Evidence map›Paper›PMID 28243795›Full record

ArticleJournal of bone and mineral metabolism2018

Minodronic acid induces morphological changes in osteoclasts at bone resorption sites and reaches a level required for antagonism of purinergic P2X2/3 receptors.

Makoto Tanaka, Akihiro Hosoya, Hiroshi Mori, Ryoji Kayasuga, Hiroaki Nakamura, Hidehiro Ozawa

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In one paragraph

Article in Journal of bone and mineral metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 2 institutions in 1 country.

Makoto TanakaResearch Promotion, Ono Pharmaceutical Co., Ltd., 3-1-1 Sakurai, Shimamoto, Osaka, 618-8585, Japan. mak.tanaka@ono.co.jp.
Akihiro HosoyaDepartment of Oral Histology, Matsumoto Dental University, Nagano, 399-0781, Japan.
Hiroshi MoriDiscovery Research Laboratories, Ono Pharmaceutical Co., Ltd., Shimamoto, Osaka, 618-8585, Japan.
Ryoji KayasugaDiscovery Research Laboratories, Ono Pharmaceutical Co., Ltd., Shimamoto, Osaka, 618-8585, Japan.
Hiroaki NakamuraDepartment of Oral Histology, Matsumoto Dental University, Nagano, 399-0781, Japan.
Hidehiro OzawaDepartment of Oral Histology, Matsumoto Dental University, Nagano, 399-0781, Japan.
Matsumoto Dental University · JPOno Pharmaceutical (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Minodronic acid is an aminobisphosphonate that is an antagonist of purinergic P2X2/3 receptors involved in pain. The aim of this study was to investigate the action and distribution of minodronic acid and the potential for P2X2/3 receptor antagonism based on the estimated concentration of minodronic acid. Microlocalization of radiolabeled minodronic acid was examined in the femur of neonatal rats. The bone-binding characteristics of minodronic acid and morphological changes in osteoclasts were analyzed in vitro. The minodronic acid concentration around bone resorption lacunae was predicted based on bone binding and the shape of lacunae. In microautoradiography, radioactive silver grains were abundant in bone-attached osteoclasts and were detected in calcified and ossification zones and in the cytoplasm of osteoclasts but not in the hypertrophic cartilage zone. In an osteoclast culture with 1 µM minodronic acid, 65% of minodronic acid was bound to bone, and C-terminal cross-linking telopeptide release was inhibited by 96%. Cultured osteoclasts without minodronic acid treatment formed ruffled borders and bone resorption lacunae and had rich cytoplasm, whereas those treated with 1 µM minodronic acid were not multinucleated, stained densely with toluidine blue, and were detached from the bone surface. In the 1 µM culture, the estimated minodronic acid concentration in resorption lacunae was 880 µM, which is higher than the IC

Indexed as

AnimalsAutoradiographyBone Density Conservation AgentsBone ResorptionCells, CulturedCortical BoneDiphosphonatesFemaleFemurImidazolesModels, BiologicalOsteoclastsPurinergic P2X Receptor AntagonistsRabbitsRatsReceptors, Purinergic P2X2Bone Density Conservation AgentsDiphosphonatesImidazolesPurinergic P2X Receptor AntagonistsReceptors, Purinergic P2X2Receptors, Purinergic P2X3YM 529BisphosphonateDistributionMinodronic acidOsteoclastP2X2/3 receptor

Identifiers

PMID28243795
OpenAlexW2594061097

What OpenQuestion holds

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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.