Evidence map›Paper›PMID 36098492›Full record

ArticleOrthopaedic surgery2022

Establishment and Evaluation of a Rat Model of Medial Malleolar Fracture with Vascular Injury.

Jinglai Sun, Qifeng Li, Shuo Wang, Guangpu Wang, Jing Zhao, Huanming Li, Chong Liu, Yifan Shi, Zhigang Li, Hui Yu

Open access · goldAbstract read
In one paragraph

Article in Orthopaedic surgery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Jinglai SunDepartment of Biomedical Engineering, Tianjin Key Laboratory of Biomedical Detecting Techniques and Instruments, Tianjin University, Tianjin, China.
Qifeng LiDepartment of Biomedical Engineering, Tianjin Key Laboratory of Biomedical Detecting Techniques and Instruments, Tianjin University, Tianjin, China.
Shuo WangDepartment of Biomedical Engineering, Tianjin Key Laboratory of Biomedical Detecting Techniques and Instruments, Tianjin University, Tianjin, China.
Guangpu WangDepartment of Biomedical Engineering, Tianjin Key Laboratory of Biomedical Detecting Techniques and Instruments, Tianjin University, Tianjin, China.
Jing ZhaoDepartment of Biomedical Engineering, Tianjin Key Laboratory of Biomedical Detecting Techniques and Instruments, Tianjin University, Tianjin, China.
Huanming LiTianjin Joint Laboratory of Intelligent Medicine, Tianjin 4TH Centre Hospital, Tianjin University, Tianjin, China.
Chong LiuTianjin Joint Laboratory of Intelligent Medicine, Tianjin 4TH Centre Hospital, Tianjin University, Tianjin, China.
Yifan ShiDepartment of Imaging, Tianjin 4TH Centre Hospital, Tianjin, China.
Zhigang LiTianjin Joint Laboratory of Intelligent Medicine, Tianjin 4TH Centre Hospital, Tianjin University, Tianjin, China.ORCID https://orcid.org/0000-0001-6885-9725
Hui YuDepartment of Biomedical Engineering, Tianjin Key Laboratory of Biomedical Detecting Techniques and Instruments, Tianjin University, Tianjin, China.
Tianjin University · CNTianjin Hospital · CN

Funding

Tianjin Science and Technology Committee 18ZXZNSY00240
6 · The paper itself

Abstract

objectiveA stable animal model was needed to study bone non-union caused by insufficient blood supply, the main object of this paper is to develop a medial malleolar fracture model with controllable arterial vascular injuries in rats for revealing the biochemical mechanism of non-union by insufficient blood supply.

methodsA total of 18 rats were randomly divided into three equal groups: the Sham group, the Fracture group, and the Fracture + Vascular group. The animals were subjected to unilateral medial malleolar bone fracture and vascular injury using customized molding equipment. The fracture site was scanned by micro-CT, and vascular injury was evaluated by laser Doppler flowmetry (LDF) 24 h after modeling. Histological examination (HE), alkaline phosphatase (ALP) and tartrate-resistant acid phosphatase (TRAP) staining, immunohistochemistry and immunofluorescence were conducted on the medial malleolar fracture tissues of three rats randomly selected from each group 24 h after modeling. Subsequently, to further confirm the success of fracture modeling, the fracture sites of three other rats in each group underwent micro-CT scanning again 6 weeks after surgery.

resultsThe results of a 24 h micro-CT showed that all rats used to create the fracture models showed controlled injury of the medial malleolus. The model was stable, and the satisfaction of the homemade equipment agreed with the expectation. LDF showed that the blood flow of rats in the Fracture + Vascular group decreased significantly 24 h after fracture injury, while collateral blood flow perfusion increased by 50% on average. The results of HE, ALP and TRAP staining in the medial malleolus showed that the number of osteoblasts (OBs) and osteoclasts (OCs) in the Fracture group increased significantly, but the number of OBs and OCs in the Fracture + Vascular group decreased sharply relative to the number in the Sham group 24 h later. Furthermore, immunohistochemistry and immunofluorescence results showed that the number of neovessels in the Fracture group was significantly increased, while the number of neovessels in the Fracture + Vascular group was significantly decreased, which was consistent with the above results. After 6 weeks of modeling, the micro-CT results showed that the fractures in the Fracture group had healed substantially, while those in the Fracture + Vascular group had not.

conclusionThis study provided a reproducible and stable experimental animal model for medial malleolar fractures with arterial injury.

Indexed as

Ankle FracturesVascular System InjuriesAlkaline PhosphataseAnimalsFracture Fixation, InternalRatsRetrospective StudiesTartrate-Resistant Acid PhosphataseAlkaline PhosphataseTartrate-Resistant Acid PhosphataseAnimal modelAnkleArterial vascularFractureRat

Identifiers

PMID36098492
PMCPMC9531110
OpenAlexW4295366945

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.