Evidence map›Paper›PMID 40007249›Full record

ArticleJournal of periodontal research2025

Xanthine Derivative KMUP-3 Alleviates Periodontal Bone Resorption by Inhibiting Osteoclastogenesis and Macrophage Pyroptosis.

Shang-En Huang, Kai-Fang Hu, Meng-Xuan Lin, Ching-Jiunn Tseng, Bin-Nan Wu, Zen-Kong Dai, Jong-Hau Hsu, Jwu-Lai Yeh

Abstract read
In one paragraph

Article in Journal of periodontal research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Shang-En HuangDepartment of Pharmacology, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.ORCID https://orcid.org/0000-0003-2324-9178
Kai-Fang HuInstitute of Clinical Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Meng-Xuan LinDepartment of Pharmacology, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Ching-Jiunn TsengInstitute of Clinical Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Bin-Nan WuDepartment of Pharmacology, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Zen-Kong DaiDepartment of Pediatrics, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Jong-Hau HsuDepartment of Pediatrics, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.ORCID https://orcid.org/0000-0002-2690-7247
Jwu-Lai YehDepartment of Pharmacology, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.ORCID https://orcid.org/0000-0001-7101-5865

Funding

Kaohsiung Medical University KMU-DK(A)113001National Science and Technology Council NSTC112-2320-B-037-019-MY3,112-2811-B-037-008,and111-2314-B-037-075-MY3
6 · The paper itself

Abstract

aimThis study investigated the function effects of KMUP-3, a self-developed synthetic xanthine-based derivative, in suppressing Porphyromonas gingivalis (Pg-LPS)-aggravated osteoclastogenesis and pyroptosis as a potential treatment for periodontitis.

methodsIn vitro, the effects of Pg-LPS and KMUP-3 on osteoclast formation and macrophage pyroptosis were investigated using the receptor activator of nuclear factor-κB ligand (RANKL)-primed RAW264.7 macrophages. In vivo, the therapeutic effects of KMUP-3 were evaluated in a model of experimental periodontitis induced by gingival ligature placement.

resultsWe reveal that KMUP-3 suppressed osteoclastogenesis, inducible nitric oxide synthase activation, and reduced nitric oxide production enhanced by Pg-LPS in RANKL-primed RAW264.7 cells while also decreasing TLR4/NF-κB p65 pathway activation and decreased pro-inflammatory cytokine production; moreover, Pg-LPS promoted NLRP3 activation and exacerbated pyroptosis induction effects that were abolished by KMUP-3. Finally, KMUP-3 ameliorated alveolar bone loss and IL-1β levels in the gingival crevicular fluid in the rat ligature periodontitis model.

conclusionsOur study demonstrated that KMUP-3 attenuates Pg-LPS-enhanced osteoclastogenesis and macrophage pyroptosis. Notably, KMUP-3 alleviates alveolar bone loss in experimental periodontitis rats and thus suggests its certain role in safeguarding against periodontal bone resorption.

Indexed as

Alveolar Bone LossMacrophagesOsteoclastsOsteogenesisPeriodontitisPyroptosisAnimalsDisease Models, AnimalInterleukin-1betaLipopolysaccharidesMaleMiceNitric OxideNLR Family, Pyrin Domain-Containing 3 ProteinPorphyromonas gingivalisRANK LigandInterleukin-1betaLipopolysaccharidesNitric OxideNLR Family, Pyrin Domain-Containing 3 ProteinRANK Ligandalveolar bone lossnitric oxideosteoclastogenesispyroptosisxanthine derivative KMUP‐3

Identifiers

PMID40007249
PMCPMC12371823

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.