Evidence map›Paper›PMID 34165588›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2021

FK506 ameliorates osteoporosis caused by osteoblast apoptosis via suppressing the activated CaN/NFAT pathway during oxidative stress.

Jian Jie, Weilin Li, Guihua Wang, Xiaoming Xu

Abstract read
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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Foods (Basel, Switzerland) · 2024
    Article
  4. Review
  5. Article
  6. The role of wnt signaling in diabetes-induced osteoporosis.Diabetology & metabolic syndrome · 2023
    Review
  7. Review
  8. Review
  9. 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

4 authors at 1 institution in 1 country.

Jian JieDepartment of Orthopedics, Pukou Branch Hospital of JiangSu Province Hospital (Nanjing Pukou Central Hospital), 166 Shanghe Street, Jiangpu Street, Pukou District, Nanjing, 211800, Jiangsu, China.
Weilin LiDepartment of Orthopedics, Pukou Branch Hospital of JiangSu Province Hospital (Nanjing Pukou Central Hospital), 166 Shanghe Street, Jiangpu Street, Pukou District, Nanjing, 211800, Jiangsu, China.
Guihua WangDepartment of Orthopedics, Pukou Branch Hospital of JiangSu Province Hospital (Nanjing Pukou Central Hospital), 166 Shanghe Street, Jiangpu Street, Pukou District, Nanjing, 211800, Jiangsu, China.
Xiaoming XuDepartment of Orthopedics, Pukou Branch Hospital of JiangSu Province Hospital (Nanjing Pukou Central Hospital), 166 Shanghe Street, Jiangpu Street, Pukou District, Nanjing, 211800, Jiangsu, China. xuxiaomingmxx@outlook.com.ORCID http://orcid.org/0000-0002-7687-2070
Jiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveOsteoporosis is affecting the health of postmenopausal women in the world. In case of that, we explored whether FK-506 could ameliorate osteoporosis by inhibiting the activated CaN/NFAT pathway during oxidative stress.

methodsFirst, the castrated rat model is constructed through the bilateral ovariectomy. Hologic Discovery (S/N 80347) dual-energy X-ray absorptiometry assessed bone mineral density (BMD) implemented at left femur of rats. Next, hematoxylin-eosin (H&E) staining observed and calculated the changes of bone trabecular, mean trabecular plate separation (Tb.Sp), mean trabecular plate thickness (Tb.Th), and bone volume fraction (BV/TV). Then, CCK-8 assay, TUNEL assay, ALP kit and alizarin red staining detected the viability, apoptosis, alkaline phosphatase (ALP) activity, and capacity of mineralization respectively. At last, commercially available kits detected the levels of ROS and SOD in transfected MC3T3-E1 cells and bone tissues, and Western blot analysis detected proteins related to apoptosis and CaN/NFAT pathway.

resultsFK-506 increased the BMD and changes of bone trabecular in female castrated rats. FK-506 inhibited the oxidative stress and apoptosis by suppressing the activated CaN/NFAT pathway. Low dose of FK-506 improved the viability, ALP activity, and mineralization capacity. What's more, it suppressed the apoptosis of H

conclusionFK-506 ameliorates osteoporosis resulted from osteoblastic apoptosis which caused by suppressing the activated CaN/NFAT pathway during oxidative stress.

Indexed as

Alkaline PhosphataseAnimalsApoptosisBone DensityCalcineurinCell LineCell SurvivalFemaleFemurImmunosuppressive AgentsMiceNFATC Transcription FactorsOsteoblastsOsteoporosisOxidative StressRatsAlkaline PhosphataseCalcineurinImmunosuppressive AgentsNFATC Transcription FactorsTacrolimusCaN/NFAT pathwayFK-506Osteoblastic apoptosisOsteoporosisOxidative stress

Identifiers

PMID34165588
OpenAlexW3176050222

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.