Evidence map›Paper›PMID 18977374›Full record

ArticleToxicology and applied pharmacology2009

Alterations in glucocorticoid negative feedback following maternal Pb, prenatal stress and the combination: a potential biological unifying mechanism for their corresponding disease profiles.

A Rossi-George, M B Virgolini, D Weston, D A Cory-Slechta

Open access · greenAbstract read
In one paragraph

Article in Toxicology and applied pharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 8% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Metal mixtures and adiposity indicators in women from Northern Mexico.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2025
    Article
  5. Article
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  7. Longitudinal association of early childhood lead exposure and adolescent heart rate variability: influence of parental education.Journal of environmental science and health. Part C, Toxicology and carcinogenesis · 2022
    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

4 authors at 3 institutions in 1 country.

A Rossi-GeorgeEnvironmental and Occupational Health Sciences Institute, a Joint Institute of the Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey and Rutgers, the State University of New Jersey, Piscataway, NJ 08854, USA.
M B Virgolini
D Weston
D A Cory-Slechta
University of Rochester · USEnvironmental and Occupational Health Sciences Institute · USRutgers, The State University of New Jersey · US

Funding

PB-Environmental Stress Interactions: Re-evaluating RiskR01ES012712 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI CORY-SLECHTA, DEBORAH A · 2005 to 2009
$2.4M
BEHAVIORAL TOXICITY OF LEAD--PHARMACOLOGICAL ANALYSISR01ES005017 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI CORY-SLECHTA, DEBORAH A · 1990 to 2004
$1.8M
NIEHS NIH HHS ES05017NIEHS NIH HHS R01 ES005017NIEHS NIH HHS R01 ES012712
6 · The paper itself

Abstract

Combined exposures to maternal lead (Pb) and prenatal stress (PS) can act synergistically to enhance behavioral and neurochemical toxicity in offspring. Maternal Pb itself causes permanent dysfunction of the body's major stress system, the hypothalamic pituitary adrenal (HPA) axis. The current study sought to determine the potential involvement of altered negative glucocorticoid feedback as a mechanistic basis of the effects in rats of maternal Pb (0, 50 or 150 ppm in drinking water beginning 2 mo prior to breeding), prenatal stress (PS; restraint on gestational days 16-17) and combined maternal Pb+PS in 8 mo old male and female offspring. Corticosterone changes were measured over 24 h following an i.p. injection stress containing vehicle or 100 or 300 microg/kg (females) or 100 or 150 microg/kg (males) dexamethasone (DEX). Both Pb and PS prolonged the time course of corticosterone reduction following vehicle injection stress. Pb effects were non-monotonic, with a greater impact at 50 vs. 150 ppm, particularly in males, where further enhancement occurred with PS. In accord with these findings, the efficacy of DEX in suppressing corticosterone was reduced by Pb and Pb+PS in both genders, with Pb efficacy enhanced by PS in females, over the first 6 h post-administration. A marked prolongation of DEX effects was found in males. Thus, Pb, PS and Pb+PS, sometimes additively, produced hypercortisolism in both genders, followed by hypocortisolism in males, consistent with HPA axis dysfunction. These findings may provide a plausible unifying biological mechanism for the reported links between Pb exposure and stress-associated diseases and disorders mediated via the HPA axis, including obesity, hypertension, diabetes, anxiety, schizophrenia and depression. They also suggest broadening of Pb screening programs to pregnant women in high stress environments.

Indexed as

Stress, PhysiologicalAnimalsAnimals, NewbornCorticosteroneDexamethasoneDose-Response Relationship, DrugFemaleHypothalamo-Hypophyseal SystemLeadMaleMaternal ExposureMaternal-Fetal ExchangePituitary-Adrenal SystemPregnancyPrenatal Exposure Delayed EffectsRatsCorticosteroneDexamethasoneLead

Identifiers

PMID18977374
PMCPMC2656375
OpenAlexW2160977326

What Socratic 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 Socratic graph.