Evidence map›Paper›PMID 34638983›Full record

ArticleInternational journal of molecular sciences2021

Anti-Osteoporotic Effect of Morroniside on Osteoblast and Osteoclast Differentiation In Vitro and Ovariectomized Mice In Vivo.

Chang Gun Lee, Jeonghyun Kim, Seung Hee Yun, Seokjin Hwang, Hyoju Jeon, Eunkuk Park, Seon-Yong Jeong

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. 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
1.8field-weighted citation impact, top 14% 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, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Frontiers in medicine · 2023
    Review
  11. Article
  12. Article
  13. [Effects and mechanism of morroniside on osteogenic differentiation and proliferation of mouse MC3T3-E1 cells].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2022
    Article
  14. Review
  15. A Comparison of the Antiosteoporotic Effects of Cornelian Cherry (Oxidative medicine and cellular longevity · 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

7 authors at 1 institution in 1 country.

Chang Gun LeeDepartment of Medical Genetics, Ajou University School of Medicine, Suwon 16499, Korea.ORCID 0000-0002-2031-0802
Jeonghyun KimDepartment of Medical Genetics, Ajou University School of Medicine, Suwon 16499, Korea.
Seung Hee YunDepartment of Medical Genetics, Ajou University School of Medicine, Suwon 16499, Korea.
Seokjin HwangDepartment of Medical Genetics, Ajou University School of Medicine, Suwon 16499, Korea.
Hyoju JeonDepartment of Medical Genetics, Ajou University School of Medicine, Suwon 16499, Korea.
Eunkuk ParkDepartment of Medical Genetics, Ajou University School of Medicine, Suwon 16499, Korea.ORCID 0000-0002-1928-5531
Seon-Yong JeongDepartment of Medical Genetics, Ajou University School of Medicine, Suwon 16499, Korea.ORCID 0000-0002-0625-3530
Ajou University · KR

Funding

National Research Foundation of Korea (NRF) grant 2020R1I1A1A01072353National Research Foundation of Korea (NRF) grant 2021R1F1A1062311
6 · The paper itself

Abstract

Bone remodeling is a continuous process of bone synthesis and destruction that is regulated by osteoblasts and osteoclasts. Here, we investigated the anti-osteoporotic effects of morroniside in mouse preosteoblast MC3T3-E1 cells and mouse primary cultured osteoblasts and osteoclasts in vitro and ovariectomy (OVX)-induced mouse osteoporosis in vivo. Morroniside treatment enhanced alkaline phosphatase activity and positively stained cells via upregulation of osteoblastogenesis-associated genes in MC3T3-E1 cell lines and primary cultured osteoblasts. However, morroniside inhibited tartrate-resistant acid phosphatase activity and TRAP-stained multinucleated positive cells via downregulation of osteoclast-mediated genes in primary cultured monocytes. In the osteoporotic animal model, ovariectomized (OVX) mice were administered morroniside (2 or 10 mg/kg/day) for 12 weeks. Morroniside prevented OVX-induced bone mineral density (BMD) loss and reduced bone structural compartment loss in the micro-CT images. Taken together, morroniside promoted increased osteoblast differentiation and decreased osteoclast differentiation in cells, and consequently inhibited OVX-induced osteoporotic pathogenesis in mice. This study suggests that morroniside may be a potent therapeutic single compound for the prevention of osteoporosis.

Indexed as

AnimalsBone DensityBone Density Conservation AgentsBone RemodelingCell DifferentiationCell LineCell SurvivalCornusDisease Models, AnimalFemaleGlycosidesMiceMice, Inbred ICROsteoblastsOsteoclastsOsteogenesisBone Density Conservation AgentsGlycosidesmorronisidePlant Extractsbone remodelingmorronisideovariectomized miceprimary cultured osteoblastsprimary cultured osteoclasts

Identifiers

PMID34638983
PMCPMC8508973
OpenAlexW3203503086

What Socratic 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 Socratic graph.