Evidence map›Paper›PMID 39316354›Full record

ArticleMolecular neurobiology2025

The Interactions of Resveratrol and Sodium Valproate on Penicillin-Induced Epilepsy Model: Electrophysiological and Molecular Study.

Zeynep Kasap Acungil, Secil Erden Tayhan, Nazan Goksen Tosun, Tuncer Nacar

Abstract read
PubMed Publisher
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Zeynep Kasap AcungilDepartment of Physiotherapy and Rehabilitation, Faculty of Health Science, Tokat Gaziosmanpasa University, Tokat, Turkey. zeynep.kasap@gop.edu.tr.ORCID http://orcid.org/0000-0003-0475-7628
Secil Erden TayhanDepartment of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tokat Gaziosmanpasa University, Tokat, Turkey.ORCID http://orcid.org/0000-0001-8473-5896
Nazan Goksen TosunDepartment of Medical Services and Techniques, Vocational School of Health Services, Tokat Gaziosmanpasa University, Tokat, Turkey.ORCID http://orcid.org/0000-0001-5269-1067
Tuncer NacarDepartment of Physiology, Faculty of Medicine, Yüksek Ihtisas University, Ankara, Turkey.ORCID http://orcid.org/0000-0002-9287-7170

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epilepsy represents the most prevalent chronic neurological disease, characterized by spontaneous recurrent seizures. In experimental epilepsy models created by different methods, resveratrol has been demonstrated to reduce epileptiform activity and exhibit neuroprotective properties. A penicillin-induced model of epileptogenesis was used to investigate the effects of resveratrol and its combination with sodium valproate on epileptiform activity. The study design was an in vivo animal experimental study. Forty Wistar-albino rats were divided into five groups, each with eight rats. The groups are categorized as the saline group, penicillin group (only penicillin), resveratrol group, sodium valproate group, and resveratrol + sodium valproate group. ECoG recording was taken for 180 min in all groups and statistically evaluated. GABAα1, mGluR1/mGluR5, NMDAR1 receptor expressions in the hippocampus, and S100B level in serum were measured. The spike frequency decreased statistically to 60th min in the sodium valproate group and 150th min in the resveratrol group. The spike frequency decreased statistically in the 20th min and later measurements of the recording in the resveratrol + sodium valproate group. GABAα1 receptor expression was increased in all groups compared to the penicillin group. mGluR1/mGluR5, NMDAR1 receptor expression was decreased in all groups compared to the penicillin group. Serum S100B level increased in all groups compared to the penicillin group. There was no statistically significant difference in epileptiform activity when resveratrol alone was administered in the penicillin-induced epilepsy model. Resveratrol co-administered with sodium valproate significantly reduced epileptiform activity. Co-administration of the sodium valproate + resveratrol group made the receptor level's highest GABAα1receptor expression at receptors.

Indexed as

EpilepsyPenicillinsResveratrolValproic AcidAnimalsDisease Models, AnimalDrug InteractionsHippocampusMaleRatsRats, WistarReceptor, Metabotropic Glutamate 5Receptors, GABA-AReceptors, Metabotropic GlutamateReceptors, N-Methyl-D-AspartateS100 Calcium Binding Protein beta Subunitmetabotropic glutamate receptor type 1PenicillinsReceptor, Metabotropic Glutamate 5Receptors, GABA-AReceptors, Metabotropic GlutamateReceptors, N-Methyl-D-AspartateResveratrolS100 Calcium Binding Protein beta SubunitValproic AcidGABAGlutamatePenicillin epilepsy modelResveratrolS100B

Identifiers

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.