Evidence map›Paper›PMID 40952476›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2026

Amelioration of intestinal ischemia reperfusion injury by diacerein via regulation of inflammasome/caspase-1/IL-1β and Wnt/β-catenin pathways in juvenile rats.

Marwa Monier Mahmoud Refaie, Nada Amgad Mohamed Abdel Majeed, Sayed Shehata, Asmaa A Muhammed, Salma M Hassan, Hoda S Sherkawy, Fatma F Ali, Mohamed Rabie Saad, Mousa Mohsen, Shereen Mohammed Mohammed Elsaghir and 2 more

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Article in Naunyn-Schmiedeberg's archives of pharmacology, 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

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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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

12 authors.

Marwa Monier Mahmoud RefaieDepartment of Medical Pharmacology, Faculty of Medicine, Minia University, 61511, Minia, Egypt.
Nada Amgad Mohamed Abdel MajeedDepartment of Histology and Cell Biology, Faculty of Medicine, Minia University, 61511, Minia, Egypt.
Sayed ShehataDepartment of Cardiology, Faculty of Medicine, Minia University, 61511, Minia, Egypt.
Asmaa A MuhammedDepartment of Medical Physiology, Faculty of Medicine, Aswan University, Aswan, 81528, Egypt. asmaa.ali@med.aswu.edu.eg.ORCID http://orcid.org/0000-0001-5998-9739
Salma M HassanDepartment of Human Anatomy and Embryology, Faculty of Medicine, Minia University, 61511, Minia, Egypt.
Hoda S SherkawyDepartment of Medical Biochemistry, Faculty of Medicine, Aswan University, Aswan, 81528, Egypt.
Fatma F AliDepartment of Medical Physiology, Faculty of Medicine, Minia University, 61511, Minia, Egypt.
Mohamed Rabie SaadDepartment of Surgery, Faculty of Medicine, Aswan University, Aswan, 81528, Egypt.
Mousa MohsenDepartment of Pediatrics, Faculty of Medicine, Aswan University, Aswan, 81528, Egypt.
Shereen Mohammed Mohammed ElsaghirDepartment of Internal Medicine, Faculty of Medicine, Minia University, Minia, 61511, Egypt.
Enas FathyDepartment of Cardiology, Faculty of Medicine, Aswan University, 81528, Aswan, Egypt.
Olivia N BeshayDepartment of Biochemistry, Faculty of Pharmacy, Minia University, 61511, Minia, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intestinal ischemia reperfusion (II/R) is an abdominal critical case especially in neonates and during childhood affecting not only the intestinal tissue but also it could damage other remote organs including cardiac tissue even following surgical intervention. Immune homeostasis during II/R has a major role in controlling its progression. Thus, finding additive medical treatment besides the surgical one becomes an urgent need to keep the tissue. So that, we aimed to evaluate the possible ameliorative effect of diacerein (DIA) on II/R-induced injury in juvenile rats. Forty juvenile rats of Wistar albino species were randomly allocated into four different groups: sham group, DIA given group, II/R group via clamping superior mesenteric artery, DIA-treated group (50 mg/kg) with induction of II/R. Data of current model revealed a significant elevation of the measured cardiac enzymes, cleaved caspase-3, and nuclear factor kappa β (NF-κB) in the untreated ischemic group with disturbed oxidative stress parameters, accompanied with dysregulation of inflammasome/caspase-1/IL-1β and Wnt/β-catenin signaling cascades. Fortunately, upon co-administration of DIA, there is a significant decrease of cardiac enzymes, cleaved caspase-3, and NF-κB with normalization of oxidative stress parameters and regulation of inflammasome/caspase-1/IL-1β and Wnt/β-catenin pathways confirmed by marked mitigation of the histopathological changes. This effect of DIA is greatly attributed to its pharmacological properties including IL-1β antagonist effect, anti-oxidant, anti-apoptotic, and anti-inflammatory properties. Thus, DIA could be considered as an adjuvant future medical therapy for those cases of II/R.

Indexed as

AnthraquinonesAnti-Inflammatory AgentsInflammasomesIntestinesReperfusion InjuryAnimalsCaspase 1Interleukin-1betaMaleOxidative StressRatsRats, WistarWnt Signaling PathwayAnthraquinonesAnti-Inflammatory AgentsCaspase 1diacereinIL1B protein, ratInflammasomesInterleukin-1betaDiacereinInflammasomeInterleukin-1βIntestinal ischemia reperfusion

Identifiers

PMID40952476
PMCPMC12901077

What Socratic holds

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LicenceCC BY
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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 Socratic graph.