Evidence map›Paper›PMID 27904671›Full record

ArticleAmerican journal of translational research2016

Melatonin promotes diabetic wound healing in vitro by regulating keratinocyte activity.

Ruipeng Song, Lijun Ren, Haoli Ma, Ruijing Hu, Honghong Gao, Li Wang, Xuehui Chen, Zhigang Zhao, Jialin Liu

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Involvement of the SIRT1-NLRP3 pathway in the inflammatory response.Cell communication and signaling : CCS · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Protective Effects of Melatonin on the Skin: Future Perspectives.International journal of molecular sciences · 2019
    Review
  15. Article
  16. Review
  17. 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

9 authors at 1 institution in 1 country.

Ruipeng SongDepartment of Endocrinology, The Third People's Provincial Hospital of Henan Province Zhengzhou 450000, Henan, China.
Lijun RenDepartment of Endocrinology, The Third People's Provincial Hospital of Henan Province Zhengzhou 450000, Henan, China.
Haoli MaDepartment of Endocrinology, The Third People's Provincial Hospital of Henan Province Zhengzhou 450000, Henan, China.
Ruijing HuDepartment of Endocrinology, The Third People's Provincial Hospital of Henan Province Zhengzhou 450000, Henan, China.
Honghong GaoDepartment of Endocrinology, The Third People's Provincial Hospital of Henan Province Zhengzhou 450000, Henan, China.
Li WangDepartment of Endocrinology, The Third People's Provincial Hospital of Henan Province Zhengzhou 450000, Henan, China.
Xuehui ChenDepartment of Endocrinology, The Third People's Provincial Hospital of Henan Province Zhengzhou 450000, Henan, China.
Zhigang ZhaoDepartment of Endocrinology, Henan Provincial People's Hospital Zhengzhou 450000, Henan, China.
Jialin LiuSchool of Life Science and Technology, Shanghai Tech University Shanghai 201210, China.
ShanghaiTech University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic patients are at high risk of developing delayed cutaneous wound healing. Proper keratinocyte proliferation and migration are crucial steps during re-epithelialization. Melatonin (Mel) accelerates wound repair in full-thickness incisional wounds; however, its role in diabetic wound healing is unknown. This study explored the role of Mel in diabetic wound healing in vitro by using high glucose (HG)-cultured keratinocytes. Mel reduced the HG-induced mRNA expression and release of pro-inflammatory cytokines, including tumor necrosis factor-α, interleukin (IL)-1β, IL-6, and IL-8, in keratinocytes. Mel inhibited oxidative stress, as evidenced by reduced production of reactive oxygen species and malondialdehyde and increased activity of superoxide dismutase in HG-stimulated keratinocytes. Mel also inhibited HG-induced nucleotide binding oligomerization domain-like receptor family pyrin domain-containing 3 inflammasome activation in keratinocytes. HG-induced reduced migration and proliferation and increased apoptosis of keratinocytes were counteracted by Mel treatment. The pro-proliferative, pro-migratory, and anti-apoptotic effects of Mel on HG-treated keratinocytes were mediated by extracellular signal-regulated kinase signaling pathway. Results collectively suggested that Mel is an alternative therapeutic strategy to ameliorate poor condition for diabetic wound healing by regulating keratinocyte activity.

Indexed as

chronic inflammationDiabetic wound healinghigh glucosekeratinocytemelatoninoxidative stress

Identifiers

PMID27904671
PMCPMC5126313
OpenAlexW2559811960

What OpenQuestion holds

Textmetadata
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.