Evidence map›Paper›PMID 35993796›Full record

ArticleThe journal of spinal cord medicine2024

Differences in the expression of myelopathy in a rat model of chronic spinal cord compression.

Masataka Miura, Takeo Furuya, Masayuki Hashimoto, Yuki Shiratani, Takaki Inoue, Atsushi Yunde, Sho Okimatsu, Hiroaki Hosokawa, Satoshi Maki, Seiji Ohtori

Open access · greenAbstract read
In one paragraph

Article in The journal of spinal cord medicine, 2024. 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
0.3field-weighted citation impact, top 44% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

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

10 authors at 2 institutions in 1 country.

Masataka MiuraDepartment of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0002-8344-1316
Takeo FuruyaDepartment of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0002-5378-940X
Masayuki HashimotoDepartment of Orthopaedic Surgery, Chiba Medical Center, Chiba, Japan.ORCID 0000-0002-6710-4918
Yuki ShirataniDepartment of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0003-4832-6491
Takaki InoueDepartment of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0002-5096-2350
Atsushi YundeDepartment of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0003-3202-056X
Sho OkimatsuDepartment of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0003-0849-7931
Hiroaki HosokawaDepartment of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0002-5472-910X
Satoshi MakiDepartment of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0002-6809-3771
Seiji OhtoriDepartment of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0001-5738-6184
Chiba University · JPTeikyo University Chiba Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CONTEXT/

objectiveThe degree of spinal cord compression does not always parallel neurological symptoms. We considered that some compensatory neuroprotective mechanism underlies the expression of this neurological phenotype. Oxygen-regulated-protein 150 (ORP150) is neuroprotective and expressed in neurons in response to neuronal ischemia. We sought to elucidate whether ORP150 expression is associated with the severity and variation of neurological recovery in our rat model of chronic spinal cord compression.

methodsWe made a rat model of chronic spinal cord compression inserting an expandable water-absorbing polyurethane sheet. A neurological behavioral assessment of the severity of paralysis was performed for 10 weeks postoperatively. The rat model was defined as two groups: a myelopathy group with decreased locomotor function and an asymptomatic group. At 10 weeks postoperatively, the spinal cord of the cervical segment was resected for histology and qPCR.

resultsSlowly progressive paralysis appeared at 5-10 weeks postoperatively in 53% of the rats with spinal cord compression. The asymptomatic group had no histological changes indicative of myelopathy. Histology and qPCR showed increased expression of ORP150 in the asymptomatic group, but the ratio of ORP150-positive neuron in the two groups was not significantly different.

conclusionThe expression of ORP150 in neurons associated with spinal cord compression suggested that the spinal cord was under ischemic stress due to compression, but relation to the development of myelopathy was unclear. The results suggested that some other compensatory mechanisms may exist in response to spinal cord compression in asymptomatic rats.

Indexed as

Disease Models, AnimalSpinal Cord CompressionAnimalsMaleNeuronsRatsRats, Sprague-DawleySpinal CordCervical myelopathySpinal cord compressionSpinal cord ischemiaWord

Identifiers

PMID35993796
PMCPMC11044740
OpenAlexW4292608990

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.