13
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Putative adverse outcome pathways for female reproductive disorders to improve testing and regulation of chemicals

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Modern living challenges female reproductive health. We are witnessing a rise in reproductive disorders and drop in birth rates across the world. The reasons for these manifestations are multifaceted and most likely include continuous exposure to an ever-increasing number of chemicals. The cause–effect relationships between chemical exposure and female reproductive disorders, however, have proven problematic to determine. This has made it difficult to assess the risks chemical exposures pose to a woman’s reproductive development and function. To address this challenge, this review uses the adverse outcome pathway (AOP) concept to summarize current knowledge about how chemical exposure can affect female reproductive health. We have a special focus on effects on the ovaries, since they are essential for lifelong reproductive health in women, being the source of both oocytes and several reproductive hormones, including sex steroids. The AOP framework is widely accepted as a new tool for toxicological safety assessment that enables better use of mechanistic knowledge for regulatory purposes. AOPs equip assessors and regulators with a pragmatic network of linear cause–effect relationships, enabling the use of a wider range of test method data in chemical risk assessment and regulation. Based on current knowledge, we propose ten putative AOPs relevant for female reproductive disorders that can be further elaborated and potentially be included in the AOPwiki. This effort is an important step towards better safeguarding the reproductive health of all girls and women.

          Related collections

          Most cited references136

          • Record: found
          • Abstract: found
          • Article: not found

          Recombination, Pairing, and Synapsis of Homologs during Meiosis.

          Recombination is a prominent feature of meiosis in which it plays an important role in increasing genetic diversity during inheritance. Additionally, in most organisms, recombination also plays mechanical roles in chromosomal processes, most notably to mediate pairing of homologous chromosomes during prophase and, ultimately, to ensure regular segregation of homologous chromosomes when they separate at the first meiotic division. Recombinational interactions are also subject to important spatial patterning at both early and late stages. Recombination-mediated processes occur in physical and functional linkage with meiotic axial chromosome structure, with interplay in both directions, before, during, and after formation and dissolution of the synaptonemal complex (SC), a highly conserved meiosis-specific structure that links homolog axes along their lengths. These diverse processes also are integrated with recombination-independent interactions between homologous chromosomes, nonhomology-based chromosome couplings/clusterings, and diverse types of chromosome movement. This review provides an overview of these diverse processes and their interrelationships.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Clinical practice. Primary ovarian insufficiency.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Retinoid signaling determines germ cell fate in mice.

              Germ cells in the mouse embryo can develop as oocytes or spermatogonia, depending on molecular cues that have not been identified. We found that retinoic acid, produced by mesonephroi of both sexes, causes germ cells in the ovary to enter meiosis and initiate oogenesis. Meiosis is retarded in the fetal testis by the action of the retinoid-degrading enzyme CYP26B1, ultimately leading to spermatogenesis. In testes of Cyp26b1-knockout mouse embryos, germ cells enter meiosis precociously, as if in a normal ovary. Thus, precise regulation of retinoid levels during fetal gonad development provides the molecular control mechanism that specifies germ cell fate.
                Bookmark

                Author and article information

                Contributors
                tesv@food.dtu.dk
                Journal
                Arch Toxicol
                Arch. Toxicol
                Archives of Toxicology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0340-5761
                1432-0738
                7 July 2020
                7 July 2020
                2020
                : 94
                : 10
                : 3359-3379
                Affiliations
                [1 ]GRID grid.5170.3, ISNI 0000 0001 2181 8870, Division of Diet, Disease Prevention and Toxicology, National Food Institute, , Technical University of Denmark, ; 2800 Kongens Lyngby, Denmark
                [2 ]GRID grid.24381.3c, ISNI 0000 0000 9241 5705, Department of Clinical Science, Intervention and Technology, , Karolinska Institutet and Karolinska University Hospital, ; 14186 Stockholm, Sweden
                [3 ]GRID grid.12380.38, ISNI 0000 0004 1754 9227, Department Environment and Health, , Vrije Universiteit Amsterdam, ; De Boelelaan 1085, 1081 HV Amsterdam, The Netherlands
                [4 ]GRID grid.4861.b, ISNI 0000 0001 0805 7253, Neuroendocrinology Unit, GIGA Neurosciences, , University of Liège, ; Sart-Tilman, 4000 Liège, Belgium
                [5 ]GRID grid.12380.38, ISNI 0000 0004 1754 9227, Faculty of Science, , Vrije Universiteit Amsterdam, ; 1081 HV Amsterdam, The Netherlands
                [6 ]GRID grid.487355.8, Competence Centre on Health Technologies, ; Tartu, Estonia
                [7 ]GRID grid.6988.f, ISNI 0000000110107715, Department of Chemistry and Biotechnology, School of Science, , Tallinn University of Technology, ; Tallinn, Estonia
                [8 ]GRID grid.4777.3, ISNI 0000 0004 0374 7521, Institute for Global Food Security, School of Biological Sciences, , Queen’s University Belfast, ; Belfast, BT9 5DL Northern Ireland UK
                [9 ]GRID grid.410368.8, ISNI 0000 0001 2191 9284, Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement et Travail) UMR_S 1085, , University Rennes, ; 35000 Rennes, France
                [10 ]GRID grid.10939.32, ISNI 0000 0001 0943 7661, Department of Obstetrics and Gynaecology, Institute of Clinical Medicine, , University of Tartu, ; Tartu, Estonia
                [11 ]Department of Obstetrics and Gynecology, University of Helsinki, Helsinki University Hospital, Helsinki, Finland
                [12 ]GRID grid.7107.1, ISNI 0000 0004 1936 7291, Institute of Medical Sciences, , University of Aberdeen, ; Foresterhill, Aberdeen, AB25 2ZD UK
                [13 ]GRID grid.411374.4, ISNI 0000 0000 8607 6858, Department of Pediatrics, , CHU de Liège, ; Rue de Gaillarmont 600, 4032 Liège, Belgium
                Author information
                http://orcid.org/0000-0001-9526-6837
                http://orcid.org/0000-0001-8458-0855
                http://orcid.org/0000-0002-3838-9731
                http://orcid.org/0000-0003-2255-1201
                http://orcid.org/0000-0003-2936-6682
                http://orcid.org/0000-0003-2357-5096
                http://orcid.org/0000-0002-0503-9292
                http://orcid.org/0000-0002-6266-1248
                http://orcid.org/0000-0003-1927-9016
                http://orcid.org/0000-0002-6518-2517
                http://orcid.org/0000-0003-0566-4124
                http://orcid.org/0000-0002-1251-8160
                http://orcid.org/0000-0001-6986-5991
                http://orcid.org/0000-0002-4121-9354
                http://orcid.org/0000-0002-4831-9075
                http://orcid.org/0000-0001-6553-3260
                http://orcid.org/0000-0002-4292-846X
                http://orcid.org/0000-0003-4650-7651
                Article
                2834
                10.1007/s00204-020-02834-y
                7502037
                32638039
                a620d2f1-e9ff-4024-87b0-3a751d2ae4d6
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 31 March 2020
                : 30 June 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100010661, Horizon 2020 Framework Programme;
                Award ID: 825100
                Award Recipient :
                Categories
                Review Article
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2020

                Toxicology
                ovary,reproduction,adverse outcome pathway,aop,ovarian dysgenesis syndrome,ods,endocrine-disrupting chemicals,edc

                Comments

                Comment on this article