Evidence map›Paper›PMID 42018894›Full record

ArticleActa cirurgica brasileira2026

Thymoquinone and caffeic acid phenethyl ester mitigate experimental ulcerative colitis: a biochemical and histopathological study.

Can Ersak, Ender Ergüder, Jafar Nouri Nojadeh, Saygin Altiner, Mevlut Recep Pekcici

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Article in Acta cirurgica brasileira, 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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1 · What the graph read from it

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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

5 authors.

Can ErsakHealth Sciences University - Ankara Training and Research Hospital - General Surgery - Ankara - Turkey.ORCID http://orcid.org/0000-0002-9658-6063
Ender ErgüderHealth Sciences University - Etlik City Hospital - General Surgery Department - Ankara - Turkey.ORCID http://orcid.org/0000-0001-5289-3718
Jafar Nouri NojadehAnkara University - Faculty of Medicine - Department of Medical Biochemistry - Ankara - Turkey.ORCID http://orcid.org/0000-0002-2468-2996
Saygin AltinerGazi University - Faculty of Medicine - Department of General Surgery - Ankara - Turkey.ORCID http://orcid.org/0000-0001-6118-9984
Mevlut Recep PekciciHealth Sciences University - Ankara Training and Research Hospital - General Surgery - Ankara - Turkey.ORCID http://orcid.org/0000-0002-5566-8134

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo establish an acetic acid-induced acute ulcerative colitis model in rats and to evaluate the clinical, biochemical, and histopathological effects of thymoquinone (TQ) and caffeic acid phenethyl ester (CAPE) in this model.

methodsForty male Wistar albino rats (190-303 g) were randomly assigned to five groups (n = 8). All groups except the control received rectal acetic acid (4%) to induce colitis. Group 1 (control) received intraperitoneally (IP) 0.9% saline for five days. Group 2 (colitis) received IP 10% ethanol (vehicle for CAPE). Group 3 (TQ) received IP thymoquinone (10 mg/kg/day). Group 4 (CAPE) received IP caffeic acid phenethyl ester (10 µmol/kg/day). Group 5 (TQ+CAPE) received both agents at the same doses. On day 5, animals were euthanized, and colon and serum samples were collected for biochemical and histopathological analysis.

resultsSignificant differences were observed in the disease activity index, tumor necrosis factor-α, catalase, glutathione peroxidase, interleukin-10, and malondialdehyte indicating a balance between oxidant and antioxidant parameters. CAPE was found to have a greater anti-inflammatory effect than TQ histopathologically. The combined administration of CAPE and TQ mitigated oxidative stress as demonstrated by decreased oxidative stress biomarkers and improved antioxidant protection.

conclusionBoth CAPE and TQ demonstrated anti-inflammatory and antioxidant effects in an acetic acid-induced colitis model, with CAPE showing greater histological improvement. Their combined administration yielded additional benefits in oxidative stress reduction. These findings suggest that CAPE and TQ, particularly in combination, may hold promise as adjunctive agents in colitis management and warrant further investigation.

Indexed as

AntioxidantsBenzoquinonesCaffeic AcidsColitis, UlcerativePhenylethyl AlcoholAcetic AcidAnimalsCatalaseColonDisease Models, AnimalGlutathione PeroxidaseInterleukin-10MaleMalondialdehydeOxidative StressRandom AllocationAcetic AcidAntioxidantsBenzoquinonescaffeic acid phenethyl esterCaffeic AcidsCatalaseGlutathione PeroxidaseInterleukin-10MalondialdehydePhenylethyl AlcoholthymoquinoneTumor Necrosis Factor-alpha

Identifiers

PMID42018894
PMCPMC13120787

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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.