Evidence map›Paper›PMID 32253606›Full record

ArticleMedical molecular morphology2021

Hesperetin alleviated glucocorticoid-induced inhibition of osteogenic differentiation of BMSCs through regulating the ERK signaling pathway.

Ling Liu, Jie Zheng, YaZhen Yang, Lingjuan Ni, Hongyu Chen, Dongrong Yu

Abstract read
PubMed Publisher
In one paragraph

Article in Medical molecular morphology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Nutraceuticals in osteoporosis prevention.Frontiers in nutrition · 2024
    Review
  7. 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 1 institution in 1 country.

Ling LiuDepartment of Nephrology, Hangzhou Hospital of Traditional Chinese Medicine, Tiyuchang Road 453, Hangzhou, 310007, Zhejiang, People's Republic of China.
Jie ZhengDepartment of Nephrology, Hangzhou Hospital of Traditional Chinese Medicine, Tiyuchang Road 453, Hangzhou, 310007, Zhejiang, People's Republic of China.
YaZhen YangDepartment of Nephrology, Hangzhou Hospital of Traditional Chinese Medicine, Tiyuchang Road 453, Hangzhou, 310007, Zhejiang, People's Republic of China.
Lingjuan NiDepartment of Nephrology, Hangzhou Hospital of Traditional Chinese Medicine, Tiyuchang Road 453, Hangzhou, 310007, Zhejiang, People's Republic of China.
Hongyu ChenDepartment of Nephrology, Hangzhou Hospital of Traditional Chinese Medicine, Tiyuchang Road 453, Hangzhou, 310007, Zhejiang, People's Republic of China. chenhongyu222@126.com.
Dongrong YuDepartment of Nephrology, Hangzhou Hospital of Traditional Chinese Medicine, Tiyuchang Road 453, Hangzhou, 310007, Zhejiang, People's Republic of China. yudongrong2016@126.com.
Hangzhou Hospital of Traditional Chinese Medicine · CN

Funding

Hangzhou Science and Technology Bureau (CN) 20160533B61Natural Science Foundation of Zhejiang Province LQ18H050005Zhejiang Province Public Welfare Technology Application Research Project (CN) 2018KY613Zhejiang Traditional Chinese Medicine Administration 2019ZA086
6 · The paper itself

Abstract

The objective of this study is to investigate the protective role of hesperetin for the glucocorticoid-induced osteoporosis (GIOP) and related mechanisms. In this study, we investigated the protective effects of hesperetin on dexamethasone (DEX)-induced osteogenic inhibition in bone marrow mesenchymal stem cells (BMSCs). The mineralization, real-time quantitative polymerase chain reaction assays (RT-qPCR), immunofluorescence and western blot were used to assess the protective effects of hesperetin in DEX-treated BMSCs during osteogenic differentiation. Our results showed that hesperetin promoted alkaline phosphatase (ALP) activity and the mineralization in DEX-treated BMSCs during osteogenic differentiation. The expression of osteogenic mRNA and proteins further confirmed the protective effect of hesperetin in DEX-treated BMSCs. Furthermore, hesperetin activated ERK signal pathway in DEX-treated BMSCs. ERK inhibitor U0126 could abolish the protective effect of hesperein in DEX-treated BMSCs. In conclusion, our study demonstrated that hesperetin alleviated glucocorticoid-induced inhibition of osteogenic differentiation through ERK signal pathway in BMSCs. It may be a potential therapeutic agent for protecting against glucocorticoid-induced osteoporosis.

Indexed as

ButadienesCell DifferentiationDexamethasoneExtracellular Signal-Regulated MAP KinasesGlucocorticoidsHesperidinHumansMAP Kinase Signaling SystemMesenchymal Stem CellsNitrilesOsteogenesisOsteoporosisPrimary Cell CultureButadienesDexamethasoneExtracellular Signal-Regulated MAP KinasesGlucocorticoidshesperetinHesperidinNitrilesU 0126Bone marrow mesenchymal stem cellsERKGlucocorticoid-induced osteoporosisHesperetin

Identifiers

PMID32253606
OpenAlexW3014759818

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.