Evidence map›Paper›PMID 42576484›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2026

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Ruoxi Zheng, Lihua Xie, Xiaobin Huang, Jirong Ge

Abstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 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

4 authors.

Ruoxi ZhengMinistry of Education Key Laboratory of Orthopedics and Traumatology of Traditional Chinese Medicine and Rehabilitation, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, China.
Lihua XieFujian Key Laboratory of Integrated Traditional Chinese and Western Medicine for Osteoporosis Prevention and Treatment (Fujian Academy of Chinese Medical Sciences, Rehabilitation Hospital Affiliated to Fujian University of Traditional Chinese Medicine), Fuzhou 350001, China.
Xiaobin HuangFujian Key Laboratory of Integrated Traditional Chinese and Western Medicine for Osteoporosis Prevention and Treatment (Fujian Academy of Chinese Medical Sciences, Rehabilitation Hospital Affiliated to Fujian University of Traditional Chinese Medicine), Fuzhou 350001, China.
Jirong GeFujian Key Laboratory of Integrated Traditional Chinese and Western Medicine for Osteoporosis Prevention and Treatment (Fujian Academy of Chinese Medical Sciences, Rehabilitation Hospital Affiliated to Fujian University of Traditional Chinese Medicine), Fuzhou 350001, China.

Funding

National Natural Science Foundation of China 82374483 and 82274563
6 · The paper itself

Abstract

objectivesTo explore the mechanism of

methodsThirty female C57BL/6 mice were randomized equally into sham-operated group, PMOP model group, and LWDHW treatment group. The mice in the latter two groups underwent ovariectomy to simulate PMOP, followed by gavage of normal saline and LWDHW (twice daily) for 60 days, respectively. Bone mineral density (BMD) of the mice was detected, and TRAP staining was used to observe osteoclast and osteoclast maturation in the tibia tissue. In RANKL-induced RAW264.7 cells with or without lentivirus-mediated CLCF1 knockdown, the effects of incubation with normal rat serum or LWDHW-medicated rat serum on cell membrane fusion rate and F-actin loop formation were observed using immunofluorescence staining with phalloidin peptide; the mRNA and protein expressions of CLCF1, NFATc1, DC-STAMP, OC-STAMP and ATP6V0D2 were detected using RT-qPCR and Western blotting.

resultsIn PMOP mice, LWDHW treatment significantly increased BMD, reduced osteoclast maturation, osteoclast membrane fusion rate, and F-actin ring formation, upregulated the mRNA and protein expressions of CLCF1 in tibial tissues, and lowered the expressions of NFATc1, DC-STAMP, OC-STAMP and ATP6V0D2. In RANKL-induced RAW264.7 cells with CLCF1 knockdown, treatment with LWDHW-medicated rat serum significantly decreased osteoclast membrane fusion rate, F-actin ring formation, and the expressions of NFATc1, DC-STAMP, OC-STAMP and ATP6V0D2.

conclusionsLWDHW improves PMOP in mice by regulating osteoclast membrane fusion through upregulating CLCF1 expression and downregulating NFATc1, DC-STAMP, OC-STAMP and ATP6V0D2 expressions.

Indexed as

Chloride ChannelsDrugs, Chinese HerbalNFATC Transcription FactorsOsteoclastsOsteoporosis, PostmenopausalAnimalsBone DensityFemaleMiceMice, Inbred C57BLRANK LigandRAW 264.7 CellsSignal TransductionChloride ChannelsDrugs, Chinese HerbalLiuwei Dihuang DecoctionNfatc1 protein, mouseNFATC Transcription FactorsRANK LigandLiuwei Dihuang Pillmembrane fusionosteoclastspostmenopausal osteoporosis

Identifiers

PMID42576484
PMCPMC13458560

What OpenQuestion holds

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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 OpenQuestion graph.