Evidence map›Paper›PMID 37074505›Full record

ArticleMolecular and cellular biochemistry2024

Cardioprotective role of a magnolol and honokiol complex in the prevention of doxorubicin-mediated cardiotoxicity in adult rats.

Irem Aktay, Ceylan Verda Bitirim, Yusuf Olgar, Aysegul Durak, Erkan Tuncay, Deniz Billur, Kamil Can Akcali, Belma Turan

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Pharmaceuticals (Basel, Switzerland) · 2025
    Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Cardioprotective Potential ofCurrent pharmaceutical biotechnology · 2025
    Article
  9. Article
  10. 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

8 authors at 1 institution in 1 country.

Irem AktayDepartment of Biophysics, Faculty of Medicine, Ankara University, Ankara, Turkey.
Ceylan Verda BitirimStem Cell Institute, Ankara University, Ankara, Turkey.
Yusuf OlgarDepartment of Biophysics, Faculty of Medicine, Ankara University, Ankara, Turkey.
Aysegul DurakDepartment of Biophysics, Faculty of Medicine, Ankara University, Ankara, Turkey.
Erkan TuncayDepartment of Biophysics, Faculty of Medicine, Ankara University, Ankara, Turkey.
Deniz BillurDepartment of Histology and Embryology, Faculty of Medicine, Ankara University, Ankara, Turkey.
Kamil Can AkcaliDepartment of Biophysics, Faculty of Medicine, Ankara University, Ankara, Turkey.
Belma TuranDepartment of Biophysics, Faculty of Medicine, Ankara University, Ankara, Turkey. belma.turan@medicine.ankara.edu.tr.ORCID http://orcid.org/0000-0003-2583-9294
Ankara University · TR

Funding

This work is supported by Lokman Hekim University Scientific Research Projects Coordination Unit. Project Number: 202AP404, 2022.
6 · The paper itself

Abstract

Doxorubicin (DOXO) induces marked cardiotoxicity, though increased oxidative stress while there are some documents related with cardioprotective effects of some antioxidants against organ-toxicity during cancer treatment. Although magnolia bark has some antioxidant-like effects, its action in DOXO-induced heart dysfunction has not be shown clearly. Therefore, here, we aimed to investigate the cardioprotective action of a magnolia bark extract with active component magnolol and honokiol complex (MAHOC; 100 mg/kg) in DOXO-treated rat hearts. One group of adult male Wistar rats was injected with DOXO (DOXO-group; a cumulative dose of 15 mg/kg in 2-week) or saline (CON-group). One group of DOXO-treated rats was administered with MAHOC before DOXO (Pre-MAHOC group; 2-week) while another group was administered with MAHOC following the 2-week DOXO (Post-MAHOC group). MAHOC administration, before or after DOXO, provided full survival of animals during 12-14 weeks, and significant recoveries in the systemic parameters of animals such as plasma levels of manganese and zinc, total oxidant and antioxidant statuses, and also systolic and diastolic blood pressures. This treatment also significantly improved heart function including recoveries in end-diastolic volume, left ventricular end-systolic volume, heart rate, cardiac output, and prolonged P-wave duration. Furthermore, the MAHOC administrations improved the structure of left ventricles such as recoveries in loss of myofibrils, degenerative nuclear changes, fragmentation of cardiomyocytes, and interstitial edema. Biochemical analysis in the heart tissues provided the important cardioprotective effect of MAHOC on the redox regulation of the heart, such as improvements in activities of glutathione peroxidase and glutathione reductase, and oxygen radical-absorbing capacity of the heart together with recoveries in other systemic parameters of animals, while all of these benefits were observed in the Pre-MAHOC treatment group, more prominently. Overall, one can point out the beneficial antioxidant effects of MAHOC in chronic heart diseases as a supporting and complementing agent to the conventional therapies.

Indexed as

Allyl CompoundsAntioxidantsBiphenyl CompoundsCardiotoxicityLignansPhenolsAnimalsDoxorubicinMaleMyocytes, CardiacOxidative StressRatsRats, WistarAllyl CompoundsAntioxidantsBiphenyl CompoundsDoxorubicinhonokiolLignansmagnololPhenolsAntioxidantsCardiac dysfunctionCardiotoxicityElectrocardiogramOxidative stressP-waves

Identifiers

PMID37074505
OpenAlexW4366352252

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.