Evidence map›Paper›PMID 26439775›Full record

ArticleBirth defects research. Part B, Developmental and reproductive toxicology2015

Effect of Age, Duration of Exposure, and Dose of Atrazine on Sexual Maturation and the Luteinizing Hormone Surge in the Female Sprague-Dawley Rat.

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

Open access · hybridAbstract read
In one paragraph

Article in Birth defects research. Part B, Developmental and reproductive toxicology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Review
  3. Atrazine exposure in gestation and breastfeeding affects Calomys laucha sperm cells.Environmental science and pollution research international · 2019
    Article
  4. Article
  5. Article
  6. Low atrazine dosages reduce sperm quality of Calomys laucha mice.Environmental science and pollution research international · 2018
    Article
  7. PBPK Model for Atrazine and Its Chlorotriazine Metabolites in Rat and Human.Toxicological sciences : an official journal of the Society of Toxicology · 2016
    Article
  8. Review
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.

Charles B BreckenridgeDepartment of Toxicology and Health Sciences, Syngenta Crop Protection, LLC, Greensboro, North Carolina.
Pragati Sawhney CoderWIL Research, Ashland, Ohio.
Merrill O TisdelDepartment of Toxicology and Health Sciences, Syngenta Crop Protection, LLC, Greensboro, North Carolina.
James W SimpkinsDepartment of Physiology and Pharmacology, University of West Virginia, Morgantown, West Virginia.
Kun Don YiDepartment of Toxicology and Health Sciences, Syngenta Crop Protection, LLC, Greensboro, North Carolina.
Chad D ForadoriDepartment of Basic Medical Sciences, University of Arizona College of Medicine, Phoenix, Arizona.
Robert J HandaDepartment of Basic Medical Sciences, University of Arizona College of Medicine, Phoenix, Arizona.
Syngenta (United States) · USAshland (United States) · USColorado State University · USUniversity of Arizona · 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 (ATZ) was administered daily by gavage to pregnant female Sprague Dawley rats at doses of 0, 6.25, 25 or 50 mg/kg/day, either during gestation, lactation and post-weaning (G/L/PW cohort) to F1 generation female offspring or only from postnatal day (PND 21) until five days after sexual maturation (vaginal opening) when the estrogen-primed, luteinizing hormone (LH) surge was evaluated (PW cohort). Additional subgroups of F1 females received the vehicle or ATZ from PND 21-133 or from PND 120-133. Slight reductions in fertility and the percentage of F1 generation pups surviving to PND 21 in the gestationally exposed 50 mg/kg dose group were accompanied by decreased food intake and body weight of dams and F1 generation offspring. The onset of puberty was delayed in of the F1 generation G/L/PW females at doses of 25 and 50 mg/kg/day. F1 generation females in the PW high-dose ATZ group also experienced a delay in the onset of puberty. ATZ had no effect on peak LH or LH AUC in ovariectomized rats 5 days after sexual maturation, irrespective of whether the F1 generation females were treated from gestation onward or only peripubertally. There was no effect of ATZ treatment on the estrous cycle, peak LH or LH AUC of F1 generation females exposed from gestation through to PND 133 or only for two weeks from PND 120-133. These results indicate that developing females exposed to ATZ are not more sensitive compared to animals exposed to ATZ as young adults.

Indexed as

Environmental ExposureAgingAnimalsAtrazineBody WeightCrosses, GeneticEstradiolEstrous CycleFeeding BehaviorFemaleLuteinizing HormoneRatsRats, Sprague-DawleySexual MaturationSurvival AnalysisTime FactorsAtrazineEstradiolLuteinizing Hormonecyclicityhormonespostnatal evaluationrisk assessment

Identifiers

PMID26439775
PMCPMC4992940
OpenAlexW2174215431

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.