Evidence map›Paper›PMID 37849329›Full record

ReviewDisaster medicine and public health preparedness2023

Skin Models Used to Define Mechanisms of Action of Sulfur Mustard.

Jeffrey D Laskin, Kevin Ozkuyumcu, Peihong Zhou, Claire R Croutch, Diane E Heck, Debra L Laskin, Laurie B Joseph

Open access · hybridAbstract readReview
In one paragraph

Review in Disaster medicine and public health preparedness, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.0field-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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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 3 institutions in 1 country.

Jeffrey D LaskinDepartment of Environmental and Occupational Health and Justice, Rutgers University School of Public Health, Piscataway, NJ, USA.
Kevin OzkuyumcuDepartment of Pharmacology and Toxicology, Ernest Mario School of Pharmacy, Piscataway, NJ, USA.
Peihong ZhouDepartment of Pharmacology and Toxicology, Ernest Mario School of Pharmacy, Piscataway, NJ, USA.
Claire R CroutchMRIGlobal, Kansas City, MO, USA.
Diane E HeckDepartment of Pharmacology and Toxicology, Ernest Mario School of Pharmacy, Piscataway, NJ, USA.
Debra L LaskinDepartment of Pharmacology and Toxicology, Ernest Mario School of Pharmacy, Piscataway, NJ, USA.ORCID 0000-0003-1832-7311
Laurie B JosephDepartment of Pharmacology and Toxicology, Ernest Mario School of Pharmacy, Piscataway, NJ, USA.
Environmental and Occupational Health Sciences Institute · USMRIGlobal · USRutgers, The State University of New Jersey · US

Funding

UMDNJ/Rutgers University CounterACT Research Center of ExcellenceU54AR055073 · NIAMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI LASKIN, DEBRA L · 2006 to 2024
$71.4M
Translational Research Support CoreP30ES005022 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI BRIAN T BUCKLEY · 1988 to 2026
$47.4M
TRAINING IN EVIRONMENTAL TOXICOLOGYT32ES007148 · NIEHS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI Lauren M Aleksunes · 1987 to 2026
$11.4M
ACTIVATED MACROPHAGES AND OZONE TOXICITYR01ES004738 · NIEHS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI Debra L Laskin · 1989 to 2026
$9.0M
Harnessing Inflammatory Macrophages to Thwart Lung Disease Caused by Chronic Ozone ExposureR01ES033698 · NIEHS · RUTGERS, THE STATE UNIV OF N.J. · PI Debra L Laskin · 2022 to 2026
$2.8M
NIAMS NIH HHS U54 AR055073NIEHS NIH HHS P30 ES005022NIEHS NIH HHS R01 ES004738NIEHS NIH HHS R01 ES033698NIEHS NIH HHS T32 ES007148
6 · The paper itself

Abstract

Sulfur mustard (SM) is a threat to both civilian and military populations. Human skin is highly sensitive to SM, causing delayed erythema, edema, and inflammatory cell infiltration, followed by the appearance of large fluid-filled blisters. Skin wound repair is prolonged following blistering, which can result in impaired barrier function. Key to understanding the action of SM in the skin is the development of animal models that have a pathophysiology comparable to humans such that quantitative assessments of therapeutic drugs efficacy can be assessed. Two animal models, hairless guinea pigs and swine, are preferred to evaluate dermal products because their skin is morphologically similar to human skin. In these animal models, SM induces degradation of epidermal and dermal tissues but does not induce overt blistering, only microblistering. Mechanisms of wound healing are distinct in these animal models. Whereas a guinea pig heals by contraction, swine skin, like humans, heals by re-epithelialization. Mice, rats, and rabbits are also used for SM mechanistic studies. However, healing is also mediated by contraction; moreover, only microblistering is observed. Improvements in animal models are essential for the development of therapeutics to mitigate toxicity resulting from dermal exposure to SM.

Indexed as

Mustard GasAnimalsGuinea PigsHumansMiceRabbitsRatsSkinMustard Gasanimal modelsdermatotoxicitysulfur mustardwound healing

Identifiers

PMID37849329
PMCPMC11420828
OpenAlexW4387729077

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.