Evidence map›Paper›PMID 28481322›Full record

ArticleInternational journal of molecular sciences2017

Imipramine Protects against Bone Loss by Inhibition of Osteoblast-Derived Microvesicles.

Lili Deng, Ying Peng, Yuhai Jiang, Yu Wu, Yuedi Ding, Yaping Wang, Dong Xu, Qiang Fu

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Article
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  3. Review
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  5. Isolation of Extracellular Vesicle Subtypes from Primary Osteoblast Cultures.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Exosomes: A Tool for Bone Tissue Engineering.Tissue engineering. Part B, Reviews · 2022
    Review
  11. Exosome mediated biological functions within skeletal microenvironment.Frontiers in bioengineering and biotechnology · 2022
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
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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.

Lili DengKey Laboratory of Nuclear Medicine, Ministry of Health, Jiangsu Institute of Nuclear Medicine, Wuxi 214063, Jiangsu, China. denglili@jsinm.org.
Ying PengKey Laboratory of Nuclear Medicine, Ministry of Health, Jiangsu Institute of Nuclear Medicine, Wuxi 214063, Jiangsu, China. pengying@jsinm.org.
Yuhai JiangWuxi Second People's Hospital of Nanjing Medical University, Wuxi 214123, Jiangsu, China. jyh_wj@sina.com.
Yu WuWuxi Medical School, Jiangnan University, Wux i214122, Jiangsu, China. wuyu@jiangnan.edu.cn.
Yuedi DingKey Laboratory of Nuclear Medicine, Ministry of Health, Jiangsu Institute of Nuclear Medicine, Wuxi 214063, Jiangsu, China. dingyuedi@jsinm.org.
Yaping WangWuxi Second People's Hospital of Nanjing Medical University, Wuxi 214123, Jiangsu, China. ypwnag0301@126.com.
Dong XuKey Laboratory of Nuclear Medicine, Ministry of Health, Jiangsu Institute of Nuclear Medicine, Wuxi 214063, Jiangsu, China. xudong@jsinm.org.
Qiang FuKey Laboratory of Nuclear Medicine, Ministry of Health, Jiangsu Institute of Nuclear Medicine, Wuxi 214063, Jiangsu, China. qiangqfu@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The maintenance of bone homeostasis is largely dependent upon cellular communication between osteoclasts and osteoblasts. Microvesicles (MVs) represent a novel mechanism for osteoblasts and osteoclasts communication, as has been demonstrated in our previous study. Sphingomyelinases catalyze the hydrolysis of sphingomyelin, which leads to increased membrane fluidity and facilitates MV generation. This effect can be inhibited by imipramine, an inhibitor of acid sphingomyelinase (ASM), which is also known as a member of tricyclic antidepressants (TCAs). A recent study has reported that in vitro treatment of imipramine blocked MVs release from glial cells. However, whether imipramine has this effect on osteoblast-derived MVs and whether it is involved in MV generation in vivo is unclear. Here, our investigations found that imipramine slightly reduced the expression of osteoblast differentiation of related genes, but did not impact parathyroid hormone (PTH) regulation for these genes and also did not affect receptor activator of nuclear factor-κB ligand (RANKL)-mediated osteoclast formation; however, imipramine treatment blocked MVs released from osteoblasts and inhibited MV-induced osteoclast formation. In vivo, mice administrated with imipramine were protected from ovariectomy-induced bone loss as evaluated by various bone structural parameters and serum levels of biochemical markers. Our results suggest that inhibiting the production of MVs containing RANKL in vivo is very important for preventing bone loss.

Indexed as

AnimalsBone Density Conservation AgentsCell-Derived MicroparticlesCell DifferentiationCell LineCells, CulturedFemaleHumansImipramineMiceMice, Inbred C57BLNF-kappa BOsteoblastsOsteoclastsOsteoporosis, PostmenopausalParathyroid HormoneBone Density Conservation AgentsImipramineNF-kappa BParathyroid HormoneRANK Ligandbone losscellular communicationimipraminemicrovesicles

Identifiers

PMID28481322
PMCPMC5454926

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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.