Evidence map›Paper›PMID 36624462›Full record

ArticleJournal of orthopaedic surgery and research2023

Study on the treatment of postmenopausal osteoporosis with quercetin in Liuwei Dihuang Pill based on network pharmacology.

Fuping Zhu, Wuping Li, Linhua Wang, Bing Dai, Zongyi Liu, Hang Wu, Ting Deng

Open access · goldAbstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2023. 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
2.2field-weighted citation impact, top 13% 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, 14 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Fuping ZhuDepartment of Foot and Ankle Orthopedics, The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine, Changsha, China.
Wuping LiDepartment of Foot and Ankle Orthopedics, The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine, Changsha, China.
Linhua WangDepartment of Extremities and Arthrosis, The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine, Changsha, China.
Bing DaiDepartment of Pharmacy, The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine, Changsha, China.
Zongyi LiuDepartment of Foot and Ankle Orthopedics, The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine, Changsha, China.
Hang WuDepartment of Foot and Ankle Orthopedics, The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine, Changsha, China.
Ting DengClinical Nursing Teaching and Research Section, The Second Xiangya Hospital of Central South University, No. 139, Renmin Road, Furong District, Changsha, Hunan, China. tinadt@139.com.
First Affiliated Hospital of Hunan University of Traditional Chinese Medicine · CNCentral South University · CN

Funding

Key Project of Hunan Provincial Department of Education 21A0227Provincial Central Administration Project E2022008
6 · The paper itself

Abstract

backgroundLiuwei Dihuang Pill (LP) was verified to alleviate postmenopausal osteoporosis (PMOP) development. Nevertheless, the major constituent of LP and the related network pharmacology study remain unexplored.

methodsProtein-protein interaction was established to identify the downstream target of LP in PMOP, and the related signaling pathway was investigated by bioinformatics analysis. MC3T3-E1 cells were added to ferric ammonium citrate (FAC) to mimic osteoporosis in vitro. The osteoblasts were identified by Alizarin red staining. Western blot was applied to evaluate protein levels. In addition, Cell Counting Kit-8 (CCK8) assay was applied to assess cell viability, and cell apoptosis was assessed by flow cytometry.

resultsQuercetin was the major constituent of LP. In addition, quercetin significantly reversed FAC-induced inhibition of osteogenic differentiation in MC3T3-E1 cells. In addition, quercetin notably abolished the FAC-induced upregulation of Bax, Caspase-3, FOS, JUN, TGFB1 and PPARD. In contrast, Bcl-2, p-mTOR/mTOR, p-AKT/AKT and p-PI3K/PI3K levels in MC3T3-E1 cells were reduced by FAC, which was restored by quercetin. Meanwhile, FAC notably inhibited the viability of MC3T3-E1 cells via inducing apoptosis, but this impact was abolished by quercetin. Furthermore, quercetin could reverse pcDNA3.1-FOS-mediated growth of FAC-treated osteoblasts by mediating PI3K/AKT/mTOR signaling.

conclusionQuercetin alleviated the progression of PMOP via activation of PI3K/AKT/mTOR signaling. Hence, this study would shed novel insights into discovering new methods against PMOP.

Indexed as

Osteoporosis, PostmenopausalProto-Oncogene Proteins c-aktQuercetinAnimalsCell LineDrugs, Chinese HerbalFemaleMiceNetwork PharmacologyOsteoblastsOsteogenesisPhosphatidylinositol 3-KinasesTOR Serine-Threonine KinasesDrugs, Chinese HerbalLiuwei Dihuang DecoctionPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktQuercetinTOR Serine-Threonine KinasesPI3K/AKT signalingPostmenopausal osteoporosisPPIQuercetin

Identifiers

PMID36624462
PMCPMC9827666
OpenAlexW4313891481

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.