Evidence map›Paper›PMID 26097549›Full record

ArticleInternational journal of clinical and experimental pathology2015

Ursolic acid derivative ameliorates streptozotocin-induced diabestic bone deleterious effects in mice.

Su-Guo Yu, Cheng-Jie Zhang, Xiu-E Xu, Ji-Hua Sun, Li Zhang, Peng-Fei Yu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 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
0.8field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Food science & nutrition · 2024
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Ursolic Acid and Its Derivatives as Bioactive Agents.Molecules (Basel, Switzerland) · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. Ursolic acid in health and disease.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2018
    Review
  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

6 authors at 3 institutions in 1 country.

Su-Guo YuDepartment of Endocrinology, Affiliated Hosptial of Binzhou Medical University Binzhou 256603, China.
Cheng-Jie ZhangDepartment of Emergency, People's Hospital of Binzhou Binzhou 256610, China.
Xiu-E XuDepartment of Endocrinology, Hospital of Yangxin Traditional Chinese Medicine Binzhou 251880, China.
Ji-Hua SunDepartment of Endocrinology, Affiliated Hosptial of Binzhou Medical University Binzhou 256603, China.
Li ZhangDepartment of Endocrinology, Affiliated Hosptial of Binzhou Medical University Binzhou 256603, China.
Peng-Fei YuDepartment of Endocrinology, Affiliated Hosptial of Binzhou Medical University Binzhou 256603, China.
Binzhou Medical University · CNBinzhou People's Hospital · CNShanxi Province Hospital of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study was performed to investigate bone deteriorations of diabetic mice in response to the treatment of ursolic acid derivative (UAD).

methodsThe biomarkers in serum and urine were measured, tibias were taken for the measurement on gene and protein expression and histomorphology analysis, and femurs were taken for the measurement on bone Ca and three-dimensional architecture of trabecular bone.

resultsUAD showed a greater increase in bone Ca, BMD and significantly increased FGF-23 and OCN, reduced PTH and CTX in diabetic mice. UAD reversed STZ-induced trabecular deleterious effects and stimulated bone remodeling. The treatment of STZ group with UAD significantly elevated the ratio of OPG/RANKL. Moreover, insulin and IGF-1 showed a negative correlation with both FBG and Hb1Ac in STZ group. We attributed down-regulating the level of Hb1Ac in diabetic mice to that ursolic acid derivative could primely control blood sugar levels. After analyzing of two adipocyte markers, PPARγ and aP2, increased expression in the tibias of diabetic mice, and UAD could improve STZ-induced adipocyte dysfunction.

conclusionsThese results demonstrated that UAD could ameliorate STZ-induced bone deterioration through improving adipocyte dysfunction and enhancing new bone formation and inhibiting absorptive function of osteoclast in the bone of diabetic mice.

Indexed as

AnimalsBone DensityCalciumDiabetes Mellitus, ExperimentalFemurFibroblast Growth Factor-23InsulinInsulin-Like Growth Factor IMaleMiceMice, Inbred C57BLOsteoprotegerinRANK LigandTibiaTriterpenesUrsolic AcidCalciumFgf23 protein, mouseFibroblast Growth Factor-23InsulinInsulin-Like Growth Factor IOsteoprotegerinRANK LigandTriterpenesUrsolic AcidbonediabeticOPG/RANKLPPARγursolic acid derivative

Identifiers

PMID26097549
PMCPMC4466936
OpenAlexW2409390911

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.