Evidence map›Paper›PMID 39476282›Full record

ArticleIn vitro cellular & developmental biology. Animal2025

The inhibitory effect of salidroside on RANKL-induced osteoclast formation via NFκB suppression.

Adilsaikhan Mendjargal, Shijir Narmandakh, Munkhjargal Zinamyadar, Egshiglen Amartuvshin, Juramt Bold, Nandin Garmaa, Enebish Sundui, Amgalanbaatar Dorjkhuu, Avirmed Amgalanbaatar, Erdenezaya Odkhuu

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Article in In vitro cellular & developmental biology. Animal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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4 · The record

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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

10 authors.

Adilsaikhan MendjargalMongolia Japan Hospital, Mongolian National University of Medical Sciences, Botanic garden, Ulaanbaatar, 13270, Mongolia.
Shijir NarmandakhMongolian Society for Human Anatomy, Ulaanbaatar, Mongolia.
Munkhjargal ZinamyadarMongolian Society for Human Anatomy, Ulaanbaatar, Mongolia.
Egshiglen AmartuvshinMongolian Society for Human Anatomy, Ulaanbaatar, Mongolia.
Juramt BoldMongolian Society for Human Anatomy, Ulaanbaatar, Mongolia.
Nandin GarmaaMongolian Society for Human Anatomy, Ulaanbaatar, Mongolia.
Enebish SunduiMongolian Society for Human Anatomy, Ulaanbaatar, Mongolia.
Amgalanbaatar DorjkhuuMongolian Society for Human Anatomy, Ulaanbaatar, Mongolia.
Avirmed AmgalanbaatarMongolian Society for Human Anatomy, Ulaanbaatar, Mongolia.
Erdenezaya OdkhuuMongolian Society for Human Anatomy, Ulaanbaatar, Mongolia. erdenezaya@mnums.edu.mn.ORCID http://orcid.org/0000-0002-5731-0726

Funding

Mongolian National University of Medical Sciences #2020/1-16
6 · The paper itself

Abstract

Bone fractures are a prevalent clinical issue, and recent studies highlighted the promising potential of natural bone healing agents in enhancing fracture repair and regeneration. The regulatory interaction mechanism between osteoblasts and osteoclasts is crucial for bone cell biology and bone disease. In Mongolian medicine, people have used the Rhodiola rosea (R. rosea) extract to accelerate bone healing in bone fractures. Salidroside is a bioactive compound of R. rosea. Salidroside is known to regulate bone metabolism and inhibit the activation of osteoclast cells, but how it affects the differentiation of osteoclasts is unknown. We examined the effect of R. rosea extract and its bioactive compound salidroside on the RANKL-induced osteoclast formation in RAW 264.7 cells. The present study observed that salidroside directly inhibits RANKL-induced TRAP-positive osteoclast formation. Immunoblotting analysis revealed that salidroside inhibited the expression of c-Fos and NFATc1, osteoclastogenic key transcription factors, by suppressing late activation of p65 NFκB. Further, the ethanol extracts of R. rosea significantly reduced the RANKL-induced osteoclasts in a dose-dependent manner. In conclusion, salidroside inhibits RANKL-induced osteoclast formation via suppressing the NFκB/c-Fos/NFATc1 signalling pathway. R. rosea, a primary source of salidroside, is helpful for bone healing via its inhibitory effect on osteoclast formation.

Indexed as

GlucosidesNF-kappa BOsteoclastsPhenolsRANK LigandAnimalsCell DifferentiationMiceNFATC Transcription FactorsOsteogenesisPlant ExtractsProto-Oncogene Proteins c-fosRAW 264.7 CellsRhodiolaSignal TransductionGlucosidesNFATC Transcription FactorsNF-kappa BPhenolsPlant ExtractsProto-Oncogene Proteins c-fosRANK LigandrhodiolosideNFATc1OsteoclastRhodiola roseaSalidroside

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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 Socratic graph.