Evidence map›Paper›PMID 24831581›Full record

ArticleBirth defects research. Part B, Developmental and reproductive toxicology2014

The effect of atrazine administered by gavage or in diet on the LH surge and reproductive performance in intact female Sprague-Dawley and Long Evans rats.

Chad D Foradori, Prägati Sawhney Coder, Merrill Tisdel, Kun Don Yi, James W Simpkins, Robert J Handa, Charles B Breckenridge

Open access · bronzeAbstract read
In one paragraph

Article in Birth defects research. Part B, Developmental and reproductive toxicology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
7.6field-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

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Herbicide-related health risks: key mechanisms and a guide to mitigation strategies.Journal of occupational medicine and toxicology (London, England) · 2025
    Review
  3. Article
  4. Article
  5. PBPK Model for Atrazine and Its Chlorotriazine Metabolites in Rat and Human.Toxicological sciences : an official journal of the Society of Toxicology · 2016
    Article
  6. PBPK-Based Probabilistic Risk Assessment for Total Chlorotriazines in Drinking Water.Toxicological sciences : an official journal of the Society of Toxicology · 2016
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Multigeneration reproduction and male developmental toxicity studies on atrazine in rats.Birth defects research. Part B, Developmental and reproductive toxicology · 2014
    Article
  12. Developmental toxicity studies with atrazine and its major metabolites in rats and rabbits.Birth defects research. Part B, Developmental and reproductive toxicology · 2014
    Article
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

7 authors at 5 institutions in 1 country.

Chad D ForadoriDepartment of Anatomy, Physiology and Pharmacology, College of Veterinary Medicine, Auburn University, Auburn, Alabama.
Prägati Sawhney Coder
Merrill Tisdel
Kun Don Yi
James W Simpkins
Robert J Handa
Charles B Breckenridge
Syngenta (United States) · USAuburn University · USBattelle · USUniversity of Phoenix · USWest Virginia University · US

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Sally Lynn Hodder · 2012 to 2026
$81.0M
NIGMS NIH HHS U54 GM104942
6 · The paper itself

Abstract

Atrazine (ATR) blunts the hormone-induced luteinizing hormone (LH) surge, when administered by gavage (50-100 mg/kg/day for 4 days), in ovariectomized rats. In this study, we determined if comparable doses delivered either by gavage (bolus dose) or distributed in diet would reduce the LH surge and subsequently affect fertility in the intact female rat. ATR was administered daily to intact female Sprague-Dawley (SD) or Long Evans (LE) rats by gavage (0, 0.75 1.5, 3, 6, 10, 12, 50, or 100 mg/kg/day) or diet (0, 30, 100, 160, 500, 660, or 1460 ppm) during one complete 4-day estrous cycle, starting on day of estrus. Estrous status, corpora lutea, ova, and LH plasma concentrations were evaluated. A second cohort of animals was mated on the fourth treatment day. Fertility metrics were assessed on gestational day 20. A higher portion of LE rats had asynchronous estrous cycles when compared to SD rats both during pretreatment and in response to ATR (≥50 mg/kg). In contrast, bolus doses of ATR (≥50 mg/kg) inhibited the peak and area under the curve for the preovulatory LH surge in SD but not LE animals. Likewise, only bolus-treated SD, not LE, rats displayed reduced mean number of corpora lutea and ova. There were no effects of ATR administered by gavage on mating, gravid number, or fetus number. Dietary administration had no effect on any reproductive parameter measured. These findings indicate that short duration, high-bolus doses of ATR can inhibit the LH surge and reduce the number of follicles ovulated; however, dietary administration has no effect on any endocrine or reproductive outcomes.

Indexed as

AnimalsAtrazineDietDose-Response Relationship, DrugEstrous CycleFemaleHerbicidesLuteinizing HormoneRatsRats, Long-EvansRats, Sprague-DawleyReproductionAtrazineHerbicidesLuteinizing Hormonemating/fertilitypesticidesrisk assessment

Identifiers

PMID24831581
PMCPMC4227606
OpenAlexW1579949889

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.