Evidence map›Paper›PMID 39849573›Full record

ArticleJournal of orthopaedic surgery and research2025

Activation of osteoblast ferroptosis by risperidone accelerates bone loss in mice models of schizophrenia.

Hongyan Fan, Zaihong Yang, Lan Pang, Peifan Li, Changrong Duan, Guangyuan Xia, Lei Zheng

Abstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Hongyan Fan *Guizhou Medical University, Guiyang, China.
Zaihong Yang *Guizhou Medical University, Guiyang, China.
Lan PangGuizhou Medical University, Guiyang, China.
Peifan LiDepartment of Psychiatry, Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Changrong DuanDepartment of Psychiatry, Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Guangyuan XiaDepartment of Psychiatry, Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Lei ZhengGuizhou Medical University, Guiyang, China. zhenglei@gmc.edu.cn.

Funding

National Natural Science Foundation of China 82060651the Doctoral Research Fund of Affiliated Hospital of Guizhou Medical University GYFYBSKY-2021-67
6 · The paper itself

Abstract

backgroundFerroptosis is an iron-dependent regulatory cell death, which plays an essential role in bone loss. This study investigated whether the mechanism of risperidone (RIS)-induced bone loss is related to ferroptosis.

methodsThe schizophrenia mice were induced by administering MK-801. Subsequently, RIS were injected, or ferroptosis inhibitor Ferrostatin-1 (Fer-1) co-injected for 8 weeks. Bone loss of schizophrenia mice were assessed using microCT, H&E staining, ALP staining, ARS staining and WB, respectively. Ferroptosis of schizophrenia mice were detected by Iron Colorimetric Assay Kit and WB, respectively. In addition, ALP staining, ARS staining, and WB were performed to reveal the role of RIS in osteogenic differentiation of MC3T3-E1 and BMSCs cells.

resultsRIS treatment facilitates bone loss in schizophrenia mice and inhibit osteogenic differentiation of MC3T3-E1 and BMSCs cells. Moreover, up-regulated ferroptosis was found in vivo and in vitro after RIS treatment. Interesting, the bone loss and inhibition of osteogenic differentiation induced by RIS in schizophrenia mice were reversed by ferroptosis inhibitor Fer-1.

conclusionFerroptosis induced by RIS aggravates the bone loss of schizophrenia mice via inhibiting osteogenic differentiation.

Indexed as

Antipsychotic AgentsFerroptosisOsteoblastsRisperidoneSchizophreniaAnimalsCell DifferentiationDisease Models, AnimalMaleMiceMice, Inbred C57BLOsteogenesisAntipsychotic AgentsRisperidoneBone lossFerroptosisOsteogenic differentiationRisperidone

Identifiers

PMID39849573
PMCPMC11756223

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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.