Evidence map›Paper›PMID 14998743›Full record

ArticleEnvironmental health perspectives2004

Critical periods for chlorpyrifos-induced developmental neurotoxicity: alterations in adenylyl cyclase signaling in adult rat brain regions after gestational or neonatal exposure.

Armando Meyer, Frederic J Seidler, Justin E Aldridge, Charlotte A Tate, Mandy M Cousins, Theodore A Slotkin

Open access · diamondAbstract read
In one paragraph

Article in Environmental health perspectives, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
7.5field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
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  7. Review
  8. Article
  9. Induction of endocannabinoid levels in juvenile rat brain following developmental chlorpyrifos exposure.Toxicological sciences : an official journal of the Society of Toxicology · 2013
    Article
  10. Effect of developmental chlorpyrifos exposure, on endocannabinoid metabolizing enzymes, in the brain of juvenile rats.Toxicological sciences : an official journal of the Society of Toxicology · 2011
    Article
  11. Review
  12. 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

6 authors at 1 institution in 1 country.

Armando MeyerCentro de Estudos da Saúde do Trabalhador e Ecologia Humana, Escola Nacional de Saúde Pública, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Frederic J Seidler
Justin E Aldridge
Charlotte A Tate
Mandy M Cousins
Theodore A Slotkin
Escola Nacional de Saúde Pública · BR

Funding

Zebrafish as a Detector of Organophosphate ExposureP42ES010356 · NIEHS · DUKE UNIVERSITY · PI EDWARD D LEVIN · 2000 to 2026
$56.2M
MECHANISMS OF CHLORPYRIFOS DEVELOPMENTAL NEUROTOXICITYR01ES010387 · NIEHS · DUKE UNIVERSITY · PI SLOTKIN, THEODORE A · 2000 to 2004
$963k
NIEHS NIH HHS ES 10356NIEHS NIH HHS ES 10387
6 · The paper itself

Abstract

Developmental exposure to chlorpyrifos (CPF) alters the function of a wide variety of neural systems. In the present study we evaluated the effects in adulthood of CPF exposure of rats during different developmental windows, using the adenylyl cyclase (AC) signaling cascade, which mediates the cellular responses to numerous neurotransmitters. Animals were exposed on gestational days (GD) 9-12 or 17-20 or on postnatal days (PN) 1-4 or 11-14 and assessed at PN60. In addition to basal AC activity, we evaluated the responses to direct AC stimulants (forskolin, Mn2+) and to isoproterenol, which activates signaling through ss-adrenoceptors coupled to stimulatory G-proteins. CPF exposure in any of the four periods elicited significant changes in AC signaling in a wide variety of brain regions in adulthood. In general, GD9-12 was the least sensitive stage, requiring doses above the threshold for impaired maternal weight gain, whereas effects were obtained at subtoxic doses for all other regimens. Most of the effects were heterologous, involving signaling elements downstream from the receptors, and thus shared by multiple stimulants; superimposed on this basic pattern, there were also selective alterations in receptor-mediated responses, in G-protein function, and in AC expression and subtypes. Exposures conducted at GD17-20 and later all produced sex-selective alterations. These results suggest that developmental exposure to CPF elicits long-lasting alterations in cell-signaling cascades that are shared by multiple neurotransmitter and hormonal inputs; the resultant abnormalities of synaptic communication are thus likely to occur in widespread neural circuits and their corresponding behaviors.

Indexed as

Prenatal Exposure Delayed EffectsAdenylyl CyclasesAdrenergic beta-AgonistsAnimalsBrainChlorpyrifosDose-Response Relationship, DrugFemaleInsecticidesIsoproterenolMalePregnancyRatsRats, Sprague-DawleyReceptors, Adrenergic, betaSignal TransductionAdenylyl CyclasesAdrenergic beta-AgonistsChlorpyrifosInsecticidesIsoproterenolReceptors, Adrenergic, beta

Identifiers

PMID14998743
PMCPMC1241857
OpenAlexW2062754962

What OpenQuestion holds

Textmetadata
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.