Evidence map›Paper›PMID 41934501›Full record

ArticleJournal of molecular histology2026

The anti-ulcerative potential of Berberine on the rat model of inflammatory bowel disease.

Ghadha Ibrahim Fouad, Hanan F Aly, Dalia A Taha, Karima A Hamed, Ayda K Kelany, Wagdy K B Khalil, Maha Z Rizk

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Article in Journal of molecular histology, 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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0cells of the map it votes in
0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

7 authors.

Ghadha Ibrahim FouadDepartment of Therapeutic Chemistry, Pharmaceutical and Drug Industries Research Institute, National Research Centre, 33 El Bohouth St., PO Box 12622, Dokki, Cairo, Egypt. ghadhaibrahim@yahoo.com.ORCID http://orcid.org/0000-0003-3665-3153
Hanan F AlyDepartment of Therapeutic Chemistry, Pharmaceutical and Drug Industries Research Institute, National Research Centre, 33 El Bohouth St., PO Box 12622, Dokki, Cairo, Egypt.
Dalia A TahaDepartment of Cell Biology, National Research Centre, El-Bohouth St., 12262, Cairo, Egypt.
Karima A HamedDepartment of Cell Biology, National Research Centre, El-Bohouth St., 12262, Cairo, Egypt.
Ayda K KelanyDepartment of Genomic Medicine, Cairo University Hospitals, Cairo University, Giza, Cairo, Egypt.
Wagdy K B KhalilDepartment of Cell Biology, National Research Centre, El-Bohouth St., 12262, Cairo, Egypt.
Maha Z RizkDepartment of Therapeutic Chemistry, Pharmaceutical and Drug Industries Research Institute, National Research Centre, 33 El Bohouth St., PO Box 12622, Dokki, Cairo, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ulcerative colitis (UC) is a global inflammatory bowel disease (IBD) and is a chronic mucosal inflammation of the large intestine. UC is accompanied by the increment in the production and release of pro-inflammatory mediators. Due to the immunomodulatory potentials of Berberine (BBN), the present study aimed at examining its anti-ulcerogenic activity against experimentally induced ulcerative colitis (UC), by intrarectal instillation of 1 ml of 3% acetic acid (AA). Thirty adults female Wistar rats were divided into three groups: (1) Negative control, (2) AA-induced UC rats (intrarectal), (3) Treated AA-induced UC + BBN (50 mg/kg/day; orally). Biochemical, molecular, histopathological, and immunohistochemical investigations were conducted. Intrarectal administration of AA provoked several macroscopic and microscopic alterations in the colons of UC-induced rats, increased the colonic lipid peroxidation, upregulated the expression of nuclear factor kappa B (NF-κB), caspase-3, and interferon gamma (IFN-γ), increased levels of colonic inflammatory tumor necrosis factor-alpha (TNF-α), Interleukin-1 beta (IL-1β), and prostaglandin E 2 (PGE-2), and downregulated the immunoexpression of nuclear factor erythroid 2-related factor 2 (Nrf-2). In contrast, treatment of UC-rats with BBN exhibited curative activities manifested by downregulating the expression of NF-κB and caspase-3, reducing the colonic contents of malondialdehyde (MDA), TNF-α, IL-1β, and PGE-2; and activating Nrf-2 immunoexpression. This study evidenced the anti-ulcerative and colo-therapeutic potentials of BBN that might be ascribed to its anti-lipid peroxidation, anti-apoptotic, and anti-inflammatory activities.

Indexed as

BerberineColitis, UlcerativeInflammatory Bowel DiseasesAcetic AcidAnimalsCaspase 3ColonDisease Models, AnimalFemaleLipid PeroxidationNF-kappa BRatsRats, WistarAcetic AcidBerberineCaspase 3NF-kappa BAcetic acidBerberineInflammatory bowel diseaseMalondialdehydeNrf-2Prostaglandin E2Ulcerative colitis

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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.