Evidence map›Paper›PMID 39975419›Full record

ArticleInternational journal of nanomedicine2025

Ancient Medicinal Insect

Jiaxu Lu, Jiaxian Chen, Youping Jiang, Yuanyuan Liu, Sheng Yu, Zhen Shi, Peicong Chen, Hao Lin, Peng Li

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Discovery of vasodilatory effects of NaActa pharmacologica Sinica · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. 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

9 authors.

Jiaxu Lu *Stem Cell Research and Cellular Therapy Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, People's Republic of China.
Jiaxian Chen *Orthopedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, People's Republic of China.
Youping JiangStem Cell Research and Cellular Therapy Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, People's Republic of China.
Yuanyuan LiuStem Cell Research and Cellular Therapy Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, People's Republic of China.
Sheng YuOrthopedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, People's Republic of China.
Zhen ShiOrthopedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, People's Republic of China.
Peicong ChenOrthopedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, People's Republic of China.
Hao LinOrthopedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, People's Republic of China.
Peng LiStem Cell Research and Cellular Therapy Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, People's Republic of China.ORCID 0000-0003-1695-512X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Osteoporosis, a critical public health challenge, is marked by skeletal deformities and heightened fracture risk. Methods: We isolated extracellular vesicle (EV)-like particles from SP (SP-EVLP) using differential velocity centrifugation and investigated their effects on human bone marrow stromal cells (hBMSCs) in vitro. We utilized CCK-8, Alkaline phosphatase (ALP) and alizarin red staining (ARS), RNA-seq, bioinformatics, immunofluorescence, and Western blot to elucidate the osteoprotective role and mechanisms of SP-EVLP. The therapeutic potential of SP-EVLP was evaluated in an ovariectomized (OVX) rat model, a standard model for osteoporosis, by encapsulating them in enteric-coated capsules. Results: SP-EVLP were successfully isolated and characterized, and they were shown to be effectively internalized by hBMSCs, enhancing osteogenic differentiation. In the OVX rat model, SP-EVLP encapsulated in enteric-coated capsules significantly increased bone mass, indicating a robust osteoprotective effect. Further mechanistic studies revealed that SP-EVLP promotes osteoblast proliferation by activating melatonin-induced autophagy, a pathway that may improve osteoporotic conditions. Conclusion: Our results establish SP-EVLP as a promising therapeutic candidate for osteoporosis. The activation of melatonin-induced autophagy by SP-EVLP suggests a molecular mechanism for its osteoprotective effects, opening new possibilities for osteoporosis treatment development.

Indexed as

AutophagyExtracellular VesiclesMelatoninOsteogenesisOsteoporosisAnimalsCell DifferentiationCells, CulturedDisease Models, AnimalFemaleHumansMedicine, Chinese TraditionalMesenchymal Stem CellsOvariectomyRatsRats, Sprague-DawleyMelatoninautophagyextracellular vesicles (EV)-like particlesmelatoninOsteoporosisSteleophaga plancyi (Boleny)

Identifiers

PMID39975419
PMCPMC11835776

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.