Evidence map›Paper›PMID 42884083›Full record

ArticleInternational journal of molecular sciences2026

Cynaroside Attenuates Ethinylestradiol-Induced Cholestatic Liver Injury by Modulating the FXR/BSEP/CYP7A1/SHP Axis.

Amany M Hamed, Doha M Al-Nouri, Nadia S Mahrous, Asmaa Sabry Bassit, Azza M A Abouelella, Asmaa Hassan, Gehad S Mokhtar, Ghada M Ahmad, Ahmed S Osman, Ahmed R H Ahmed and 7 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

17 authors.

Amany M HamedChemistry Department, Faculty of Science, Sohag University, Sohag 82524, Egypt.ORCID 0000-0002-5995-8358
Doha M Al-NouriDepartment of Food and Nutrition Sciences, College of Food and Agriculture Sciences, King Saud University, Riyadh 11495, Saudi Arabia.ORCID 0000-0002-1230-1471
Nadia S MahrousDepartment of Zoology, Faculty of Science, South Valley University, Qena 83523, Egypt.
Asmaa Sabry BassitAnatomy & Embryology Department, Faculty of Medicine, Sohag University, Sohag 82524, Egypt.
Azza M A AbouelellaDepartment of Clinical Pharmacology, Faculty of Medicine, Sohag University, Sohag 82524, Egypt.
Asmaa HassanDepartment of Physiology, Faculty of Medicine, Sohag University, Sohag 82524, Egypt.
Gehad S MokhtarDepartment of Molecular Biology, Faculty of Applied Biotechnology, Merit University, Sohag 82755, Egypt.
Ghada M AhmadDepartment of Medical Laboratory Technology, Faculty of Applied Health Sciences Technology, Pharos University in Alexandria, Canal El Mahmoudia Street, Beside Green Plaza Complex, Alexandria 21648, Egypt.ORCID 0000-0002-6824-5683
Ahmed S OsmanDepartment of Biochemistry, Faculty of Veterinary Medicine, Sohag University, Sohag 82524, Egypt.
Ahmed R H AhmedDepartment of Pathology, Faculty of Medicine, Sohag University, Sohag 82524, Egypt.ORCID 0000-0003-2923-7012
Aya A E MahgoobTechnology of Medical Laboratory Department, Higher Technology Institute of Applied Health Sciences, Badr Academy for Technology and Sciences, Badr City 11829, Egypt.
Shymaa A ThabetCentral Research Center, Faculty of Medicine, Sohag University, Sohag 82524, Egypt.
Hany M R Abdel-LatifDepartment of Poultry and Fish Diseases, Faculty of Veterinary Medicine, Alexandria University, Alexandria 26571, Egypt.ORCID 0000-0001-8761-1493
Ghalia ShamlanDepartment of Food and Nutrition Sciences, College of Food and Agriculture Sciences, King Saud University, Riyadh 11495, Saudi Arabia.ORCID 0000-0002-3095-3430
Haifeng ZhaoSchool of Food Science and Engineering, South China University of Technology, Guangzhou 510640, China.ORCID 0000-0001-6009-3526
Ammar Al-FargaDepartment of Biological Sciences, College of Science, University of Jeddah, Jeddah 21589, Saudi Arabia.ORCID 0000-0002-0233-5539
Safaa S SolimanDepartment of Zoology, Faculty of Science, Minia University, Minia 61519, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholestatic liver diseases are characterized by disrupted bile acid homeostasis, oxidative stress, and inflammation, ultimately leading to progressive hepatic injury. Although ursodeoxycholic acid (UDCA) remains the standard pharmacological therapy, its therapeutic efficacy is limited in several cholestatic conditions. This study investigated the hepatoprotective effects of cynaroside (CYN), a naturally occurring flavonoid glycoside, against ethinylestradiol (EE)-induced cholestatic liver injury and explored its underlying molecular mechanisms. Female Wistar rats were randomly allocated into four groups (

Indexed as

Chemical and Drug Induced Liver InjuryCholestasisCholesterol 7-alpha-HydroxylaseEthinyl EstradiolLuteolinReceptors, Cytoplasmic and NuclearAnimalsATP Binding Cassette Transporter, Subfamily B, Member 11FemaleLiverMolecular Docking SimulationOxidative StressRatsRats, WistarReceptor, Farnesoid X-ActivatedSignal TransductionAbcb11 protein, ratATP Binding Cassette Transporter, Subfamily B, Member 11Cholesterol 7-alpha-HydroxylaseCYP7A1 protein, ratEthinyl EstradiolLuteolinnuclear receptor subfamily 0, group B, member 2Receptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearcholestasiscynarosideethinylestradiolFXRhepatoprotectionNF-κBNrf2

Identifiers

PMID42884083
PMCPMC13665009

What OpenQuestion holds

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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.