Literature DB >> 25605028

Putative adverse outcome pathways relevant to neurotoxicity.

Anna Bal-Price1, Kevin M Crofton, Magdalini Sachana, Timothy J Shafer, Mamta Behl, Anna Forsby, Alan Hargreaves, Brigitte Landesmann, Pamela J Lein, Jochem Louisse, Florianne Monnet-Tschudi, Alicia Paini, Alexandra Rolaki, André Schrattenholz, Cristina Suñol, Christoph van Thriel, Maurice Whelan, Ellen Fritsche.   

Abstract

The Adverse Outcome Pathway (AOP) framework provides a template that facilitates understanding of complex biological systems and the pathways of toxicity that result in adverse outcomes (AOs). The AOP starts with an molecular initiating event (MIE) in which a chemical interacts with a biological target(s), followed by a sequential series of KEs, which are cellular, anatomical, and/or functional changes in biological processes, that ultimately result in an AO manifest in individual organisms and populations. It has been developed as a tool for a knowledge-based safety assessment that relies on understanding mechanisms of toxicity, rather than simply observing its adverse outcome. A large number of cellular and molecular processes are known to be crucial to proper development and function of the central (CNS) and peripheral nervous systems (PNS). However, there are relatively few examples of well-documented pathways that include causally linked MIEs and KEs that result in adverse outcomes in the CNS or PNS. As a first step in applying the AOP framework to adverse health outcomes associated with exposure to exogenous neurotoxic substances, the EU Reference Laboratory for Alternatives to Animal Testing (EURL ECVAM) organized a workshop (March 2013, Ispra, Italy) to identify potential AOPs relevant to neurotoxic and developmental neurotoxic outcomes. Although the AOPs outlined during the workshop are not fully described, they could serve as a basis for further, more detailed AOP development and evaluation that could be useful to support human health risk assessment in a variety of ways.

Entities:  

Keywords:  adverse outcome pathway; in vitro testing; key events; molecular initiating event; pathways of neurotoxicity; predictive toxicology

Mesh:

Year:  2015        PMID: 25605028      PMCID: PMC5072123          DOI: 10.3109/10408444.2014.981331

Source DB:  PubMed          Journal:  Crit Rev Toxicol        ISSN: 1040-8444            Impact factor:   5.635


  61 in total

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2.  Behavioral toxicology in the 21st century: challenges and opportunities for behavioral scientists. Summary of a symposium presented at the annual meeting of the neurobehavioral teratology society, June, 2009.

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Journal:  Neurotoxicol Teratol       Date:  2010-02-17       Impact factor: 3.763

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6.  In vitro and other alternative approaches to developmental neurotoxicity testing (DNT).

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Journal:  Environ Toxicol Pharmacol       Date:  2005-01-25       Impact factor: 4.860

7.  In vitro developmental neurotoxicity (DNT) testing: relevant models and endpoints.

Authors:  Anna K Bal-Price; Helena T Hogberg; Leonora Buzanska; Petros Lenas; Erwin van Vliet; Thomas Hartung
Journal:  Neurotoxicology       Date:  2009-12-05       Impact factor: 4.294

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Journal:  Environ Health Perspect       Date:  2010-11       Impact factor: 9.031

10.  Meeting report: alternatives for developmental neurotoxicity testing.

Authors:  Pamela Lein; Paul Locke; Alan Goldberg
Journal:  Environ Health Perspect       Date:  2007-01-29       Impact factor: 9.031

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  37 in total

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4.  Differentiating Pathway-Specific From Nonspecific Effects in High-Throughput Toxicity Data: A Foundation for Prioritizing Adverse Outcome Pathway Development.

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Journal:  Toxicol Sci       Date:  2018-06-01       Impact factor: 4.849

5.  Effects of an environmentally-relevant mixture of pyrethroid insecticides on spontaneous activity in primary cortical networks on microelectrode arrays.

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Review 6.  Exposure to Mixtures of Metals and Neurodevelopmental Outcomes: A Multidisciplinary Review Using an Adverse Outcome Pathway Framework.

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7.  Potential frameworks to support evaluation of mechanistic data for developmental neurotoxicity outcomes: A symposium report.

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8.  Stem Cell-Derived Immature Human Dorsal Root Ganglia Neurons to Identify Peripheral Neurotoxicants.

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Journal:  Stem Cells Transl Med       Date:  2016-03-01       Impact factor: 6.940

9.  Phenobarbital use and neurological problems in FMR1 premutation carriers.

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Journal:  Neurotoxicology       Date:  2016-01-21       Impact factor: 4.294

10.  Screening the ToxCast phase II libraries for alterations in network function using cortical neurons grown on multi-well microelectrode array (mwMEA) plates.

Authors:  Jenna D Strickland; Matthew T Martin; Ann M Richard; Keith A Houck; Timothy J Shafer
Journal:  Arch Toxicol       Date:  2017-08-02       Impact factor: 5.153

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