Evidence map›Paper›PMID 35980287›Full record

ArticleJournal of tissue engineering and regenerative medicine2022

The effect of resolvin D1 on bone regeneration in a rat calvarial defect model.

Xiaofeng Jiang, Jing Liu, Si Li, Yingfei Qiu, Xiaoli Wang, Xiaoli He, Torbjørn Ø Pedersen, Kamal Mustafa, Ying Xue, Manal Mustafa and 2 more

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Journal of tissue engineering and regenerative medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
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

13 citing papers in PubMed, 18 citations in OpenAlex.

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  13. The effect of resolvin D1 on bone regeneration in a rat calvarial defect model.Journal of tissue engineering and regenerative medicine · 2022
    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

12 authors at 5 institutions in 3 countries.

Xiaofeng JiangSchool/Hospital of Stomatology, Lanzhou University, Lanzhou, China.
Jing LiuSchool/Hospital of Stomatology, Lanzhou University, Lanzhou, China.
Si LiSchool/Hospital of Stomatology, Lanzhou University, Lanzhou, China.
Yingfei QiuSchool/Hospital of Stomatology, Lanzhou University, Lanzhou, China.
Xiaoli WangSchool/Hospital of Stomatology, Lanzhou University, Lanzhou, China.
Xiaoli HeSchool/Hospital of Stomatology, Lanzhou University, Lanzhou, China.
Torbjørn Ø PedersenDepartment of Clinical Dentistry, Faculty of Medicine, University of Bergen, Bergen, Norway.
Kamal MustafaDepartment of Clinical Dentistry, Faculty of Medicine, University of Bergen, Bergen, Norway.
Ying XueDepartment of Clinical Dentistry, Faculty of Medicine, University of Bergen, Bergen, Norway.
Manal MustafaOral Health Centre of Expertise in Western Norway, Bergen, Norway.
Alpdogan KantarciThe Forsyth Institute, Cambridge, Massachusetts, USA.
Zhe XingSchool/Hospital of Stomatology, Lanzhou University, Lanzhou, China.ORCID 0000-0002-7419-2012
Lanzhou University · CNUniversity of Bergen · NOHarvard University · USHaukeland University Hospital · NOWestern Norway University of Applied Sciences · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resolvin D1 (RvD1) is a pro-resolving lipid mediator of inflammation, endogenously synthesized from omega-3 docosahexaenoic acid. The purpose of this study was to investigate the effect of RvD1 on bone regeneration using a rat calvarial defect model. Collagen 3D nanopore scaffold (COL) and Pluronic F127 hydrogel (F127) incorporated with RvD1 (RvD1-COL-F127 group) or COL and F127 (COL-F127 group) were implanted in symmetrical calvarial defects. After implantation, RvD1 was administrated subcutaneously every 7 days for 4 weeks. The rats were sacrificed at weeks 1 and 8 post-implantation. Tissue samples were analyzed by real-time reverse transcriptase-polymerase chain reaction and histology at week 1. Radiographical and histological analyses were done at week 8. At week 1, calvarial defects treated with RvD1 exhibited decreased numbers of inflammatory cells and tartrate-resistant acid phosphatase (TRAP) positive cells, greater numbers of newly formed blood vessels, upregulated gene expression of vascular endothelial growth factor and alkaline phosphatase, and downregulated gene expression of receptor activator of nuclear factor-κB ligand, interleukin-1β and tumor necrosis factor-α. At week 8, the radiographical results showed that osteoid area fraction of the RvD1-COL-F127 group was higher than that of the COL-F127 group, and histological examination exhibited enhanced osteoid formation and newly formed blood vessels in the RvD1-COL-F127 group. In conclusion, this study showed that RvD1 enhanced bone formation and vascularization in rat calvarial defects.

Indexed as

Docosahexaenoic AcidsSkullVascular Endothelial Growth Factor AAnimalsBone RegenerationPolyethylenesPolypropylenesRatsDocosahexaenoic AcidsPolyethylenesPolypropylenesresolvin D1UCON 50-HB-5100Vascular Endothelial Growth Factor Aosteogenesisresolvin D1vascularization

Identifiers

PMID35980287
OpenAlexW4292202455

What OpenQuestion holds

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Read underepoch 390

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.