Evidence map›Paper›PMID 29621970›Full record

ArticleBMC anesthesiology2018

The interplay of BDNF-TrkB with NMDA receptor in propofol-induced cognition dysfunction : Mechanism for the effects of propofol on cognitive function.

Junfei Zhou, Fang Wang, Jun Zhang, Jianfeng Li, Li Ma, Tieli Dong, Zhigang Zhuang

Open access · goldAbstract read
In one paragraph

Article in BMC anesthesiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 23 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

7 authors at 2 institutions in 1 country.

Junfei ZhouDepartment of Anesthesiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450003, China.
Fang WangDepartment of Pain, The Second Affiliated Hospital of Zhengzhou University, College of Medicine, No. 2 Jingba Road, Zhengzhou, 450003, China.
Jun ZhangDepartment of Pain, The Second Affiliated Hospital of Zhengzhou University, College of Medicine, No. 2 Jingba Road, Zhengzhou, 450003, China.
Jianfeng LiDepartment of Pain, The Second Affiliated Hospital of Zhengzhou University, College of Medicine, No. 2 Jingba Road, Zhengzhou, 450003, China.
Li MaDepartment of Pain, The Second Affiliated Hospital of Zhengzhou University, College of Medicine, No. 2 Jingba Road, Zhengzhou, 450003, China.
Tieli DongDepartment of Anesthesiology, The Second Affiliated Hospital of Zhengzhou University, College of Medicine, No. 2 Jingba Road, Zhengzhou, 450003, China. mrdongtl@sohu.com.ORCID 0000-0002-6154-543X
Zhigang ZhuangDepartment of Pain, The Second Affiliated Hospital of Zhengzhou University, College of Medicine, No. 2 Jingba Road, Zhengzhou, 450003, China. zhuangzg055@sohu.com.
Second Affiliated Hospital of Zhengzhou University · CNFirst Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of the present study was to verify whether propofol impaired learning and memory through the interplay of N-methyl-D-aspartate (NMDA) receptor with brain-derived neurotrophic factor (BDNF)-tyrosine kinase B (TrkB) signaling pathway.

methods120 Sprague-Dawley (SD) rats were randomly assigned into eight groups. Experimental drugs including saline, intralipid, propofol, N-methyl-D-aspartate (NMDA), 7,8-dihydroxyflavone (7,8-DHF), K252a and MK-801. Spatial learning and memory of rats were tested by the Morris water maze (MWM) test. The mRNA and protein expression were determined by immunohistochemistry, RT-PCR and western blot. Finally, hippocampus cells proliferation and apoptosis were examined by PCNA immunohistochemistry and TUNEL respectively.

resultsThe memory and learning was diminished in the propofol exposure group, however, the impaired memory and learning of rats were improved with the addition of NMDA and 7,8-DHF, while the improvement of memory and learning of rats were reversed with the addition of K252a and MK-801. In addition, the mRNA and protein expression levels and hippocampus cells proliferation were the same trend with the results of the MWM test, while apoptosis in hippocampus was reversed.

conclusionThe propofol can impair memory and learning of rats and induce cognition dysfunction through the interplay of NMDA receptor and BDNF-TrkB-CREB signaling pathway.

Indexed as

AnimalsBehavior, AnimalBlotting, WesternBrain-Derived Neurotrophic FactorCognitive DysfunctionDisease Models, AnimalHypnotics and SedativesIn Situ Nick-End LabelingMaze LearningMemoryPolymerase Chain ReactionPropofolRatsRats, Sprague-DawleyReceptors, N-Methyl-D-AspartateSignal TransductionBdnf protein, ratBrain-Derived Neurotrophic FactorHypnotics and SedativesPropofolReceptors, N-Methyl-D-AspartateBDNFCognition dysfunctionNMDAPropofolTrkB

Identifiers

PMID29621970
PMCPMC5887174
OpenAlexW2805094637

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.