Evidence map›Paper›PMID 39285937›Full record

ArticleCurrent research in toxicology2024

Investigation of inflammatory mechanisms induced by croton oil in mouse ear.

Ganming Mao, Dalon Douglas, Milankumar Prajapati, Trishaal Janardhanam Raghavendra Rao, Haiyan Zheng, Caifeng Zhao, Blase Billack

Abstract read
In one paragraph

Article in Current research in toxicology, 2024. 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Unlocking the therapeutic potential ofSouth African journal of botany : official journal of the South African Association of Botanists = Suid-Afrikaanse tydskrif vir plantkunde : amptelike tydskrif van die Suid-Afrikaanse Genootskap van Plantkundiges · 2026
    Article
  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.

Ganming MaoDepartment of Pharmaceutical Sciences, St. John's University, Queens, NY 11439, USA.
Dalon DouglasDepartment of Pharmaceutical Sciences, St. John's University, Queens, NY 11439, USA.
Milankumar PrajapatiDepartment of Pathology and Laboratory Medicine, Brown University, Providence, RI 02912, USA.
Trishaal Janardhanam Raghavendra RaoDepartment of Pharmaceutical Sciences, St. John's University, Queens, NY 11439, USA.
Haiyan ZhengCenter for Advanced Biotechnology and Medicine, Piscataway, NJ 08854, USA.
Caifeng ZhaoCenter for Advanced Biotechnology and Medicine, Piscataway, NJ 08854, USA.
Blase BillackDepartment of Pharmaceutical Sciences, St. John's University, Queens, NY 11439, USA.

Funding

Dermal-Epidermal Junction Disruptors: Toxicodynamic MechanismsR16GM149512 · NIGMS · ST. JOHN'S UNIVERSITY · PI Blase Christopher Billack · 2023 to 2026
$710k
Dermal-Epidermal Junction Disruptors: Mechanistic InsightsSC2GM136612 · NIGMS · ST. JOHN'S UNIVERSITY · PI BILLACK, BLASE CHRISTOPHER · 2020 to 2022
$369k
NIGMS NIH HHS R16 GM149512NIGMS NIH HHS SC2 GM136612
6 · The paper itself

Abstract

Croton oil is liquid at room temperature, with a pale-yellow color and spicy odor. It is commonly used in combination with phenol as a chemical peeling agent in dermatology, which reveals its caustic exfoliating effects. Topical use of croton oil at a high dose produces skin irritation, inflammation, swelling, pain, and even tumors. Therefore, croton oil has been widely used for inflammation, pain, and tumor related research, with different animal models having been established. However, mechanistic studies through which croton oil induces skin swelling, injury and activates tissue repair/regeneration are limited. The present study used croton oil to induce mouse ear edema and examined tissue responses 4 h after exposure. To this end, croton oil was applied to the ventral side of mouse ears, followed by tissue collection. Samples were analyzed by hematoxylin and eosin (H&E) staining, toluidine blue staining, and immunohistochemistry staining for myeloperoxidase (MPO) and matrix metalloproteinase-9 (MMP-9). Western blotting and ELISA were also carried out for MMP-9 together with unbiased proteomic analysis using mass-spectrometry. Results from our study demonstrated that as soon as 4 h of exposure to 2.5 % croton oil, the expression levels of MPO and MMP-9 in the dermis significantly increased compared to acetone-treated (vehicle) control ears, as did other inflammatory reactions such as swelling and neutrophil aggregation and infiltration. Subsequently, proteomic analysis confirmed that croton oil treatment resulted in significant upregulation of proteins such as myeloperoxidase (MPO), matrix metalloproteinase-9 (MMP-9), and matrix metalloproteinase-8 (MMP-8) in the ear skin. Interestingly, mouse ears treated with acetone vehicle showed differential expression of 2,478 proteins relative to naïve tissues; among those differentially expressed in acetone-treated samples were members of the phosphatidylinositol-glycan biosynthesis class N, T and U proteins (PIGN, PIGT, and PIGU). Overall, this work confirms the presence of neutrophil-derived MPO and MMP-9 and extends the body of knowledge to show that MMP-8 is also present during croton oil-mediated skin inflammation in the mouse ear; moreover, we find that acetone vehicle is not inert and has effects on the skin that should be considered moving forward.

Indexed as

Croton oilDermatotoxicityInflammationMMP-8MMP-9MyeloperoxidasePIGNPIGTPIGUSkin

Identifiers

PMID39285937
PMCPMC11403446

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.