Evidence map›Paper›PMID 39679857›Full record

ArticleImmunity, inflammation and disease2024

Zoledronic Acid Inhibits Lipopolysaccharide-Induced Osteoclastogenesis by Suppressing Macrophage NLRP3-Mediated Autophagy Pathway.

Yuting Cheng, Guanjuan Liu, Xiaolin Huang, Yue Xiong, Na Song, Zheqing An, Wei Hong, Chidchanok Leethanakul, Bancha Samruajbenjakun, Jian Liao

Abstract read
In one paragraph

Article in Immunity, inflammation and disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Autophagy: regulating the seesaw of bone-fat balance.Frontiers in cell and developmental biology · 2025
    Review
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

10 authors.

Yuting ChengSchool/Hospital of Stomatology, Guizhou Medical University, Guiyang, China.
Guanjuan LiuSchool/Hospital of Stomatology, Guizhou Medical University, Guiyang, China.
Xiaolin HuangHospital of Stomatology, Zhongshan City, Zhongshan, China.
Yue XiongSchool/Hospital of Stomatology, Guizhou Medical University, Guiyang, China.
Na SongSchool/Hospital of Stomatology, Guizhou Medical University, Guiyang, China.
Zheqing AnSchool/Hospital of Stomatology, Guizhou Medical University, Guiyang, China.
Wei HongKey Laboratory of Endemic and Ethnic Diseases, Guizhou Medical University, Ministry of Education, Guiyang, China.
Chidchanok LeethanakulFaculty of Dentistry, Prince of Songkla University, Hat Yai, Thailand.
Bancha SamruajbenjakunFaculty of Dentistry, Prince of Songkla University, Hat Yai, Thailand.ORCID 0000-0001-8429-9828
Jian LiaoSchool/Hospital of Stomatology, Guizhou Medical University, Guiyang, China.

Funding

The present study was supported by the Natural Science Foundation of China (grant nos. 82260198 and 82060207), the Science and Technology Foundation of Guizhou Provincial Health Commission (grant no. gzwkj2023-437) and the Foundation of School/Hospital of Stomatology of Guizhou Medical University (grant no. GYKQKY2022-03).
6 · The paper itself

Abstract

introductionInflammatory factors leading to bone loss significantly increase the risk of tooth loosening or implantation failure. Zoledronic acid (ZOL) is a widely used medication for effectively inhibiting excessive bone destruction, but its effect on alleviating inflammatory bone loss remains to be elucidated. In this study, we investigated whether ZOL alleviates inflammatory bone resorption through immunomodulatory effect.

methodsThe viability of the cells was evaluated by Cell Counting Kit 8 (CCK8) assay. Osteoclast (OC) differentiation and function were determined by tartrate-resistant acid phosphatase (TRAP) staining and bone resorption pits assays, respectively. Autophagosomes and actin ring structures of OC were observed using transmission electron microscopy (TEM) and F-actin ring staining, respectively. The microstructure in mice maxillary alveolar bone model was observed by micro computed tomography (Miro-CT). Reverse transcription-quantitative PCR (RT-qPCR) to detect the mRNA expression of osteoclast-related genes and Western blot (WB) analysis to evaluate the protein expression levels of autophagy-related proteins and the NOD-like receptor family pyrin domain-containing protein 3 (NLRP3)-related proteins in pre-OCs.

resultsThe findings indicated that ZOL hindered lipopolysaccharide (LPS)-mediated OC differentiation, formation, bone resorption activity and autophagosome levels. Furthermore, ZOL diminished the expression of genes associated with OC. And the expression of proteins ATG7, LC3II, Beclin1, NLRP3-related proteins and tumor necrosis factor-α (TNF-α) protein were markedly decreased while P62 was increased, especially in the 1 μM ZOL group or MCC950 + ZOL group.

conclusionsZOL has a certain immunomodulatory effect that exhibits anti-inflammatory properties at lower concentrations, which can weaken LPS-induced OCs differentiation and function, and NLRP3-mediated autophagy pathway may participate in this process.

Indexed as

AutophagyLipopolysaccharidesMacrophagesNLR Family, Pyrin Domain-Containing 3 ProteinOsteoclastsOsteogenesisZoledronic AcidAnimalsBone ResorptionCell DifferentiationMiceMice, Inbred C57BLRAW 264.7 CellsSignal TransductionLipopolysaccharidesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseZoledronic Acidautophagybone resorptionlipopolysaccharideNLRP3osteoclastzoledronic acid

Identifiers

PMID39679857
PMCPMC11647992

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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.