Evidence map›Paper›PMID 33132901›Full record

ArticleFrontiers in aging neuroscience2020

GLT-1 Knockdown Inhibits Ceftriaxone-Mediated Improvements on Cognitive Deficits, and GLT-1 and xCT Expression and Activity in APP/PS1 AD Mice.

JunXia Gao, LiZhe Liu, Chao Liu, ShuJuan Fan, LiRong Liu, ShuFeng Liu, Xiao-Hui Xian, Wen-Bin Li

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2020. 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
0.9field-weighted citation impact, top 30% 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, 24 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

8 authors at 1 institution in 1 country.

JunXia GaoDepartment of Pathophysiology, Neuroscience Research Center, Hebei Medical University, Shijiazhuang, China.
LiZhe LiuDepartment of Pathophysiology, Neuroscience Research Center, Hebei Medical University, Shijiazhuang, China.
Chao LiuHebei Key Lab of Laboratory Animal Science, Laboratory Animal Center, Hebei Medical University, Shijiazhuang, China.
ShuJuan FanDepartment of Pathophysiology, Neuroscience Research Center, Hebei Medical University, Shijiazhuang, China.
LiRong LiuDepartment of Pathophysiology, Neuroscience Research Center, Hebei Medical University, Shijiazhuang, China.
ShuFeng LiuHebei Key Lab of Laboratory Animal Science, Laboratory Animal Center, Hebei Medical University, Shijiazhuang, China.
Xiao-Hui XianDepartment of Pathophysiology, Neuroscience Research Center, Hebei Medical University, Shijiazhuang, China.
Wen-Bin LiDepartment of Pathophysiology, Neuroscience Research Center, Hebei Medical University, Shijiazhuang, China.
Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveGlutamate transporter-1 (GLT-1) and system x

methodsGLT-1 knockdown (GLT-1

resultsIn comparison with wild-type mice, APP/PS1 mice exhibited significant cognitive deficits, represented with poor performance in novel object recognition and Morris water maze tests, downregulated GLT-1 expression and glutamate uptake. Ceftriaxone treatment significantly improved the above impairments in APP/PS1 mice, but had negligible impact in GLT-1

conclusionCeftriaxone improves cognitive impairment of APP/PS1 mice by upregulating GLT-1-mediated uptake of glutamate and co-regulation of GLT-1 and xCT in APP/PS1 mice.

Indexed as

APP/PS1 miceceftriaxoneGLT-1GLT-1 knockdownglutamate uptakeglutathione levelxCT

Identifiers

PMID33132901
PMCPMC7574737
OpenAlexW3092280597

What OpenQuestion holds

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LicenceCC BY
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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.