Evidence map›Paper›PMID 31595219›Full record

ArticleCogent biology2019

The Cardiopulmonary Effects of Sodium Fluoroacetate (1080) in Sprague-Dawley Rats.

Bryan J McCranor, Talearia D Young, Justin Tressler, Laura Jennings, James Irwin, Nazira A Alli, Marilynda K Abilez, Samuel Stone, Michelle Racine, Jennifer L Devorak and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Cogent biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

Bryan J McCranorUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
Talearia D YoungUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
Justin TresslerUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
Laura JenningsUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
James IrwinUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
Nazira A AlliUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
Marilynda K AbilezUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
Samuel StoneUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
Michelle RacineUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
Jennifer L DevorakUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
Alfred M SciutoUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
Benjamin WongUS Army Medical Research Institute of Chemical Defense, 8350 Ricketts Point Rd, APG, MD 21010.
DEVCOM Army Research Laboratory · US

Funding

XFe96 AnalyzerS10OD018015 · OD · VANDERBILT UNIVERSITY · PI LANNIGAN, DEBORAH · 2014 to 2014
$200k
NIH HHS AOD18015-001
6 · The paper itself

Abstract

Sodium fluoroacetate (1080) is a highly toxic metabolic poison that has the potential because of its lack of defined color, odor, and taste and its high water solubility to be intentionally or unintentionally ingested through food adulteration. Although the mechanism of action for 1080 has been known since the 1950's, no known antidote exists. In an effort to better understand the cardiopulmonary impacts of 1080, we utilized whole-body plethysmography and telemeterized Sprague-Dawley rats which allowed for the real-time measurement of respiratory and cardiac parameters following exposure using a non-invasive assisted-drinking method. Overall, the animals showed marked depression of respiratory parameters over the course of 24 hours post-exposure and the development of hemorrhage in the lung tissue. Tidal volume was reduced by 30% in males and 60% in females at 24 hours post-exposure, and respiratory frequency was significantly depressed as well. In telemeterized female rats, we observed severe cardiac abnormalities, highlighted by a 50% reduction in heart rate, 75% reduction in systolic blood pressure, and a 3.5-fold lengthening of the QRS interval over the course of 24 hours. We also observed a reduction in core body temperature of nearly 15°C. Our study was able to describe the severe and pronounced effects of sodium fluoroacetate poisoning on cardiopulmonary function, the results of which indicate that both tissue specific and systemic deficits contribute to the toxicological progression of 1080 intoxication and will need to be accounted for when developing any potential countermeasure for 1080 poisoning.

Indexed as

1080cardiopulmonarymetabolic poisonPesticidesReal-Time PhysiologySodium fluoroacetateToxicology

Identifiers

PMID31595219
PMCPMC6782068
OpenAlexW2911172372

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.