Evidence map›Paper›PMID 38468526›Full record

ArticleCurrent neurovascular research2024

Increased Cyclic Adenosine Monophosphate Responsive Element is Closely Associated with the Pathogenesis of Drug-resistant Epilepsy.

Jing-Xuan Li, Dai Shi, Si-Ying Ren, Guo-Feng Wu

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Article in Current neurovascular research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

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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

4 authors.

Jing-Xuan LiClinical College of Guizhou, Medical University, Guiyang, Guizhou, 561113, China.ORCID 0000-0002-2586-7861
Dai ShiSchool of Clinical Medicine, Guizhou Medical University, Guiyang, Guizhou, 561113, China.
Si-Ying RenClinical College of Guizhou, Medical University, Guiyang, Guizhou, 561113, China.
Guo-Feng WuClinical College of Guizhou, Medical University, Guiyang, Guizhou, 561113, China.

Funding

Guizhou Medical University (grant number gyfynsfc-2021-8).
6 · The paper itself

Abstract

backgroundDrug-resistant epilepsy (DRE) is a refractory neurological disorder. There is ample evidence that suggest that γ-aminobutyric acid-a (GABAA) receptors could be one of the mechanisms responsible for the development of drug resistance in epilepsy. It is also known that the cAMP response element binding protein (CREB) plays a possible key role in the transcriptional regulation of GABA

objectiveThis study explores the role of CREB in the development of DRE and the effect of CREB on GABA-related receptors in DRE.

methodsThe CREB expression was increased or decreased in the hippocampus of normal rats by lentiviral transfection, who then underwent the lithium-pilocarpine-induced epilepsy model. Phenobarbital (PB) sodium and carbamazepine (CBZ) were used to select a drug-resistant epileptic model. The expression levels of GABA

resultsThe frequency and duration of seizures increased in the overexpression group compared to that in the control group. In addition, the severity, frequency, and duration of seizures decreased in the group with decreased expression. The hippocampus analysis of the expression levels of the CREB protein and CREB mRNA yielded similar findings. Altering the CREB protein expression in the rat hippocampus could negatively regulate the expression and transcript levels of GABA

conclusionOur study shows that enhanced CREB expression promotes the development of DRE and negatively regulates GABA

Indexed as

Cyclic AMP Response Element-Binding ProteinDrug Resistant EpilepsyHippocampusRats, Sprague-DawleyReceptors, GABA-AAnimalsAnticonvulsantsDisease Models, AnimalMalePhenobarbitalPilocarpineRatsAnticonvulsantsCyclic AMP Response Element-Binding ProteinPhenobarbitalPilocarpineReceptors, GABA-ACREBdrug-resistant epilepsyEpilepsyGABA A receptorstatus epilepticus.γ-aminobutyric

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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.