Evidence map›Paper›PMID 39850246›Full record

ArticleInternational journal of physiology, pathophysiology and pharmacology2024

Therapeutic effect of coenzyme-Q10 pretreatment on isoprenaline-induced cardiogenic hepatorenal complications in rats.

Emmanuel Onyinyechukwu Chidebe, Emuesiri Goodies Moke, Jerome Ndudi Asiwe, Benneth Ben-Azu, Winifred Eseoghene Demaki, Benjamin Oritsemuelebi, Oke Arighwrode, Akpevboghene Nicholas Avabore, Adrian Itivere Omogbiya, Anthony Taghogho Eduviere and 1 more

Abstract read
In one paragraph

Article in International journal of physiology, pathophysiology and pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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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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

1 citing paper in PubMed.

  1. Cardioprotective and Antioxidant Effects of Marine-DerivedPharmaceuticals (Basel, Switzerland) · 2026
    Article
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

11 authors.

Emmanuel Onyinyechukwu ChidebeDepartment of Pharmacology, Faculty of Basic Medical Sciences, Delta State University Abraka, Nigeria.
Emuesiri Goodies MokeDepartment of Pharmacology, Faculty of Basic Medical Sciences, Delta State University Abraka, Nigeria.
Jerome Ndudi AsiweDepartment of Human Physiology, Faculty of Basic Medical Sciences, Delta State University Abraka, Nigeria.
Benneth Ben-AzuDepartment of Pharmacology, Faculty of Basic Medical Sciences, Delta State University Abraka, Nigeria.
Winifred Eseoghene DemakiDepartment of Pharmacology, Faculty of Basic Medical Sciences, Delta State University Abraka, Nigeria.
Benjamin OritsemuelebiDepartment of Pharmacology, Faculty of Basic Medical Sciences, Delta State University Abraka, Nigeria.
Oke ArighwrodeDepartment of Human Anatomy and Cell Biology, Faculty of Basic Medical Sciences, Delta State University Abraka, Nigeria.
Akpevboghene Nicholas AvaboreDepartment of Human Anatomy and Cell Biology, Faculty of Basic Medical Sciences, Delta State University Abraka, Nigeria.
Adrian Itivere OmogbiyaDepartment of Pharmacology, Faculty of Basic Medical Sciences, Delta State University Abraka, Nigeria.
Anthony Taghogho EduviereDepartment of Pharmacology, Faculty of Basic Medical Sciences, Delta State University Abraka, Nigeria.
Emuesiri Kohworho UmukoroDepartment of Pharmacology and Therapeutics, Faculty of Basic Clinical Sciences, Delta State University Abraka, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe significant correlation between acute myocardial infarction and subsequent hepatorenal dysfunction could result in a higher mortality rate in patients. The study aimed to evaluate the effect and mechanisms of coenzyme-Q10 (Q10) administration on hepatorenal dysfunction in an isoprenaline (ISO)-induced myocardial infarction model in rats. MATERIALS AND

methodsTwenty male rats were assigned into four groups (n = 5). Groups 1-2 were administered intraperitoneally with normal saline, groups 3-4 were pretreated with Q10 (10 mg/kg, i.p.) for 28 days, and groups 2 and 4 received ISO (200 mg/kg, i.p.) on the last two days. Body, kidney, and liver weights, antioxidants and biochemical biomarkers, and histopathological investigation of the liver and kidney tissues were performed.

resultsThe administration of ISO significantly (P < 0.05) increased oxidative stress and altered the liver and renal function integrity and morphology. Pretreatment with Q10 demonstrated a protective effect against biochemical and histological alterations through significantly enhanced antioxidant actions, notably increasing the levels of superoxide dismutase, catalase, glutathione, and glutathione transferase; reduced liver enzymes (aspartate transaminase, aspartate aminotransferase, alkaline phosphatase, and lactate dehydrogenase), decreased urea and creatinine concentrations and reduced the gravity of histomorphological changes in hepatic and renal tissues of ISO treated rats.

conclusionOverall, our result suggests that Q10 confers hepatic and renal protection against ISO-induced hepatorenal dysfunction accompanying myocardial infarction through its antioxidant effects and amelioration of fibrotic changes.

Indexed as

antioxidantcoenzyme-Q10hepatorenal dysfunctionIsoprenalinemyocardial infarction

Identifiers

PMID39850246
PMCPMC11751547

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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.