Evidence map›Paper›PMID 31625681›Full record

ArticleJournal of cellular and molecular medicine2019

Dexmedetomidine attenuates neuronal injury after spinal cord ischaemia-reperfusion injury by targeting the CNPY2-endoplasmic reticulum stress signalling.

Lina Zhao, Meili Zhai, Xu Yang, Hongjie Guo, Ying Cao, Donghui Wang, Ping Li, Chong Liu

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Appraisal of the Neuroprotective Effect of Dexmedetomidine: A Meta-Analysis.Advances in experimental medicine and biology · 2023
    Pooled it
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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

8 authors at 4 institutions in 1 country.

Lina ZhaoDepartment of Anaesthesiology, Tianjin Hospital, Tianjin, China.
Meili ZhaiDepartment of Anesthesiology, Tianjin Central Hospital of Gynecology Obstetrics, Gynecology Obstetrics Hospital of Nankai University, Tianjin Key Laboratory of human development and reproductive regulation, Tianjin, China.
Xu YangDepartment of medicine, Tianjin Medical College, Tianjin, China.
Hongjie GuoDepartment of Critical Care Medicine, Tianjin 4th Centre Hospital, Tianjin, China.
Ying CaoDepartment of Critical Care Medicine, Tianjin 4th Centre Hospital, Tianjin, China.
Donghui WangDepartment of Medical Imaging, Shanxi Medical University, Taiyuan City, China.
Ping LiDepartment of Anaesthesiology, Tianjin Hospital, Tianjin, China.
Chong LiuDepartment of Anaesthesiology, Central Laboratory, Tianjin 4th Centre Hospital, The Fourth Central Hospital Affiliated to Nankai University, The Fourth Center Clinical College of Tianjin Medical University, Tianjin, China.ORCID 0000-0001-6425-2045
Tianjin Hospital · CNNankai University · CNShanxi Medical University · CNTianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dexmedetomidine (Dex) has been proven to exert protective effects on multiple organs in response to ischaemia-reperfusion injury, but the specific mechanism by which this occurs has not been fully elucidated. The purpose of this study was to investigate whether Dex attenuates spinal cord ischaemia-reperfusion injury (SCIRI) by inhibiting endoplasmic reticulum stress (ERS). Our team established a model of SCIRI and utilized the endoplasmic reticulum agonist thapsigargin. Dex (25 g/kg) was intraperitoneally injected 30 minutes before spinal cord ischaemia. After 45 minutes of ischaemia, the spinal cord was reperfused for 24 hours. To evaluate the neuroprotective effect of Dex on SCIRI, neurological function scores were assessed in rats and apoptosis of spinal cord cells was determined by TUNEL staining. To determine whether the endoplasmic reticulum apoptosis pathway CNPY2-PERK was involved in the neuroprotective mechanism of Dex, the expression levels of related proteins (CNPY2, GRP78, PERK, CHOP, caspase-12, caspase-9 and caspase-3) were detected by western blot analysis and RT-PCR. We observed that Dex significantly increased the neurological function scores after SCIRI and decreased apoptosis of spinal cord cells. The expression of ERS-related apoptosis proteins was significantly increased by SCIRI but was significantly decreased in response to Dex administration. Taken together, the results of this study indicate that Dex may attenuate SCIRI by inhibiting the CNPY2-ERS apoptotic pathway.

Indexed as

AnimalsApoptosisCarrier ProteinsCaspasesDexmedetomidineeIF-2 KinaseEndoplasmic Reticulum Chaperone BiPEndoplasmic Reticulum StressGene ExpressionMaleNeuronsNeuroprotective AgentsRats, Sprague-DawleyReperfusion InjurySignal TransductionSpinal CordCarrier ProteinsCaspasesDexmedetomidineeIF-2 KinaseEndoplasmic Reticulum Chaperone BiPHSPA5 protein, humanMSAP protein, ratNeuroprotective Agentsapoptosisdexmedetomidineendoplasmic reticulumischaemia-reperfusion injuryspinal cord

Identifiers

PMID31625681
PMCPMC6850922
OpenAlexW2980832610

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.