Evidence map›Paper›PMID 37380907›Full record

ArticleActa neurochirurgica2023

Oxiracetam alleviates anti-inflammatory activity and ameliorates cognitive impairment in the early phase of traumatic brain injury.

Dong Hyuk Youn, Sung Woo Han, Jong-Tae Kim, Haesuk Choi, Aran Lee, Nayoung Kim, Harry Jung, Eun Pyo Hong, Chan Hum Park, Younghyurk Lee and 2 more

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In one paragraph

Article in Acta neurochirurgica, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
1.2field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 10 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

12 authors at 2 institutions in 1 country.

Dong Hyuk Youn *Institute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Sung Woo Han *Institute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Jong-Tae KimInstitute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Haesuk ChoiInstitute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Aran LeeInstitute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Nayoung KimInstitute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Harry JungInstitute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Eun Pyo HongInstitute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Chan Hum ParkInstitute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Younghyurk LeeInstitute of New Frontier Research, Hallym University College of Medicine, Chuncheon, Korea.
Sung Min ChoDepartment of Neurosurgery, Yonsei University Wonju College of Medicine, 20, Ilsan-RoGangwon-Do, Wonju, 26426, Korea. ns1287@hanmail.net.
Jin Pyeong JeonDepartment of Neurosurgery, Hallym University College of Medicine, 77 Sakju-Ro, Chuncheon, 24253, Korea. jjs6553@daum.net.ORCID http://orcid.org/0000-0001-8543-6855
Hallym University · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe aimed to investigate the effects of oxiracetam on cognitive impairment in the early phase of traumatic brain injury (TBI), for which no specific treatment is currently available.

methodsThe in vitro study used a cell injury controller to damage SH-SY5Y cells and evaluate the effect of oxiracetam at a dosage of 100 nM. The in vivo study used a stereotaxic impactor to induce a TBI model in C57BL/6 J mice and analyzed immunohistochemical changes and cognitive function after an intraperitoneal injection of oxiracetam (30 mg/kg/day) for 5 days. The number of mice used in this study was 60. They were divided into three groups (sham, TBI, and TBI with oxiracetam treatment) (20 mice in each group).

resultsThe in vitro study showed that oxiracetam treatment resulted in increased superoxide dismutase (SOD)1 and SOD2 mRNA expression. The mRNA and protein expression of COX-2, NLRP3, caspase-1, and interleukin (IL)-1 β were decreased after oxiracetam treatment, along with decreases in intracellular reactive oxygen species production and apoptotic effects. TBI mice treated with oxiracetam exhibited the loss of fewer cortical damaged lesions, less brain edema, and fewer Fluoro-Jade B (FJB)-positive and terminal deoxynucleotidyl transferase dUTP nick end-labeling (TUNEL)-positive cells compared to those without oxiracetam treatment. The mRNA and protein expression of COX-2, NLRP3, caspase-1, and IL-1β were decreased significantly after oxiracetam treatment. These inflammation-related markers, which colocalized with Iba-1-positive or GFAP-positive cells after TBI, were also decreased after oxiracetam treatment. TBI mice treated with oxiracetam had a smaller decrease in preference and more latency time than those not treated with oxiracetam, suggesting the amelioration of impaired cognitive impairment.

conclusionsOxiracetam may be helpful in restoring cognitive impairment by ameliorating neuroinflammation in the early phase of TBI.

Indexed as

Brain Injuries, TraumaticCognitive DysfunctionNeuroblastomaAnimalsAnti-Inflammatory AgentsCaspasesCyclooxygenase 2Disease Models, AnimalHumansMiceMice, Inbred C57BLNLR Family, Pyrin Domain-Containing 3 ProteinPyrrolidinesRatsRats, Sprague-DawleyRNA, MessengerAnti-Inflammatory AgentsCaspasesCyclooxygenase 2NLR Family, Pyrin Domain-Containing 3 ProteinoxiracetamPyrrolidinesRNA, MessengerCognitionNeuroinflammationOxiracetamTraumatic brain injury

Identifiers

PMID37380907
OpenAlexW4382361893

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.