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      The Extended Amphibian Metamorphosis Assay: A Thyroid‐Specific and Less Animal‐Intensive Alternative to the Larval Amphibian Growth and Development Assay

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          Abstract

          The amphibian metamorphosis assay (AMA; US Environmental Protection Agency [USEPA] test guideline 890.1100 and Organisation for Economic Co‐Operation and Development test guideline 231) has been used for more than a decade to assess the potential thyroid‐mediated endocrine activity of chemicals. In 2013, in the context of the Endocrine Disruptor Screening Program of the USEPA, a Scientific Advisory Panel reviewed the results from 18 studies and recommended changes to the AMA test guideline, including a modification to a fixed‐stage design rather than a fixed‐time (i.e., 21‐d) design. We describe an extended test design for the AMA (or EAMA) that includes thyroid histopathology and time to metamorphosis (Nieuwkoop–Faber [NF] stage 62), to address both the issues with the fixed‐time design and the specific question of thyroid‐mediated adversity in a shorter assay than the larval amphibian growth and development assay (LAGDA; Organisation for Economic Co‐Operation and Development test guideline 241), using fewer animals and resources. A demonstration study was conducted with the EAMA (up to NF stage 58) using sodium perchlorate. Data analyses and interpretation of the fixed‐stage design of the EAMA are more straightforward than the fixed‐time design because the fixed‐stage design avoids confounded morphometric measurements and thyroid histopathology caused by varying developmental stages at test termination. It also results in greater statistical power to detect metamorphic delays than the fixed‐time design. By preferentially extending the AMA to NF stage 62, suitable data can be produced to evaluate thyroid‐mediated adversity and preclude the need to perform a LAGDA for thyroid mode of action analysis. The LAGDA remains of further interest should investigations of longer term effects related to sexual development modulated though the hypothalamus pituitary gonadal axis be necessary. However, reproduction assessment or life cycle testing is currently not addressed in the LAGDA study design. This is better addressed by higher tier studies in fish, which should then include specific thyroid‐related endpoints. Environ Toxicol Chem 2021;40:2135–2144. © 2021 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.

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          Guidance for the identification of endocrine disruptors in the context of Regulations ( EU ) No 528/2012 and ( EC ) No 1107/2009

          Abstract This Guidance describes how to perform hazard identification for endocrine‐disrupting properties by following the scientific criteria which are outlined in Commission Delegated Regulation (EU) 2017/2100 and Commission Regulation (EU) 2018/605 for biocidal products and plant protection products, respectively.
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            R: A language and environment for statistical computing

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              Effects of estradiol, benzophenone-2 and benzophenone-3 on the expression pattern of the estrogen receptors (ER) alpha and beta, the estrogen receptor-related receptor 1 (ERR1) and the aryl hydrocarbon receptor (AhR) in adult ovariectomized rats.

              The estrogen receptors (ERs) are members of a super family of ligand-activated transcription factors mediating estrogenic responses. A close functional kinship was found for the structurally related estrogen receptor-related receptor1 (ERR1), a constitutively active transcription factor. The aryl hydrocarbon receptor (AhR) mediates the toxic and estrogenic effects of a wide variety of environmental contaminants and industrial pollutants. Both the ERR1 and the AhR are known to modulate the ER's signalling pathways in multiple ways. Organic chemicals with a certain structural relationship to steroid hormones often induce a tissue- or cell-specific variety of responses distinct from estrogenic responses and this may involve ERR1 and AhR. The UV-screens benzophenone-2 and benzophenone-3 (BP2, BP3), structurally related to known steroid receptor ligands, are used in cosmetics and plastics to improve product stability and durability. Both BP2 and BP3 were shown to exert uterotrophic effects and BP2 was shown to bind to the estrogen receptors. Whether such effects are also exerted in other organs is unknown. Therefore, an approach to a multi-organic risk assessment for these substances was made by measuring the gene-expression of the four mentioned receptors in the pituitary, the uterus and the thyroid after a five-day treatment in comparison to estradiol. Though BP2 seems to exert an estrogen-like effect while BP3 does not, there are regulatory effects on receptor expression for both substances that indicate a kind of endocrine disruption that is not assessed by "classical" estrogenic markers.

                Author and article information

                Contributors
                laurent.lagadic@bayer.com
                Journal
                Environ Toxicol Chem
                Environ Toxicol Chem
                10.1002/(ISSN)1552-8618
                ETC
                Environmental Toxicology and Chemistry
                John Wiley and Sons Inc. (Hoboken )
                0730-7268
                1552-8618
                18 June 2021
                August 2021
                : 40
                : 8 ( doiID: 10.1002/etc.v40.8 )
                : 2135-2144
                Affiliations
                [ 1 ] Bayer U.S. LLC, Crop Science Environmental Effects and Risk Assessment Cary North Carolina USA
                [ 2 ] BASF Corporation, Agricultural Solutions–Ecotoxicology Research Triangle Park North Carolina USA
                [ 3 ] BASF SE Agricultural Solutions–Ecotoxicology Limburgerhof Germany
                [ 4 ] Shell International B.V. Shell Health The Hague The Netherlands
                [ 5 ] Bayer U.S. LLC, Crop Science Environmental Effects and Risk Assessment Chesterfield Missouri USA
                [ 6 ] SynTech Research, Stilwell Kansas USA
                [ 7 ] National Centre for the Replacement, Refinement, & Reduction of Animals in Research London United Kingdom
                [ 8 ] Bayer AG, Research and Development, Crop Science, Environmental Safety Monheim am Rhein Germany
                Author notes
                [*] [* ] Address correspondence to laurent.lagadic@ 123456bayer.com

                Author information
                http://orcid.org/0000-0002-5191-4158
                Article
                ETC5078
                10.1002/etc.5078
                8362105
                33939850
                5923bc1b-1c93-42a7-841e-00cb8fa870c1
                © 2021 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 13 March 2021
                : 03 February 2021
                : 21 April 2021
                Page count
                Figures: 1, Tables: 4, Pages: 10, Words: 8622
                Categories
                Critical Perspectives
                Critical Perspectives
                Custom metadata
                2.0
                August 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.5 mode:remove_FC converted:13.08.2021

                Environmental chemistry
                Environmental chemistry

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