Evidence map›Paper›PMID 31721903›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica2019

Oxiracetam ameliorates cognitive deficits in vascular dementia rats by regulating the expression of neuronal apoptosis/autophagy-related genes associated with the activation of the Akt/mTOR signaling pathway.

Jing Xu, Qianqian Qi, Peiyuan Lv, Yanhong Dong, Xin Jiang, Zhijuan Liu

Open access · goldAbstract read
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 38 citations in OpenAlex.

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  12. Marinoid J, a phenylglycoside fromPharmaceutical biology · 2020
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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

6 authors at 1 institution in 1 country.

Jing XuDepartment of Neurology, Hebei General Hospital, Shijiazhuang City, Hebei Province, China.ORCID http://orcid.org/0000-0001-9435-7729
Qianqian QiDepartment of Neurology, Hebei General Hospital, Shijiazhuang City, Hebei Province, China.ORCID http://orcid.org/0000-0003-3303-1973
Peiyuan LvDepartment of Neurology, Hebei General Hospital, Shijiazhuang City, Hebei Province, China.ORCID http://orcid.org/0000-0002-8871-5224
Yanhong DongDepartment of Neurology, Hebei General Hospital, Shijiazhuang City, Hebei Province, China.ORCID http://orcid.org/0000-0003-2505-8172
Xin JiangDepartment of Neurology, Hebei General Hospital, Shijiazhuang City, Hebei Province, China.ORCID http://orcid.org/0000-0001-6663-4063
Zhijuan LiuDepartment of Neurology, Hebei General Hospital, Shijiazhuang City, Hebei Province, China.ORCID http://orcid.org/0000-0002-5777-8839
Hebei General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxiracetam (ORC) is a commonly used nootropic drug for improving cognition and memory impairments. The therapeutic effect and underlying mechanism of ORC in vascular dementia (VaD) treatment remain unknown. In this study, 3-month-old male Sprague-Dawley rats with permanent bilateral common carotid artery occlusion-induced VaD were treated orally with low (100 mg/kg) or high (200 mg/kg) dose ORC once a day for 4 weeks. The results of the Morris water maze test and Nissl staining showed that ORC treatment significantly alleviated learning and memory deficits and neuronal damage in rats with VaD. Mechanistically, the protein levels of a panel of genes associated with neuronal apoptosis (Bcl-2, Bax) and autophagy (microtubule-associated protein 1 chain 3, Beclin1, p62) were significantly altered by ORC treatment compared with VaD, suggesting a protective role of ORC against VaD-induced neuronal apoptosis and autophagy. Moreover, the Akt/mTOR pathway, which is known to be the upstream signaling governing apoptosis and autophagy, was found to be activated in ORC-treated rats, suggesting an involvement of Akt/mTOR activation in ORC-rendered protection in VaD rats. Taken together, this study demonstrated that ORC may alleviate learning and memory impairments and neuronal damage in VaD rats by altering the expression of apoptosis/autophagy-related genes and activation of the Akt/mTOR signaling pathway in neurons.

Indexed as

AnimalsApoptosisAutophagyCognitive DysfunctionDementia, VascularDisease Models, AnimalMaleMaze LearningNeuroprotective AgentsProto-Oncogene Proteins c-aktPyrrolidinesRatsRats, Sprague-DawleySignal TransductionTOR Serine-Threonine KinasesmTOR protein, ratNeuroprotective AgentsoxiracetamProto-Oncogene Proteins c-aktPyrrolidinesTOR Serine-Threonine Kinases

Identifiers

PMID31721903
PMCPMC6853072
OpenAlexW2988695884

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.