Evidence map›Paper›PMID 30046042›Full record

ArticleScientific reports2018

Isosteviol Derivative Inhibits Osteoclast Differentiation and Ameliorates Ovariectomy-Induced Osteoporosis.

Huey-En Tzeng, Po-Hao Huang, Chun-Hao Tsai, Gregory J Tsay, Yi-Ju Lee, Tsurng-Juhn Huang, Tzu-Hung Lin, Ying-Ming Chiu, Yi-Ying Wu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
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  5. 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

9 authors at 5 institutions in 1 country.

Huey-En TzengTaipei Cancer Center, Taipei Medical University, Taipei, Taiwan.
Po-Hao HuangDepartment of Internal Medicine, School of Medicine, China Medical University Hospital and China Medical University, Taichung, Taiwan.
Chun-Hao TsaiDepartment of Orthopedics, School of Medicine, China Medical University Hospital and China Medical University, Taichung, Taiwan.ORCID 0000-0002-4428-3132
Gregory J TsayDepartment of Internal Medicine, School of Medicine, China Medical University Hospital and China Medical University, Taichung, Taiwan.
Yi-Ju LeeInstitute of Biochemistry, Microbiology and Immunology, Chung Shan Medical University, Taichung, Taiwan.
Tsurng-Juhn HuangDepartment of Biochemistry, China Medical University, Taichung, Taiwan.
Tzu-Hung LinMaterial and Chemical Research Laboratories, Industrial Technology Research Institute, Chutung, Hsinchu County, Taiwan.
Ying-Ming ChiuDivision of Allergy, Immunology & Rheumatology, Changhua Christian Hospital, Changhua, Taiwan.
Yi-Ying WuDepartment of Medical Laboratory Science and Biotechnology, China Medical University, Taichung, Taiwan. yyw@mail.cmu.edu.tw.
China Medical University · TWChanghua Christian Hospital · TWChung Shan Medical University · TWIndustrial Technology Research Institute · TWTaipei Medical University-Shuang Ho Hospital · TW

Funding

Changhua Christian Hospital (CCH) 106-CCH-IRP-055
6 · The paper itself

Abstract

NC-8 (ent-16-oxobeyeran-19-N-methylureido) is an isosteviol-derived analogue with multiple biological effects, including anti-inflammation and anti-bacterial activities and inhibition of HBV viral surface antigen gene expression. In this study, we explored the effects of NC-8 on the formation of osteoclasts from RAW 264.7 cells. We found that NC-8 exerts the novel effect of inhibiting osteoclast-like cell formation. Our experiments showed that RANKL-induced ERK, p38, and JNK phosphorylation were inhibited by NC-8. An ovariectomy-induced osteoporosis animal model was used to examine the protective effects of oral treatment with NC-8. Serum analysis was used to examine markers of osteoblasts, osteoclasts, and renal and hepatic function in rats. Micro CT scanning and histological analysis were used to measure bone loss in ovariectomized rats. Oral administration of NC-8 effectively decreased excess bone resorption and significantly antagonized trabecular bone loss in ovariectomized rats. Serum analysis of C-terminal telopeptide of type-I collagen, an osteoclast marker, also showed that NC-8 administration inhibited excess bone resorption. Furthermore, serum analysis showed that renal and liver function were not affected by these doses of NC-8 during long-term treatment. Our results demonstrate that NC-8 inhibits osteoclast differentiation and effectively ameliorates ovariectomy-induced osteoporosis.

Indexed as

AnimalsBone ResorptionCell DifferentiationDiterpenes, KauraneHumansLiverMAP Kinase Kinase 4MAP Kinase Signaling SystemMiceOsteoblastsOsteoclastsOsteoporosisOvariectomyp38 Mitogen-Activated Protein KinasesPhosphorylationRatsDiterpenes, KauraneisosteviolMAP Kinase Kinase 4p38 Mitogen-Activated Protein Kinases

Identifiers

PMID30046042
PMCPMC6060097
OpenAlexW2883670451

What OpenQuestion holds

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LicenceCC BY
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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.