Evidence map›Paper›PMID 30632520›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

Fangchinoline Promotes Autophagy and Inhibits Apoptosis in Osteoporotic Rats.

Wenjun Zhu, Wenge Ding, Xiaojun Shang, Ding Zhu, Xiaoyu Dai

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 32% 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, 13 citations in OpenAlex.

  1. Article
  2. Retracted: Fangchinoline Promotes Autophagy and Inhibits Apoptosis in Osteoporotic Rats.Medical science monitor : international medical journal of experimental and clinical research · 2022
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  4. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Wenjun ZhuDepartment of Trauma Orthopedics, First People's Hospital of Changzhou Affiliated to Soochow University, Changzhou, Jiangsu, China (mainland).
Wenge DingDepartment of Trauma Orthopedics, First People's Hospital of Changzhou Affiliated to Soochow University, Changzhou, Jiangsu, China (mainland).
Xiaojun ShangDepartment of Trauma Orthopedics, First People's Hospital of Changzhou Affiliated to Soochow University, Changzhou, Jiangsu, China (mainland).
Ding ZhuDepartment of Trauma Orthopedics, First People's Hospital of Changzhou Affiliated to Soochow University, Changzhou, Jiangsu, China (mainland).
Xiaoyu DaiDepartment of Trauma Orthopedics, First People's Hospital of Changzhou Affiliated to Soochow University, Changzhou, Jiangsu, China (mainland).
The First People's Hospital of Changzhou · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Osteoporosis is a common disorder leading to bone loss. At present, the treatment options available for the management of osteoporosis are limited. The present investigation evaluated the protective effect of fangchinoline against osteoporosis and also postulates the possible mechanism of action. MATERIAL AND METHODS Osteoporosis was induced by subcutaneously injecting prednisolone (2.5 mg/pellet) for 4 weeks. Fangchinoline 1, 3 and 10 mg/kg was given intraperitoneally for the period. Protective effects of fangchinoline were assessed by estimating microarchitectural parameters and bone mineral density (BMD) in the vertebrae tissues, and biochemical parameters were also determined in the serum of rats with prednisolone-induced osteoporosis. Moreover, gene expression of microtubule-associated protein 1A/1B-light chain 3 (LC3), B cell lymphoma 2 (Bcl-2), caspase-3, bone morphogenetic protein 2 (BMP2), Beclin-1, autophagy-related 5 (ATG-5), Runt-related transcription factor 2 (RUNX-2), and receptor activator of nuclear factor kappa-b ligand (RANKL) protein in the vertebrae tissue were assessed by reverse transcription-polymerase chain reaction (RT-PCR) and Western blot assay. RESULTS There was a significant (p<0.01) decrease in the BMD and microarchitectural parameters in the vertebrae tissue of the fangchinoline-treated group compared to the prednisolone group. We also found that treatment with fangchinoline attenuated the altered expressions of LC3, Bcl-2, caspase-3, BMP2, Beclin-1, ATG-5, RUNX-2, and RANKL protein in the prednisolone-induced osteoporosis rats. Moreover, levels of biochemical parameters were attenuated in the serum of fangchinoline-treated and prednisolone-induced osteoporosis rat. Histopathology revealed that the apoptosis of osteoblasts was decreased in the fangchinoline-treated group compared to the prednisolone group of rats. CONCLUSIONS Fangchinoline inhibits apoptosis of osteoblasts and protects against bone loss in prednisolone-induced osteoporosis rats by inducing autophagy.

Indexed as

AnimalsApoptosisAutophagyBenzylisoquinolinesBone DensityBone ResorptionChinaDisease Models, AnimalMaleOsteoblastsOsteoporosisPrednisoloneRatsRats, WistarBenzylisoquinolinesfangchinolinePrednisolone

Identifiers

PMID30632520
PMCPMC6338015
OpenAlexW2910789077

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.