Evidence map›Paper›PMID 38326818›Full record

ArticleJournal of orthopaedic surgery and research2024

Icariin promotes bone marrow mesenchymal stem cells osteogenic differentiation via the mTOR/autophagy pathway to improve ketogenic diet-associated osteoporosis.

Wei Liu, Shouyu Xiang, Yingcong Wu, Dinghao Zhang, Chuhai Xie, Hailan Hu, Qi Liu

Open access · goldAbstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
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  10. Frontiers in pharmacology · 2025
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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.

Wei Liu *Division of Spinal Surgery, Department of Orthopedics, The Second Affiliated Hospital of Guangzhou Medical University, No.250, Changgang East Road, Guangzhou, 510260, Guangdong, China.
Shouyu Xiang *Division of Spinal Surgery, Department of Orthopedics, The Second Affiliated Hospital of Guangzhou Medical University, No.250, Changgang East Road, Guangzhou, 510260, Guangdong, China.
Yingcong Wu *Division of Spinal Surgery, Department of Orthopedics, The Second Affiliated Hospital of Guangzhou Medical University, No.250, Changgang East Road, Guangzhou, 510260, Guangdong, China.
Dinghao ZhangDivision of Spinal Surgery, Department of Orthopedics, The Second Affiliated Hospital of Guangzhou Medical University, No.250, Changgang East Road, Guangzhou, 510260, Guangdong, China.
Chuhai XieDivision of Spinal Surgery, Department of Orthopedics, The Second Affiliated Hospital of Guangzhou Medical University, No.250, Changgang East Road, Guangzhou, 510260, Guangdong, China.
Hailan HuDivision of Spinal Surgery, Department of Orthopedics, The Second Affiliated Hospital of Guangzhou Medical University, No.250, Changgang East Road, Guangzhou, 510260, Guangdong, China. Lanhu75@163.com.
Qi LiuDivision of Spinal Surgery, Department of Orthopedics, The Second Affiliated Hospital of Guangzhou Medical University, No.250, Changgang East Road, Guangzhou, 510260, Guangdong, China. 413440129@qq.com.
Second Affiliated Hospital of Guangzhou Medical University · CNGuangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIcariin, a traditional Chinese medicine, has demonstrated anti-osteoporotic properties in ovariectomized mice. However, its effectiveness in preventing bone loss induced by ketogenic diet (KD), which mimics osteoporosis in human, remains unexplored. This study aims to investigate icariin's impact on KD-induced bone loss in mice.

methodsThirty mice were divided into: sham, KD, and KD + icariin groups. Post a 12-week intervention, evaluation including bone microstructures, serum concentrations of tartrate-resistant acid phosphatase (TRAP) and bone-specific alkaline phosphatase (ALP), and femoral tissue expression levels of osteocalcin (OCN) and TRAP. The expression levels of mammalian target of rapamycin (mTOR), ALP, peroxisome proliferator-activated receptor gamma (PPAR-γ), phosphorylated mTOR (p-mTOR), and the autophagy adaptor protein (p62) were also analyzed. Alizarin granule deposition and cellular ALP levels were measured following the induction of bone marrow mesenchymal stem cells (BMSCs) into osteogenesis.

resultsThe study found that KD significantly impaired BMSCs' osteogenic differentiation, leading to bone loss. Icariin notably increased bone mass, stimulated osteogenesis, and reduced cancellous bone loss. In the KD + icariin group, measures such as bone tissue density (TMD), bone volume fraction (BV/TV), trabecular number (Tb.N), and trabecular thickness (Tb.Th) were significantly higher than in the KD group. Additionally, bone trabecular separation (Tb.Sp) was markedly lower in the KD + icariin group. Moreover, icariin increased OCN and ALP levels while suppressing PPAR-γ, TRAP, p62, and p-mTOR. In cellular studies, icariin encouraged osteogenic development in BMSCs under KD conditions.

conclusionsIcariin effectively counteracts bone thinning and improves bone microstructure. Its mechanism likely involves stimulating BMSCs osteogenic differentiation and inhibiting bone resorption, potentially through mTOR downregulation. These findings suggest icariin's potential as an alternative treatment for KD-induced bone loss.

Indexed as

Bone Diseases, MetabolicDiet, KetogenicFlavonoidsMesenchymal Stem CellsOsteoporosisAnimalsAutophagyBone Marrow CellsCell DifferentiationCells, CulturedHumansMammalsMiceOsteogenesisPeroxisome Proliferator-Activated ReceptorsTOR Serine-Threonine KinasesFlavonoidsicariinPeroxisome Proliferator-Activated ReceptorsTOR Serine-Threonine KinasesAutophagyIcariinKetogenic dietmTOROsteoporosis

Identifiers

PMID38326818
PMCPMC10851475
OpenAlexW4391599965

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.