Evidence map›Paper›PMID 16079074›Full record

ArticleEnvironmental health perspectives2005

Alterations in central nervous system serotonergic and dopaminergic synaptic activity in adulthood after prenatal or neonatal chlorpyrifos exposure.

Justin E Aldridge, Armando Meyer, Frederic J Seidler, Theodore A Slotkin

Open access · diamondAbstract read
In one paragraph

Article in Environmental health perspectives, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 3 pooled it
15.7field-weighted citation impact, top 1% 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

91 citing papers in PubMed, 3 syntheses or guidelines pooled it, 177 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pesticide exposure and neurodevelopmental outcomes: review of the epidemiologic and animal studies.Journal of toxicology and environmental health. Part B, Critical reviews · 2013
    Pooled it
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  13. Concentration-dependent effects of chlorpyrifos oxon on peroxisome proliferator-activated receptor signaling in MCF-7 cells.Toxicology in vitro : an international journal published in association with BIBRA · 2022
    Article
  14. Use of computational toxicology tools to predictCurrent research in toxicology · 2022
    Article
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31 more citing papers are in PubMed but not listed here.

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 1 institution in 2 countries.

Justin E AldridgeDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Armando Meyer
Frederic J Seidler
Theodore A Slotkin
Duke Medical Center · US

Funding

Zebrafish as a Detector of Organophosphate ExposureP42ES010356 · NIEHS · DUKE UNIVERSITY · PI EDWARD D LEVIN · 2000 to 2026
$56.2M
Integrated Toxicology ProgramT32ES007031 · NIEHS · DUKE UNIVERSITY · PI DI GIULIO, RICHARD · 1985 to 2007
$2.4M
MECHANISMS OF CHLORPYRIFOS DEVELOPMENTAL NEUROTOXICITYR01ES010387 · NIEHS · DUKE UNIVERSITY · PI SLOTKIN, THEODORE A · 2000 to 2004
$963k
NIEHS NIH HHS ES07031NIEHS NIH HHS ES10356NIEHS NIH HHS ES10387NIEHS NIH HHS P42 ES010356NIEHS NIH HHS R01 ES010387NIEHS NIH HHS T32 ES007031
6 · The paper itself

Abstract

Exposure to chlorpyrifos (CPF) alters neuronal development of serotonin (5HT) and dopamine systems, and we recently found long-term alterations in behaviors related to 5HT function. To characterize the synaptic mechanisms underlying these effects, we exposed developing rats to CPF regimens below the threshold for systemic toxicity, in three treatment windows: gestational days (GD) 17-20, postnatal days (PN) 1-4, or PN11-14. In early adulthood (PN60), we assessed basal neurotransmitter content and synaptic activity (turnover) in brain regions containing the major 5HT and dopamine projections. CPF exposure on GD17-20 or PN1-4 evoked long-term increases in 5HT turnover across multiple regions; the effects were not secondary to changes in neurotransmitter content, which was unaffected or even decreased. When the treatment window was shifted to PN11-14, there were no long-term effects. Dopamine turnover also showed significant increases after CPF exposure on GD17-20, but only when the dose was raised above the threshold for overt toxicity; however, hippocampal dopamine content was profoundly subnormal after exposures below or above the acute, toxic threshold, suggesting outright neurotoxicity. These results indicate that, in a critical developmental period, apparently nontoxic exposures to CPF produce lasting activation of 5HT systems in association with 5HT-associated behavioral anomalies.

Indexed as

3,4-Dihydroxyphenylacetic AcidAnimalsAnimals, NewbornBrainChlorpyrifosDopamineFemaleHomovanillic AcidInsecticidesMalePregnancyPrenatal Exposure Delayed EffectsRatsRats, Sprague-DawleySerotoninSynaptic Transmission3,4-Dihydroxyphenylacetic AcidChlorpyrifosDopamineHomovanillic AcidInsecticidesSerotonin

Identifiers

PMID16079074
PMCPMC1280344
OpenAlexW1995303792

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.