Evidence map›Paper›PMID 29355495›Full record

ArticleHormones and behavior2018

Endocrine active metals, prenatal stress and enhanced neurobehavioral disruption.

Marissa Sobolewski, Katherine Conrad, Elena Marvin, Joshua L Allen, Deborah A Cory-Slechta

Open access · greenAbstract read
In one paragraph

Article in Hormones and behavior, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Endocrine disruptors, aryl hydrocarbon receptor and cortisol secretion.Journal of endocrinological investigation · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Prenatal metal mixtures and sex-specific infant negative affectivity.Environmental epidemiology (Philadelphia, Pa.) · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Marissa SobolewskiDept. of Environmental Medicine, University of Rochester School of Medicine, Rochester, NY, United States. Electronic address: marissa:sobolewski@urmc.rochester.edu.
Katherine ConradDept. of Environmental Medicine, University of Rochester School of Medicine, Rochester, NY, United States.
Elena MarvinDept. of Environmental Medicine, University of Rochester School of Medicine, Rochester, NY, United States.
Joshua L AllenDept. of Environmental Medicine, University of Rochester School of Medicine, Rochester, NY, United States.
Deborah A Cory-SlechtaDept. of Environmental Medicine, University of Rochester School of Medicine, Rochester, NY, United States.
University of Rochester · USUniversity of Rochester Medical Center · US

Funding

VISUAL INDICES OF NEUROTOXICITYP30ES001247 · NIEHS · UNIVERSITY OF ROCHESTER · PI Sally W Thurston · 1985 to 2026
$42.8M
CNS Glucocorticoid Epigenetic Changes of Pb Stress EffectsR01ES021534 · NIEHS · UNIVERSITY OF ROCHESTER · PI CORY-SLECHTA, DEBORAH A, SCHNEIDER, JAY S · 2013 to 2017
$2.3M
NIEHS NIH HHS L40 ES028596NIEHS NIH HHS P30 ES001247NIEHS NIH HHS R01 ES021534
6 · The paper itself

Abstract

Metals, including lead (Pb), methylmercury (MeHg) and arsenic (As), are long-known developmental neurotoxicants. More recently, environmental context has been recognized to modulate metals toxicity, including nutritional state and stress exposure. Modulation of metal toxicity by stress exposure can occur through shared targeting of endocrine systems, such as the hypothalamic-pituitary-adrenal axis (HPA). Our previous rodent research has identified that prenatal stress (PS) modulates neurotoxicity of two endocrine active metals (EAMs), Pb and MeHg, by altering HPA and CNS systems disrupting behavior. Here, we review this research and further test the hypothesis that prenatal stress modulates metals neurotoxicity by expanding to test the effect of developmental As ± PS exposure. Serum corticosterone and behavior was assessed in offspring of dams exposed to As ± PS. PS increased female offspring serum corticosterone at birth, while developmental As exposure decreased adult serum corticosterone in both sexes. As + PS induced reductions in locomotor activity in females and reduced response rates on a Fixed Interval schedule of reinforcement in males, with the latter suggesting unique learning deficits only in the combined exposure. As-exposed males showed increased time in the open arms of an elevated plus maze and decreased novel object recognition whereas females did not. These data further confirm the hypothesis that combined exposure to chemical (EAMs) and non-chemical (PS) stressors results in enhanced neurobehavioral toxicity. Given that humans are exposed to multiple environmental risk factors that alter endocrine function in development, such models are critical for risk assessment and public health protection, particularly for children.

Indexed as

Prenatal Exposure Delayed EffectsStress, PsychologicalAnimalsAnimals, NewbornArsenicBehavior, AnimalCorticosteroneEndocrine DisruptorsFemaleHypothalamo-Hypophyseal SystemMaleMental DisordersMetalsMiceMice, Inbred C57BLPituitary-Adrenal SystemArsenicCorticosteroneEndocrine DisruptorsMetalsArsenicBehaviorCorticosteroneLeadMetalsMethylmercuryPrenatal stress

Identifiers

PMID29355495
PMCPMC5970043
OpenAlexW2789103057

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.