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      In vitro or not in vitro: a short journey through a long history

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          Abstract

          The aim of ecotoxicology is to study toxic effects on constituents of ecosystems, with the protection goal being populations and communities rather than individual organisms. In this ecosystem perspective, the use of in vitro methodologies measuring cellular and subcellular endpoints at a first glance appears to be odd. Nevertheless, more recently in vitro approaches gained momentum in ecotoxicology. In this article, we will discuss important application domains of in vitro methods in ecotoxicology. One area is the use of in vitro assays to replace, reduce, and refine (3R) in vivo tests. Research in this field has focused mainly on the use of in vitro cytotoxicity assays with fish cells as non-animal alternative to the in vivo lethality test with fish and on in vitro biotransformation assays as part of an alternative testing strategy for bioaccumulation testing with fish. Lessons learned from this research include the importance of a critical evaluation of the sensitivity, specificity and exposure conditions of in vitro assays, as well as the availability of appropriate in vitro-in vivo extrapolation models. In addition to this classical 3R application, other application domains of in vitro assays in ecotoxicology include the screening and prioritization of chemical hazards, the categorization of chemicals according to their modes of action and the provision of mechanistic information for the pathway-based prediction of adverse outcomes. The applications discussed in this essay may highlight the potential of in vitro technologies to enhance the environmental hazard assessment of single chemicals and complex mixtures at a reduced need of animal testing.

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          A review of bioconcentration factor (BCF) and bioaccumulation factor (BAF) assessments for organic chemicals in aquatic organisms

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            Toxicity determined in vitro by morphological alterations and neutral red absorption

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              In vitro profiling of the endocrine-disrupting potency of brominated flame retardants.

              Over the last few years, increasing evidence has become available that some brominated flame retardants (BFRs) may have endocrine-disrupting (ED) potencies. The goal of the current study was to perform a systematic in vitro screening of the ED potencies of BFRs (1) to elucidate possible modes of action of BFRs in man and wildlife and (2) to classify BFRs with similar profiles of ED potencies. A test set of 27 individual BFRs were selected, consisting of 19 polybrominated diphenyl ether congeners, tetrabromobisphenol-A, hexabromocyclododecane, 2,4,6-tribromophenol, ortho-hydroxylated brominated diphenyl ether 47, and tetrabromobisphenol-A-bis(2,3)dibromopropyl ether. All BFRs were tested for their potency to interact with the arylhydrocarbon receptor, androgen receptor (AR), progesterone receptor (PR), and estrogen receptor. In addition, all BFRs were tested for their potency to inhibit estradiol (sulfation by estradiol sulfotransferase (E2SULT), to interfere with thyroid hormone 3,3',5-triiodothyronine (T3)-mediated cell proliferation, and to compete with T3-precursor thyroxine for binding to the plasma transport protein transthyretin (TTR). The results of the in vitro screening indicated that BFRs have ED potencies, some of which had not or only marginally been described before (AR antagonism, PR antagonism, E2SULT inhibition, and potentiation of T3-mediated effects). For some BFRs, the potency to induce AR antagonism, E2SULT inhibition, and TTR competition was higher than for natural ligands or clinical drugs used as positive controls. Based on their similarity in ED profiles, BFRs were classified into five different clusters. These findings support further investigation of the potential ED effects of these environmentally relevant BFRs in man and wildlife.
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                Author and article information

                Contributors
                kristina.rehberger@vetsuisse.unibe.ch
                christian.kropf@vetsuisse.unibe.ch
                helmut.segner@vetsuisse.unibe.ch
                Journal
                Environ Sci Eur
                Environ Sci Eur
                Environmental Sciences Europe
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                2190-4707
                2190-4715
                26 June 2018
                26 June 2018
                2018
                : 30
                : 1
                : 23
                Affiliations
                ISNI 0000 0001 0726 5157, GRID grid.5734.5, Centre for Fish and Wildlife Health, Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, , University of Bern, ; P O Box, 3001 Bern, Switzerland
                Author information
                http://orcid.org/0000-0003-4071-3884
                http://orcid.org/0000-0002-2104-9730
                http://orcid.org/0000-0002-1783-1295
                Article
                151
                10.1186/s12302-018-0151-3
                6018605
                fb101ceb-1e00-486b-b85e-b819cf6bd62e
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 14 March 2018
                : 6 June 2018
                Funding
                Funded by: EU project SOLUTIONS
                Award ID: 603437
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Author(s) 2018

                cytotoxicity,biotransformation,bioaccumulation,hazard profiling,in vivo,risk assessment,toxicity pathways,prioritization,screening,high-throughput

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