Evidence map›Paper›PMID 42827972›Full record

ReviewJournal of inflammation research2026

Icariin as a Metabolic Regulator of Bone Marrow Mesenchymal Stem Cells: Mechanisms and Therapeutic Implications to Bone Homeostasis.

Kaiyue Zhang, Jiaming Sun, Zhenming Yu, Yuan Gao, Yuwei Zhao, Hao Li, Yufang He, Minlun Nan

Abstract readReview
In one paragraph

Review in Journal of inflammation research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Kaiyue ZhangInstitute of Chinese Materia Medica Chemistry, Jilin Academy of Chinese Medical Sciences, Changchun, 130012, People's Republic of China.ORCID 0009-0001-2458-0789
Jiaming SunJilin Ginseng Academy, Changchun University of Chinese Medicine, Changchun, 130117, People's Republic of China.
Zhenming YuDepartment of Traditional Chinese Medicine Research, China State Institute of Pharmaceutical Industry, Shanghai, 201203, People's Republic of China.
Yuan GaoInstitute of Chinese Materia Medica Chemistry, Jilin Academy of Chinese Medical Sciences, Changchun, 130012, People's Republic of China.
Yuwei ZhaoCollege of Health Management, Changchun University of Chinese Medicine, Changchun, 130117, People's Republic of China.
Hao LiCollege of Health Management, Changchun University of Chinese Medicine, Changchun, 130117, People's Republic of China.
Yufang HeCollege of Health Management, Changchun University of Chinese Medicine, Changchun, 130117, People's Republic of China.
Minlun NanInstitute of Chinese Materia Medica Chemistry, Jilin Academy of Chinese Medical Sciences, Changchun, 130012, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epimedium and its principal bioactive flavonoid, Icariin (ICA), are recognized as significant regulators of bone metabolism. ICA is well-documented for its ability to enhance osteogenesis and suppress osteoclastogenesis, yet its capacity to influence cellular metabolic pathways is a burgeoning field of investigation. The differentiation of bone marrow mesenchymal stem cells (BMSC) into either osteogenic or adipogenic lineages is intricately associated with intrinsic metabolic alterations, the dysregulation of which is a pivotal factor in the pathogenesis of osteoporosis. This review, conducted following a systematic literature search and quality assessment utilizing Joanna Briggs Institute (JBI) tools, examines the potential of ICA to modulate the osteogenic-adipogenic equilibrium of BMSC. Given that much of the extant evidence concerning direct metabolic reprogramming is indirect, we integrate insights from recent molecular studies to propose mechanisms by which ICA may interact with critical BMSC pathways, particularly glycolysis and fatty acid metabolism. Ultimately, we assess the therapeutic prospects of modulating BMSC metabolism with ICA, and we identify prospective directions for its clinical application in the management of bone disorders.

Indexed as

BMSCicariinmetabolic reprogrammingmitochondrial functionosteogenesis

Identifiers

PMID42827972
PMCPMC13632622

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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.