Evidence map›Paper›PMID 30081596›Full record

ArticleInternational journal of molecular sciences2018

AAV-Syn-BDNF-EGFP Virus Construct Exerts Neuroprotective Action on the Hippocampal Neural Network during Hypoxia In Vitro.

Еlena V Mitroshina, Tatiana A Mishchenko, Alexandra V Usenko, Ekaterina A Epifanova, Roman S Yarkov, Maria S Gavrish, Alexey A Babaev, Maria V Vedunova

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 22 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 2 institutions in 1 country.

Еlena V MitroshinaLobachevsky State University of Nizhni Novgorod, Institute of Neuroscience, 23 Prospekt Gagarina, 603950 Nizhny Novgorod, Russia. helenmitroshina@gmail.com.
Tatiana A MishchenkoLobachevsky State University of Nizhni Novgorod, Institute of Neuroscience, 23 Prospekt Gagarina, 603950 Nizhny Novgorod, Russia. saHarnova87@mail.ru.
Alexandra V UsenkoLobachevsky State University of Nizhni Novgorod, Institute of Neuroscience, 23 Prospekt Gagarina, 603950 Nizhny Novgorod, Russia. sas7342415@mail.ru.
Ekaterina A EpifanovaLobachevsky State University of Nizhni Novgorod, Institute of Neuroscience, 23 Prospekt Gagarina, 603950 Nizhny Novgorod, Russia. epifa888@mail.ru.
Roman S YarkovLobachevsky State University of Nizhni Novgorod, Institute of Neuroscience, 23 Prospekt Gagarina, 603950 Nizhny Novgorod, Russia. roman.sultanov.96@mail.ru.
Maria S GavrishLobachevsky State University of Nizhni Novgorod, Institute of Neuroscience, 23 Prospekt Gagarina, 603950 Nizhny Novgorod, Russia. gavrish@neuro.nnov.ru.
Alexey A BabaevLobachevsky State University of Nizhni Novgorod, Institute of Neuroscience, 23 Prospekt Gagarina, 603950 Nizhny Novgorod, Russia. alexisbabaev@list.ru.
Maria V VedunovaLobachevsky State University of Nizhni Novgorod, Institute of Neuroscience, 23 Prospekt Gagarina, 603950 Nizhny Novgorod, Russia. MVedunova@yandex.ru.
N. I. Lobachevsky State University of Nizhny Novgorod · RUPrivolzhsky Research Medical University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain-derived neurotrophic factor (BDNF) is one of the key signaling molecules that supports the viability of neural cells in various brain pathologies, and can be considered a potential therapeutic agent. However, several methodological difficulties, such as overcoming the blood⁻brain barrier and the short half-life period, challenge the potential use of BDNF in clinical practice. Gene therapy could overcome these limitations. Investigating the influence of viral vectors on the neural network level is of particular interest because viral overexpression affects different aspects of cell metabolism and interactions between neurons. The present work aimed to investigate the influence of the adeno-associated virus (AAV)-Syn-BDNF-EGFP virus construct on neural network activity parameters in an acute hypobaric hypoxia model in vitro. MATERIALS AND

methodsAn adeno-associated virus vector carrying the

resultsBDNF overexpression by AAV-Syn-BDNF-EGFP does not affect cell viability or the main parameters of spontaneous bioelectrical activity in normoxia. Application of the developed virus construct partially eliminates the negative hypoxic consequences by preserving cell viability and maintaining spontaneous bioelectrical activity in the cultures. Moreover, the internal functional structure, including the activation pattern of network bursts, the number of hubs, and the number of connections within network elements, is also partially preserved. BDNF overexpression prevents a decrease in the number of cells exhibiting calcium activity and maintains the frequency of calcium oscillations.

conclusionThis study revealed the pronounced antihypoxic and neuroprotective effects of AAV-Syn-BDNF-EGFP virus transduction in an acute normobaric hypoxia model.

Indexed as

AnimalsBrain-Derived Neurotrophic FactorCells, CulturedDependovirusGreen Fluorescent ProteinsHippocampusHypoxiaHypoxia, BrainMiceMice, Inbred C57BLNeuroprotectionBrain-Derived Neurotrophic Factorenhanced green fluorescent proteinGreen Fluorescent Proteinsadeno-associated virus vectorBDNFbrain-derived neurotrophic factorcalcium imagingcerebral hypoxiamultielectrode arraysneuroprotectionprimary hippocampal cell cultures

Identifiers

PMID30081596
PMCPMC6121472
OpenAlexW2885248803

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.