Evidence map›Paper›PMID 39514020›Full record

ArticleCell and tissue research2025

The possible protective effect of luteolin on cardiovascular and hepatic changes in metabolic syndrome rat model.

Heba Fikry, Lobna A Saleh, Doaa Ramadan Sadek, Hadwa Ali Abd Alkhalek

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Article in Cell and tissue research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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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

4 authors.

Heba FikryDepartment of Histology and Cell Biology, Faculty of Medicine, Ain Shams University, Khalifa El-Maamon St, Abbasiya Sq., Cairo, Egypt. hebafikry@med.asu.edu.eg.ORCID http://orcid.org/0000-0002-0046-9875
Lobna A SalehDepartment of Clinical Pharmacology, Faculty of Medicine, Ain Shams University, Khalifa El-Maamon St, Abbasiya Sq., Cairo, Egypt.ORCID http://orcid.org/0000-0003-0949-9429
Doaa Ramadan SadekDepartment of Histology and Cell Biology, Faculty of Medicine, Ain Shams University, Khalifa El-Maamon St, Abbasiya Sq., Cairo, Egypt.
Hadwa Ali Abd AlkhalekDepartment of Histology and Cell Biology, Faculty of Medicine, Ain Shams University, Khalifa El-Maamon St, Abbasiya Sq., Cairo, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The metabolic syndrome, or MetS, is currently a global health concern. The anti-inflammatory, anti-proliferative, and antioxidant properties of luteolin are some of its advantageous pharmacological characteristics. This research was designed to establish a MetS rat model and investigate the possible protective effect of luteolin on cardiovascular, hepatic, and metabolic changes in diet-induced metabolic syndrome in rats. Forty adult male albino rats were split into four groups: a negative control group, a group treated with luteolin, a group induced MetS (fed 20% fructose), and a group treated with luteolin (fed 20% fructose and given luteolin). Following the experiment after 8 weeks, biochemical, histological (light and electron), and immunohistochemistry analyses were performed on liver and heart tissues. Serum levels of cTnI, CK-MB, and LDH were significantly elevated in response to the cardiovascular effect of MetS. Furthermore, compared to the negative control group, the MetS group showed a marked increase in lipid peroxidation in the cardiac and hepatic tissues, as evidenced by elevated levels of MDA and a decline in the antioxidant defense system, as demonstrated by lower activities of GSH and SOD. The fatty liver-induced group exhibited histological alterations, including disrupted hepatic architecture, dilated and congested central veins, blood sinusoids, and portal veins. In addition to nuclear structural alterations, most hepatocytes displayed varying degrees of cytoplasmic vacuolation, mitochondrial alterations, and endoplasmic reticulum dilatation. These alterations were linked to inflammatory cellular infiltrations, collagen fiber deposition, active hepatic stellate cells, and scattered hypertrophied Kupffer cells, as demonstrated by electron microscopy and validated by immunohistochemical analysis. It is interesting to note that eosinophils were seen between the liver cells and in dilated blood sinusoids. Moreover, the biochemical (hepatic and cardiac) and histological (liver) changes were significantly less severe in luteolin-treated rat on a high-fructose diet. These results suggested that luteolin protects against a type of metabolic syndrome that is produced experimentally.

Indexed as

Cardiovascular SystemLiverLuteolinMetabolic SyndromeProtective AgentsAnimalsAntioxidantsDisease Models, AnimalFructoseLipid PeroxidationMaleMyocardiumRatsAntioxidantsFructoseLuteolinProtective AgentsFructoseHeartHistologicalLiverMetabolic syndromeRats

Identifiers

PMID39514020

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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.