Defining and modeling known adverse outcome pathways: Domoic acid and neuronal signaling as a case study

Karen Watanabe-Sailor, Melvin E. Andersen, Niladri Basu, Michael J. Carvan, Kevin M. Crofton, Kerensa A. King, Cristina Suñol, Evelyn Tiffany-Castiglioni, Irvin R. Schultz

Research output: Contribution to journalArticle

48 Citations (Scopus)

Abstract

An adverse outcome pathway (AOP) is a sequence of key events from a molecular-level initiating event and an ensuing cascade of steps to an adverse outcome with population-level significance. To implement a predictive strategy for ecotoxicology, the multiscale nature of an AOP requires computational models to link salient processes (e.g., in chemical uptake, toxicokinetics, toxicodynamics, and population dynamics). A case study with domoic acid was used to demonstrate strategies and enable generic recommendations for developing computational models in an effort to move toward a toxicity testing paradigm focused on toxicity pathway perturbations applicable to ecological risk assessment. Domoic acid, an algal toxin with adverse effects on both wildlife and humans, is a potent agonist for kainate receptors (ionotropic glutamate receptors whose activation leads to the influx of Na+ and Ca2+). Increased Ca2+ concentrations result in neuronal excitotoxicity and cell death, primarily in the hippocampus, which produces seizures, impairs learning and memory, and alters behavior in some species. Altered neuronal Ca2+ is a key process in domoic acid toxicity, which can be evaluated in vitro. Furthermore, results of these assays would be amenable to mechanistic modeling for identifying domoic acid concentrations and Ca2+ perturbations that are normal, adaptive, or clearly toxic. In vitro assays with outputs amenable to measurement in exposed populations can link in vitro to in vivo conditions, and toxicokinetic information will aid in linking in vitro results to the individual organism. Development of an AOP required an iterative process with three important outcomes: a critically reviewed, stressor-specific AOP; identification of key processes suitable for evaluation with in vitro assays; and strategies for model development.

Original languageEnglish (US)
Pages (from-to)9-21
Number of pages13
JournalEnvironmental Toxicology and Chemistry
Volume30
Issue number1
DOIs
StatePublished - Jan 2011
Externally publishedYes

Fingerprint

Toxicity
Assays
acid
toxicity
modeling
perturbation
Ionotropic Glutamate Receptors
Kainic Acid Receptors
Population dynamics
ecotoxicology
Poisons
Ecotoxicology
Cell death
Risk assessment
toxin
Population Dynamics
population dynamics
risk assessment
learning
Chemical activation

Keywords

  • Algal
  • Calcium
  • Hippocampus
  • Neurobehavioral
  • Toxin

ASJC Scopus subject areas

  • Health, Toxicology and Mutagenesis
  • Environmental Chemistry

Cite this

Defining and modeling known adverse outcome pathways : Domoic acid and neuronal signaling as a case study. / Watanabe-Sailor, Karen; Andersen, Melvin E.; Basu, Niladri; Carvan, Michael J.; Crofton, Kevin M.; King, Kerensa A.; Suñol, Cristina; Tiffany-Castiglioni, Evelyn; Schultz, Irvin R.

In: Environmental Toxicology and Chemistry, Vol. 30, No. 1, 01.2011, p. 9-21.

Research output: Contribution to journalArticle

Watanabe-Sailor, K, Andersen, ME, Basu, N, Carvan, MJ, Crofton, KM, King, KA, Suñol, C, Tiffany-Castiglioni, E & Schultz, IR 2011, 'Defining and modeling known adverse outcome pathways: Domoic acid and neuronal signaling as a case study', Environmental Toxicology and Chemistry, vol. 30, no. 1, pp. 9-21. https://doi.org/10.1002/etc.373
Watanabe-Sailor, Karen ; Andersen, Melvin E. ; Basu, Niladri ; Carvan, Michael J. ; Crofton, Kevin M. ; King, Kerensa A. ; Suñol, Cristina ; Tiffany-Castiglioni, Evelyn ; Schultz, Irvin R. / Defining and modeling known adverse outcome pathways : Domoic acid and neuronal signaling as a case study. In: Environmental Toxicology and Chemistry. 2011 ; Vol. 30, No. 1. pp. 9-21.
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