Evidence map›Paper›PMID 40682116›Full record

ArticleJournal of translational medicine2025

Sinensetin serves as an AMPK activator to inhibit RANKL-induced osteoclastogenesis via osteoclast cytoskeleton reorganization.

Yijie Gao, Rui Zhou, Xixi Lin, Zhijuan Liu, Yuangang Su, Haoyu Lian, Bin Lin, Xiaofei Ding, Shijie Liao, Xiangde Li and 5 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
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

15 authors.

Yijie Gao *Guangxi Key Laboratory of Regenerative Medicine, Orthopaedics Trauma and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530000, China.
Rui Zhou *Guangxi Key Laboratory of Regenerative Medicine, Orthopaedics Trauma and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530000, China.
Xixi Lin *Department of Orthopedic Surgery, The 909 Hospital, School of Medicine, Xiamen University, 269 Zhanghua Middle Road, Zhangzhou, 363000, China.
Zhijuan LiuGuangxi Key Laboratory of Regenerative Medicine, Orthopaedics Trauma and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530000, China.
Yuangang SuGuangxi Key Laboratory of Regenerative Medicine, Orthopaedics Trauma and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530000, China.
Haoyu LianGuangxi Key Laboratory of Regenerative Medicine, Orthopaedics Trauma and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530000, China.
Bin LinDepartment of Orthopedic Surgery, The 909 Hospital, School of Medicine, Xiamen University, 269 Zhanghua Middle Road, Zhangzhou, 363000, China.
Xiaofei DingGuangxi Key Laboratory of Regenerative Medicine, Orthopaedics Trauma and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530000, China.
Shijie LiaoGuangxi Key Laboratory of Regenerative Medicine, Orthopaedics Trauma and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530000, China.
Xiangde LiGuangxi Key Laboratory of Regenerative Medicine, Orthopaedics Trauma and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530000, China.
Jinmin ZhaoGuangxi Key Laboratory of Regenerative Medicine, Orthopaedics Trauma and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530000, China.
Jiake XuSchool of Biomedical Sciences, the University of Western Australia, Perth, Australia.
Ren XuDepartment of Orthopedic Surgery, The 909 Hospital, School of Medicine, Xiamen University, 269 Zhanghua Middle Road, Zhangzhou, 363000, China. xuren526@xmu.edu.cn.
Qian LiuGuangxi Key Laboratory of Regenerative Medicine, Orthopaedics Trauma and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530000, China. liuqian@gxmu.edu.cn.
Fangming SongGuangxi Key Laboratory of Regenerative Medicine, Orthopaedics Trauma and Hand Surgery, the First Affiliated Hospital of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530000, China. songfangming@gxmu.edu.cn.

Funding

Guangxi Science and Technology Base and Talent Special Project GuikeAD24010038Nanning Qingxiu District Science and Technology Bureau key research and development projects No.2020028National Natural Science Foundation of China 82360175National Natural Science Foundation of China No.82060760Natural Science Foundation of Guangxi Province 2023GXNSFFA026015Shenzhen Medical Research Funds B2302005The Central Guidance for Local Science and Technology Development Projects GuikeZY23055030
6 · The paper itself

Abstract

Osteoporosis is a skeletal condition caused by an excess of osteoclasts, resulting in an imbalance in bone metabolism. Sinensetin (SIN), one of the main ingredients in citrus fruits, provides a variety of pharmacological properties, like antioxidant, but its effects on osteoporosis remains unknown. Herein, we explored at how SIN affected RANKL-induced osteoclastogenesis and ovariectomy (OVX)-induced osteoporotic mice. Our research found that SIN, without compromising cell viability, inhibited RANKL-mediated osteoclastogenesis and the NFATc1 signaling pathway in a concentration-dependent manner. Further, RNA sequencing analysis suggested that the molecular mechanism of SIN inhibitory effect on osteoclasts is related to the cytoskeleton reorganization. The results indicated that SIN prevents the cytoskeleton reorganization of preosteoclasts via the c-Src-mediated PI3K/PAK4/AKT signaling axis. Meanwhile, SIN enhanced the expression of phosphorylation and activity of AMP-activated protein kinase (AMPK) in response to RANKL. Further, SIN targets AMPK to reduce intracellular Reactive oxygen species (ROS) levels, thereby blocking c-Src activation. Finally, we verified that SIN inhibits osteoclast activity, thus preventing OVX-induced bone loss. These findings suggest that SIN serves as an AMPK activator that abrogates RANKL-induced osteoclastogenesis and OVX-induced bone loss via hindering cytoskeleton reorganization.

Indexed as

AMP-Activated Protein KinasesCytoskeletonOsteoclastsOsteogenesisRANK LigandAnimalsBone ResorptionEnzyme ActivationFemaleMiceMice, Inbred C57BLNFATC Transcription FactorsOsteoporosisOvariectomyPhosphatidylinositol 3-KinasesPhosphorylationAMP-Activated Protein KinasesNFATC Transcription FactorsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRANK LigandReactive Oxygen SpeciesAMPKCytoskeleton reorganizationOsteoclastROSSinensetin

Identifiers

PMID40682116
PMCPMC12275404

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.