Evidence map›Paper›PMID 27441211›Full record

ArticleHeliyon2015

Donepezil prevents RANK-induced bone loss via inhibition of osteoclast differentiation by downregulating acetylcholinesterase.

Tsuyoshi Sato, Yuichiro Enoki, Yasushi Sakamoto, Kazuhiro Yokota, Masahiko Okubo, Masahito Matsumoto, Naoki Hayashi, Michihiko Usui, Shoichiro Kokabu, Toshihide Mimura and 7 more

Abstract read
In one paragraph

Article in Heliyon, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Effects of Donepezil on the Musculoskeletal System in Female Rats.International journal of molecular sciences · 2023
    Article
  8. Review
  9. Article
  10. Review
  11. Brain-Derived Acetylcholine Maintains Peak Bone Mass in Adult Female Mice.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2020
    Article
  12. Acetylcholinesterase Inhibitors Are Associated with Reduced Fracture Risk among Older Veterans with Dementia.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2020
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. 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

17 authors.

Tsuyoshi SatoDepartment of Oral and Maxillofacial Surgery, Saitama Medical University, Saitama, Japan.
Yuichiro EnokiDepartment of Oral and Maxillofacial Surgery, Saitama Medical University, Saitama, Japan.
Yasushi SakamotoDepartment of Biomedical Research Center, Division of Analytical Science, Saitama Medical University, Saitama, Japan.
Kazuhiro YokotaDepartment of Rheumatology and Applied Immunology, Saitama Medical University, Saitama, Japan.
Masahiko OkuboDepartment of Oral and Maxillofacial Surgery, Saitama Medical University, Saitama, Japan; Division of Functional Genomics and Systems Medicine, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan.
Masahito MatsumotoDivision of Functional Genomics and Systems Medicine, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan.
Naoki HayashiDepartment of Oral and Maxillofacial Surgery, Saitama Medical University, Saitama, Japan.
Michihiko UsuiDepartment of Periodontology, Kyushu Dental University, Fukuoka, Japan.
Shoichiro KokabuDivision of Molecular Signaling and Biochemistry, Department of Health Promotion, Kyushu Dental University, Fukuoka, Japan.
Toshihide MimuraDepartment of Rheumatology and Applied Immunology, Saitama Medical University, Saitama, Japan.
Yoshihiko NakazatoDepartment of Neurology, Saitama Medical University, Saitama, Japan.
Nobuo ArakiDepartment of Neurology, Saitama Medical University, Saitama, Japan.
Toru FukudaDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University, Tokyo, Japan.
Yasushi OkazakiDivision of Functional Genomics and Systems Medicine, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan.
Tatsuo SudaDivision of Functional Genomics and Systems Medicine, Research Center for Genomic Medicine, Saitama Medical University, Saitama, Japan.
Shu TakedaDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University, Tokyo, Japan.
Tetsuya YodaDepartment of Oral and Maxillofacial Surgery, Saitama Medical University, Saitama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDonepezil, an inhibitor of acetylcholinesterase (AChE) targeting the brain, is a common medication for Alzheimer's disease. Interestingly, a recent clinical study found that administration of this agent is associated with lower risk of hip fracture independently of falling, suggesting its direct effect on bone tissues as well. AChE has been reported to be involved in osteoblast function, but the role of AChE on osteoclastogenesis still remains unclear. We analyzed the effect of AChE and donepezil on osteoclastogenesis in vivo and in vitro.

methodsCell-based assays were conducted using osteoclasts generated in cultures of murine bone marrow macrophages (BMMs) with receptor activator of nuclear factor-kappa B ligand (RANKL). The effect of donepezil was also determined in vivo using a mouse model of RANKL-induced bone loss.

resultsRecombinant AChE in BMMs cultured with RANKL further promoted RANKL-induced tartrate-resistant acid phosphatase (TRAP)-positive osteoclast differentiation. RANKL also upregulated AChE expression in BMMs. RNA interference-mediated knockdown of AChE significantly inhibited RANKL-induced osteoclast differentiation and suppressed gene expression specific for osteoclasts. AChE upregulated expression of RANK, the receptor of RANKL, in BMMs. Donepezil decreased cathepsin K expression in BMMs and the resorptive function of osteoclasts on dentine slices. Donepezil decreased RANK expression in BMMs, resulting in the inhibition of osteoclast differentiation with downregulation of c-Fos and upregulation of Id2. Moreover, administration of donepezil prevented RANKL-induced bone loss in vivo, which was associated with the inhibition of bone resorption by osteoclasts.

conclusionsAChE promotes osteoclast differentiation in vitro. Donepezil inhibits osteoclast function in vitro and prevents bone loss by suppressing bone resorption in vivo, suggesting the possibility that donepezil reduces fracture risk in patients with Alzheimer's disease.

Indexed as

AcetylcholinesteraseAlzheimer's diseaseDifferentiationDonepezilOsteoclast

Identifiers

PMID27441211
PMCPMC4939821

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.