Evidence map›Paper›PMID 42187503›Full record

ArticlePhysiological research2026

Synergistic Cardiac Protection by Thymoquinone and Valproic Acid in Absence Epilepsy.

Y A Cimen, F B Karakaya-Cimen, H Demirci, O T Cilingir-Kaya

Abstract read
In one paragraph

Article in Physiological research, 2026. 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

What it found

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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

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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.

Y A CimenDepartment of Physiology, Faculty of Medicine, Yalova University, Yalova, tugce.cilingir@marmara.edu.tr.
F B Karakaya-Cimen
H Demirci
O T Cilingir-Kaya

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to investigate the effects of thymoquinone (T) and valproic acid (VPA), alone and in combination, on cardiomyocyte damage induced by absence epilepsy (AE) in rats. Adult male Wistar rats (C, T) and Genetic Absence Epilepsy Rats from Strasbourg (GAERS; AE, AE+T, AE+V, AE+V+T) were assigned to six experimental groups. C and AE received solvent; T and AE+T received thymoquinone (10 mg/kg, o.g.); AE+V received VPA (200 mg/kg, i.p.); AE+V+T received both treatments for 8 days. Hearts were collected for histological (Masson's trichrome) and biochemical analyses. AE caused molecular changes in cardiomyocytes without fibrosis, decreasing total antioxidant status (TAS) (-8.7 %) and increasing total oxidant status (TOS) (+50.7 %), oxidative stress index (OSI) (+155.5 %), MDA (+50.8 %), caspase-8 (+43.8 %), cleaved caspase-3 (+73.5 %), NF-?B (+239.4 %), TNF-? (+141.2 %), IL-6 (+12.9 %). Compared with the AE group, T increased TAS (+48.2 %), IL-6 (+5.8 %) and reduced OSI (-36.7 %), caspase-8 (-16.0 %), cleaved caspase-3 (-37.5 %), TNF-? (-1.8 %). VPA increased TAS (+58.5 %), while reducing TOS (-15.7 %), OSI (-48.9 %), MDA (-31.9 %), IL-6 (-14.1 %), caspase-8 (-27.3 %), cleaved caspase-3 (-51.0 %), TNF-alpha (-8.9 %), and NF-kappaB (-28.5 %). The VPA+T combination further improved these alterations, decreasing TOS (-24.8 %), OSI (-54.5 %), MDA (-35.6 %), TNF-alpha (-16.3 %), caspase-8 (-27.7 %), cleaved caspase-3 (-47.1 %), NF-kappaB (-31.8 %) and IL-6 (-26.9 %) while increasing TAS (+59.8 %). Our study demonstrates that AE increases oxidative stress, apoptosis and inflammation in cardiac tissue. While T and VPA alone showed limited protective effects, their combined administration significantly attenuated cardiac damage, supporting this approach as a promising strategy for cardiac protection.

Indexed as

AnticonvulsantsBenzoquinonesCardiotonic AgentsEpilepsy, AbsenceMyocytes, CardiacValproic AcidAnimalsAntioxidantsDrug SynergismMaleOxidative StressRatsRats, WistarAnticonvulsantsAntioxidantsBenzoquinonesCardiotonic AgentsthymoquinoneValproic Acid

Identifiers

PMID42187503
PMCPMC13225446

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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.