Evidence map›Paper›PMID 24798751›Full record

ArticleInternational journal of molecular sciences2014

Topical N-acetylcysteine accelerates wound healing in vitro and in vivo via the PKC/Stat3 pathway.

Min-Ling Tsai, Hui-Pei Huang, Jeng-Dong Hsu, Yung-Rung Lai, Yu-Ping Hsiao, Fung-Jou Lu, Horng-Rong Chang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

33 citing papers in PubMed, 67 citations in OpenAlex.

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  11. Biological Activities ofMolecules (Basel, Switzerland) · 2023
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  19. International journal of molecular sciences · 2021
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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

7 authors at 2 institutions in 1 country.

Min-Ling TsaiInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan. cshd050@csh.org.tw.
Hui-Pei HuangInstitute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung 40201, Taiwan. hhpei@csmu.edu.tw.
Jeng-Dong HsuDepartment of Pathology, Chung Shan Medical University Hospital, Taichung 40201, Taiwan. dongdong@csmu.edu.tw.
Yung-Rung LaiDepartment of Pharmacy, Chung Shan Medical University Hospital, Taichung 40201, Taiwan. cshd050@csh.org.tw.
Yu-Ping HsiaoInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan. missyuping@gmail.com.
Fung-Jou LuInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan. fjlu@csmu.edu.tw.
Horng-Rong ChangInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan. chrcsmu@gmail.com.
Chung Shan Medical University Hospital · TWChung Shan Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N-Acetylcysteine (Nac) is an antioxidant administered in both oral and injectable forms. In this study, we used Nac topically to treat burn wounds in vitro and in vivo to investigate mechanisms of action. In vitro, we monitored glutathione levels, cell proliferation, migration, scratch-wound healing activities and the epithelialization-related proteins, matrixmetalloproteinase-1 (MMP-1) and proteins involved in regulating the expression of MMP-1 in CCD-966SK cells treated with Nac. Various Nac concentrations (0.1, 0.5, and 1.0 mM) increased glutathione levels, cell viability, scratch-wound healing activities and migration abilities of CCD-966SK cells in a dose-dependent manner. The MMP-1 expression of CCD-966SK cells treated with 1.0 mM Nac for 24 h was significantly increased. Levels of phosphatidylinositol 3-kinase (PI3K), protein kinase C (PKC), janus kinase 1 (Jak1), signal transducer and activator of transcription 3 (Stat3), c-Fos and Jun, but not extracellular signal-regulated protein kinases 1 and 2 (Erk1/2), were also significantly increased in a dose-dependent manner compared to the controls. In addition, Nac induced collagenous expression of MMP-1 via the PKC/Stat3 signaling pathway. In vivo, a burn wound healing rat model was applied to assess the stimulation activity and histopathological effects of Nac, with 3.0% Nac-treated wounds being found to show better characteristics on re-epithelialization. Our results demonstrated that Nac can potentially promote wound healing activity, and may be a promising drug to accelerate burn wound healing.

Indexed as

AcetylcysteineAdministration, TopicalAnimalsAntioxidantsBurnsCell LineCell ProliferationHumansMaleMitogen-Activated Protein Kinase 1Protein Kinase CRatsRats, WistarSignal TransductionSkinSTAT3 Transcription FactorAcetylcysteineAntioxidantsMitogen-Activated Protein Kinase 1Protein Kinase CSTAT3 Transcription Factor

Identifiers

PMID24798751
PMCPMC4057691
OpenAlexW2024074049

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.