Skip to main content
Journal cover image

Expanding the test set: Chemicals with potential to disrupt mammalian brain development.

Publication ,  Journal Article
Mundy, WR; Padilla, S; Breier, JM; Crofton, KM; Gilbert, ME; Herr, DW; Jensen, KF; Radio, NM; Raffaele, KC; Schumacher, K; Shafer, TJ; Cowden, J
Published in: Neurotoxicology and teratology
November 2015

High-throughput test methods including molecular, cellular, and alternative species-based assays that examine critical events of normal brain development are being developed for detection of developmental neurotoxicants. As new assays are developed, a "training set" of chemicals is used to evaluate the relevance of individual assays for specific endpoints. Different training sets are necessary for each assay that would comprise a developmental neurotoxicity test battery. In contrast, evaluation of the predictive ability of a comprehensive test battery requires a set of chemicals that have been shown to alter brain development after in vivo exposure ("test set"). Because only a small number of substances have been well documented to alter human neurodevelopment, we have proposed an expanded test set that includes chemicals demonstrated to adversely affect neurodevelopment in animals. To compile a list of potential developmental neurotoxicants, a literature review of compounds that have been examined for effects on the developing nervous system was conducted. The search was limited to mammalian studies published in the peer-reviewed literature and regulatory studies submitted to the U.S. EPA. The definition of developmental neurotoxicity encompassed changes in behavior, brain morphology, and neurochemistry after gestational or lactational exposure. Reports that indicated developmental neurotoxicity was observed only at doses that resulted in significant maternal toxicity or were lethal to the fetus or offspring were not considered. As a basic indication of reproducibility, we only included a chemical if data on its developmental neurotoxicity were available from more than one laboratory (defined as studies originating from laboratories with a different senior investigator). Evidence from human studies was included when available. Approximately 100 developmental neurotoxicity test set chemicals were identified, with 22% having evidence in humans.

Duke Scholars

Altmetric Attention Stats
Dimensions Citation Stats

Published In

Neurotoxicology and teratology

DOI

EISSN

1872-9738

ISSN

0892-0362

Publication Date

November 2015

Volume

52

Issue

Pt A

Start / End Page

25 / 35

Related Subject Headings

  • Toxicology
  • Toxicity Tests
  • Reproducibility of Results
  • Prenatal Exposure Delayed Effects
  • Pregnancy
  • Neurotoxins
  • Mammals
  • Humans
  • High-Throughput Screening Assays
  • Female
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Mundy, W. R., Padilla, S., Breier, J. M., Crofton, K. M., Gilbert, M. E., Herr, D. W., … Cowden, J. (2015). Expanding the test set: Chemicals with potential to disrupt mammalian brain development. Neurotoxicology and Teratology, 52(Pt A), 25–35. https://doi.org/10.1016/j.ntt.2015.10.001
Mundy, William R., Stephanie Padilla, Joseph M. Breier, Kevin M. Crofton, Mary E. Gilbert, David W. Herr, Karl F. Jensen, et al. “Expanding the test set: Chemicals with potential to disrupt mammalian brain development.Neurotoxicology and Teratology 52, no. Pt A (November 2015): 25–35. https://doi.org/10.1016/j.ntt.2015.10.001.
Mundy WR, Padilla S, Breier JM, Crofton KM, Gilbert ME, Herr DW, et al. Expanding the test set: Chemicals with potential to disrupt mammalian brain development. Neurotoxicology and teratology. 2015 Nov;52(Pt A):25–35.
Mundy, William R., et al. “Expanding the test set: Chemicals with potential to disrupt mammalian brain development.Neurotoxicology and Teratology, vol. 52, no. Pt A, Nov. 2015, pp. 25–35. Epmc, doi:10.1016/j.ntt.2015.10.001.
Mundy WR, Padilla S, Breier JM, Crofton KM, Gilbert ME, Herr DW, Jensen KF, Radio NM, Raffaele KC, Schumacher K, Shafer TJ, Cowden J. Expanding the test set: Chemicals with potential to disrupt mammalian brain development. Neurotoxicology and teratology. 2015 Nov;52(Pt A):25–35.
Journal cover image

Published In

Neurotoxicology and teratology

DOI

EISSN

1872-9738

ISSN

0892-0362

Publication Date

November 2015

Volume

52

Issue

Pt A

Start / End Page

25 / 35

Related Subject Headings

  • Toxicology
  • Toxicity Tests
  • Reproducibility of Results
  • Prenatal Exposure Delayed Effects
  • Pregnancy
  • Neurotoxins
  • Mammals
  • Humans
  • High-Throughput Screening Assays
  • Female