Evidence map›Paper›PMID 38496895›Full record

ArticleHeliyon2024

Metformin alleviates junctional epithelium senescence via the AMPK/SIRT1/autophagy pathway in periodontitis induced by hyperglycemia.

Xiaoyuan Ye, Yumin Wang, Yanying Tian, Ruonan Bi, Mingyue Li, Chunyan Yang, Li Zhang, Yuguang Gao

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Efficacy of metformin as an adjunct in periodontitis: A systematic analysis.Journal of Taibah University Medical Sciences · 2026
    Review
  5. Review
  6. Article
  7. Resveratrol Attenuates HMolecular neurobiology · 2025
    Article
  8. Review
  9. Article
  10. Review
  11. Review
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  14. 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

8 authors at 1 institution in 1 country.

Xiaoyuan YeDepartment of Pediatrics and Preventive Dentistry, Binzhou Medical University Hospital, Binzhou, 256699, Shandong, China.
Yumin WangInstitute of Stomatology, Binzhou Medical University, Yantai, 264003, Shandong, China.
Yanying TianDepartment of Pediatrics and Preventive Dentistry, Binzhou Medical University Hospital, Binzhou, 256699, Shandong, China.
Ruonan BiDepartment of Pediatrics and Preventive Dentistry, Binzhou Medical University Hospital, Binzhou, 256699, Shandong, China.
Mingyue LiDepartment of Pediatrics and Preventive Dentistry, Binzhou Medical University Hospital, Binzhou, 256699, Shandong, China.
Chunyan YangInstitute of Stomatology, Binzhou Medical University, Yantai, 264003, Shandong, China.
Li ZhangInstitute of Stomatology, Binzhou Medical University, Yantai, 264003, Shandong, China.
Yuguang GaoDepartment of Pediatrics and Preventive Dentistry, Binzhou Medical University Hospital, Binzhou, 256699, Shandong, China.
Binzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The junctional epithelium (JE) serves a crucial protective role in the periodontium. High glucose-related aging results in accelerated barrier dysfunction of the gingival epithelium, which may be associated with diabetic periodontitis. Metformin, an oral hypoglycemic therapeutic, has been proposed as a anti-aging agent. This study aimed to clarify the effect of metformin on diabetic periodontitis and explore its mechanism in ameliorating senescence of JE during hyperglycemia. The db/db mice was used as a diabetic model mice and alterations in the periodontium were observed by hematoxylin-eosin staining and immunohistochemistry. An ameloblast-like cell line (ALC) was cultured with high glucose to induce senescence. Cellular senescence and oxidative stress were evaluated by SA-β-gal staining and Intracellular reactive oxygen species (ROS) levels. Senescence biomarkers, P21 and P53, and autophagy markers, LC3-II/LC3-I, were measured by western blotting and quantitative real-time PCR. To construct a stable SIRT1 (Sirtuin 1) overexpression cell line, we transfected ALCs with lentiviral vectors overexpressing the mouse SIRT1 gene. Cellular senescence was increased in the JE of db/db mice and the periodontium was destroyed, which could be alleviated by metformin. Moreover, oxidative stress and cellular senescence in a high glucose environment were reduced by metformin in

Indexed as

HyperglycemiaJunctional epitheliumMetforminOxidative stressPeriodontitisSenescence

Identifiers

PMID38496895
PMCPMC10944230
OpenAlexW4392590175

What OpenQuestion 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 OpenQuestion graph.