Evidence map›Paper›PMID 25815520›Full record

ArticleMolecular medicine reports2015

Effects of OsteoKing on osteoporotic rabbits.

Lifen Dai, Haiying Wu, Shan Yu, Hongbin Zhao, Lanjie Xue, Ming Xu, Zhiqiang Shen, Min Hu

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Osteoking improves OP rat by enhancing HSP90‑β expression.International journal of molecular medicine · 2020
    Article
  5. Rabbit as model for osteoporosis research.Journal of bone and mineral metabolism · 2019
    Review
  6. Article
  7. Article
  8. 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

8 authors at 4 institutions in 1 country.

Lifen DaiSchool of Pharmaceutical Science and Yunnan Key Laboratory of Pharmacology for Natural Products, Kunming Medical University, Kunming, Yunnan 650500, P.R. China.
Haiying WuTrauma Center of Emergency Medicine Department, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650032, P.R. China.
Shan YuResearch Center for Molecular Medicine, Kunming University, Kunming, Yunnan 650214, P.R. China.
Hongbin ZhaoTrauma Center of Emergency Medicine Department, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan 650032, P.R. China.
Lanjie XueFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan 650500, P.R. China.
Ming XuResearch Center for Molecular Medicine, Kunming University, Kunming, Yunnan 650214, P.R. China.
Zhiqiang ShenSchool of Pharmaceutical Science and Yunnan Key Laboratory of Pharmacology for Natural Products, Kunming Medical University, Kunming, Yunnan 650500, P.R. China.
Min HuResearch Center for Molecular Medicine, Kunming University, Kunming, Yunnan 650214, P.R. China.
Kunming Medical University · CNKunming University · CNFirst Affiliated Hospital of Kunming Medical University · CNKunming University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heng-Gu-Gu-Shang-Yu-He-Ji, also known as OsteoKing, is used as a herbal Traditional Chinese Medicine for the treatment of bone disease, including femoral head necrosis and osteoarthritis. However, whether OsteoKing has anti-osteoporotic properties has remained to be elucidated. The purpose of the present study was therefore to investigate the effects of OsteoKing on ovariectomy-induced osteoporosis in rabbits. Female New Zealand white rabbits were randomly divided into an ovariectomized (OVX) group and a sham-surgery group. The rabbits in the OVX group were subjected to an ovariectomy, while the rabbits in the sham group were subjected to the removal of an area of fat near the two ovaries. Bone mineral density, mechanical properties, serum biochemical parameters and micro-architecture were examined at 150 days post-OVX to characterize the experimental animal model. Once the osteoporotic rabbit model had been established, the rabbits in the OVX group were divided into the following groups: Model group, nilestriol group and 300 and 600 mg/kg OsteoKing groups, containing 16 rabbits in each group. OsteoKing and nilestriol were administered orally. The bone mineral density, mechanical properties, serum biochemical parameters, histology and micro-architecture were examined using dual-energy X-ray absorptiometric analysis, mechanical assessments, enzyme-linked immunosorbent assays, histopathological evaluation and micro-computerized tomography examination following 60 days and 120 days of treatment, respectively. Treatment with OsteoKing led to an elevation in the bone mineral density of the vertebra and serum phosphorus levels, reduced serum concentrations of osteocalcin, procollagen type I N-terminal peptide, tartrate-resistant acid phosphatase 5b and cross-linked N-telopeptide of type I collagen, improved mechanical properties (maximum load, stiffness and energy absorption capacity), and micro-architecture of the lumbar vertebra in the OVX osteoporotic rabbit model following treatment for 120 days. In conclusion, it was demonstrated that OsteoKing is effective in the prevention of estrogen deficiency-associated bone loss and may be a promising drug for the treatment of post-menopausal osteoporosis.

Indexed as

Absorptiometry, PhotonAcid PhosphataseAdministration, OralAnimalsBone DensityBone Density Conservation AgentsDrugs, Chinese HerbalEstriolEstrogensFemaleIsoenzymesLumbar VertebraeOsteocalcinOsteoporosisOvariectomyPeptide FragmentsAcid PhosphataseBone Density Conservation AgentsDrugs, Chinese HerbalEstriolEstrogensIsoenzymesnylestriolOsteocalcinosteokingPeptide FragmentsPhosphorusProcollagenprocollagen Type I N-terminal peptideQuinestrolTartrate-Resistant Acid Phosphatase

Identifiers

PMID25815520
PMCPMC4438876
OpenAlexW2030861926

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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.