Evidence map›Paper›PMID 41221903›Full record

ArticleActa cirurgica brasileira2025

Dose-dependent protective profile of trans-anethole in experimental traumatic brain injury in mice via modulation of apoptotic and inflammatory protein expression, and oxidative stress.

Aziz Çevik, Burak Atlas, Gamze Erdoğan, Mehmet Salih Atama, Barış Altun, Tevfik Yılmaz

Abstract read
In one paragraph

Article in Acta cirurgica brasileira, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Aziz ÇevikDicle University - Faculty of Medicine - Department of Neurosurgery - Diyarbakır - Turkey.ORCID http://orcid.org/0009-0009-9804-3992
Burak AtlasDicle University - Faculty of Medicine - Department of Neurosurgery - Diyarbakır - Turkey.ORCID http://orcid.org/0000-0002-4895-0916
Gamze ErdoğanDicle University - Faculty of Medicine - Department of Histology and Embryology - Diyarbakır - Turkey.ORCID http://orcid.org/0000-0002-5854-8517
Mehmet Salih AtamaGenesis Private Hospital - Department of Neurosurgery - Diyarbakır - Turkey.ORCID http://orcid.org/0009-0009-6445-876X
Barış AltunNusaybin State Hospital - Department of Neurosurgery - Nusaybin - Mardin - Turkey.ORCID http://orcid.org/0000-0002-2727-1025
Tevfik YılmazDicle University - Faculty of Medicine - Department of Neurosurgery - Diyarbakır - Turkey.ORCID http://orcid.org/0000-0002-1444-3246

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo investigate the protective effect of trans-anethole in experimental traumatic brain injury (TBI) in mice.

methodsThirty-five adult mice were divided into five groups (control, TBI, TBI+A40, TBI+A80, and TBI+A160). No treatment was performed in the control group. The treated groups (TBI+A40, TBI+A80, and TBI+A160) received 40, 80 or 160 mg/kg trans-anethole treatment, respectively. At the end of the experiment, the brains of the sacrificed animals were removed, and laboratory analyses were performed.

resultsMalondialdehyde (MDA) levels in brain tissue of TBI and TBI+A40 were significantly increased, while MDA levels of TBI+A80 and TBI were similar. TBI+A160 and control tissue MDA levels were similar (p > 0.05), significantly different from TBI (p < 0.01). Immunodensity analyses showed that there was a significant difference between the control and TBI in terms of Bax, caspase 3, tumor necrosis factor-α (TNF-α) and interleukin- (IL)-1β immunoexpression. TBI+A40 immunoexpression was similar to TBI (p > 0.05), significantly different from the control groups (p < 0.05). In TBI+A80 and TBI+A160, pro-apoptotic Bax and caspase 3, pro-inflammatory TNF-α and IL-1β levels were also significantly improved. Immunoexpression levels of TBI+A160 and control were similar (p > 0.05).

conclusionin our study, trans-anethole treatment had a dose-dependent neuroprotective potential against trauma-induced neurodegeneration.

Indexed as

AnisolesApoptosisBrain Injuries, TraumaticNeuroprotective AgentsOxidative StressAllylbenzene DerivativesAnimalsCaspase 3Disease Models, AnimalDose-Response Relationship, DrugInterleukin-1betaMaleMalondialdehydeMiceTumor Necrosis Factor-alphaAllylbenzene DerivativesanetholeAnisolesCaspase 3Interleukin-1betaMalondialdehydeNeuroprotective AgentsTumor Necrosis Factor-alpha

Identifiers

PMID41221903
PMCPMC12600009

What Socratic holds

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LicenceCC BY
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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 Socratic graph.