Evidence map›Paper›PMID 20727709›Full record

ArticleReproductive toxicology (Elmsford, N.Y.)2010

Effects of prenatal exposure to a low dose atrazine metabolite mixture on pubertal timing and prostate development of male Long-Evans rats.

Jason P Stanko, Rolondo R Enoch, Jennifer L Rayner, Christine C Davis, Douglas C Wolf, David E Malarkey, Suzanne E Fenton

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Reproductive toxicology (Elmsford, N.Y.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. The effect of chronic inflammation on female fertility.Reproduction (Cambridge, England) · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Atrazine exposure in gestation and breastfeeding affects Calomys laucha sperm cells.Environmental science and pollution research international · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Embryonic Atrazine Exposure Elicits Alterations in Genes Associated with Neuroendocrine Function in Adult Male Zebrafish.Toxicological sciences : an official journal of the Society of Toxicology · 2016
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Endocrine disruptors and the breast: early life effects and later life disease.Journal of mammary gland biology and neoplasia · 2013
    Review
  18. Review
  19. Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 5 institutions in 1 country.

Jason P StankoReproductive Toxicology Division, US Environmental Protection Agency (US EPA), ORD/NHEERL, Research Triangle Park, NC 27711, USA.
Rolondo R Enoch
Jennifer L Rayner
Christine C Davis
Douglas C Wolf
David E Malarkey
Suzanne E Fenton
Environmental Protection Agency · USResearch Triangle Park Foundation · USNational Institute of Environmental Health Sciences · USNorth Carolina Central University · USUniversity of North Carolina at Chapel Hill · US

Funding

Mammary Gland as a Sensitive End Point to Effects of Endocrine DisruptorsZIAES102785 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI FENTON, SUZANNE · 2010 to 2021
$38.1M
Intramural NIH HHS Z99 ES999999
6 · The paper itself

Abstract

The present study examines the postnatal reproductive development of male rats following prenatal exposure to an atrazine metabolite mixture (AMM) consisting of the herbicide atrazine and its environmental metabolites diaminochlorotriazine, hydroxyatrazine, deethylatrazine, and deisopropylatrazine. Pregnant Long-Evans rats were treated by gavage with 0.09, 0.87, or 8.73mg AMM/kg body weight (BW), vehicle, or 100mg ATR/kg BW positive control, on gestation days 15-19. Preputial separation was significantly delayed in 0.87 mg and 8.73mg AMM-exposed males. AMM-exposed males demonstrated a significant treatment-related increase in incidence and severity of inflammation in the prostate on postnatal day (PND) 120. A dose-dependent increase in epididymal fat masses and prostate foci were grossly visible in AMM-exposed offspring. These results indicate that a short, late prenatal exposure to mixture of chlorotriazine metabolites can cause chronic prostatitis in male LE rats. The mode of action for these effects is presently unclear.

Indexed as

Prenatal Exposure Delayed EffectsAdipose Tissue, WhiteAdiposityAnimalsAtrazineDose-Response Relationship, DrugEpididymisFemaleForeskinGestational AgeHerbicidesMaleNo-Observed-Adverse-Effect LevelPesticide ResiduesPregnancyProstateAtrazineHerbicidesPesticide Residues

Identifiers

PMID20727709
PMCPMC2993819
OpenAlexW2058317533

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.