exert receptor mediated and/or biosynthesis related mechanisms. The effects were confirmed by in vivo metabolome analysis in the OECD TG 407 study. (Kolle et al., 2012, RTP) 15

Assessment of mammalian endocrine effects using a combination of in vitro assays and in vivo assays (Kolle et al., 2012, RTP) 16

Tiered Testing for Identification of Endocrine Disruption In vitro Refined in vivo Receptor dependent Hormone synthesis Metabolic profiling Retrospective analysis of in house data showed that with the proposed testing strategy additional in vivo studies Hershberger assay (OECD 441), uterotrophic assay (OECD 440), pubertal assays are not needed. 17

Thank you Laboratory of Development of Alternative Methods Laboratory of Applied Alternative Methods BASF Experimental Toxicology and Ecology Metanomics GmbH 18