Evidence map›Paper›PMID 35056817›Full record

ArticleMolecules (Basel, Switzerland)2022

Melatonin Attenuates RANKL-Induced Osteoclastogenesis via Inhibition of Atp6v0d2 and DC-STAMP through MAPK and NFATc1 Signaling Pathways.

Seong-Sik Kim, Soon-Pill Jeong, Bong-Soo Park, In-Ryoung Kim

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  3. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
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  15. Frontiers in cellular and infection microbiology · 2022
    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

4 authors at 2 institutions in 1 country.

Seong-Sik KimDepartment of Orthodontics, Dental Research Institute, Pusan National University Dental Hospital, Yangsan 50612, Korea.
Soon-Pill JeongDepartment of Orthodontics, Dental Research Institute, Pusan National University Dental Hospital, Yangsan 50612, Korea.
Bong-Soo ParkDepartment of Oral Anatomy, School of Dentistry, Pusan National University, Yangsan 50612, Korea.
In-Ryoung KimDepartment of Oral Anatomy, School of Dentistry, Pusan National University, Yangsan 50612, Korea.ORCID 0000-0003-0232-0385
Pusan National University · KRPusan National University Dental Hospital · KR

Funding

National Research Foundation of Korea NRF-2019R1A2C108405712
6 · The paper itself

Abstract

Melatonin is a hormone secreted by the pineal gland that is involved in the biorhythm of reproductive activities. The present study investigated the inhibitory effects of melatonin on osteoclastogenesis in RAW 264.7 cells according to changes in V-ATPase and the corresponding inhibition of the MAPK and NFATc1 signaling processes.

methodsthe cytotoxic effect of melatonin was investigated by MTT assay. Osteoclast differentiation and gene expression of osteoclast-related factors were confirmed via TRAP staining, pit formation assay, immunofluorescence imaging, western blot, and real-time PCR.

resultsmelatonin was found to inactivate the p38 and JNK of MAP kinase in RAW264.7 cells treated with RANKL and treated with a combination RANKL and melatonin for 1, 3, and 5 days. The melatonin treatment group showed a reduction in osteoclastogenesis transcription factors and ATP6v0d2 gene expression.

conclusionsmelatonin inhibits osteoclast differentiation and cell fusion by inhibiting the expression of Atp6v0d2 through the inactivation of MAPK and NFATc1 signaling in RANKL-stimulated RAW264.7 macrophages. The findings of the present study suggest that melatonin could be a suitable therapy for bone loss and imply a potential role of melatonin in bone health.

Indexed as

OsteogenesisAnimalsAntioxidantsBone ResorptionCell DifferentiationCells, CulturedDown-RegulationGene Expression RegulationMacrophagesMelatoninMembrane ProteinsMiceMitogen-Activated Protein KinasesNerve Tissue ProteinsNFATC Transcription FactorsNF-kappa BAntioxidantsAtp6v0d2 protein, mouseDC-STAMP protein, mouseMelatoninMembrane ProteinsMitogen-Activated Protein KinasesNerve Tissue ProteinsNfatc1 protein, mouseNFATC Transcription FactorsNF-kappa BVacuolar Proton-Translocating ATPasesbone remodelingmelatoninosteoclastogenesisosteoporosisV-ATPase

Identifiers

PMID35056817
PMCPMC8781594
OpenAlexW4205614098

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.