Liraglutide ameliorated methotrexate-induced cardiotoxicity in rats through anti-inflammatory and antioxidant pathway modulation, adding chemo-cardioprotection to GLP-1 benefits.
Key findingLiraglutide ameliorated methotrexate-induced cardiotoxicity in rats through anti-inflammatory and an
What the researchers found
Liraglutide ameliorated methotrexate-induced cardiotoxicity in rats through anti-inflammatory and antioxidant pathway modulation, adding chemo-cardioprotection to GLP-1 benefits.
Why it matters
These findings have practical implications for the growing number of patients using peptide-based therapies.
The numbers in context
Four groups of rats tested. Methotrexate given as single dose of 20 mg/kg. Two different liraglutide doses evaluated for cardioprotection.
How the study worked
Study methodology detailed in the full publication.
Who was studied
Rats receiving methotrexate with or without liraglutide cardioprotection
What this study cannot tell us
Study limitations in the full publication.
How to read the evidence
Evidence level based on study design in publication.
When this study was published
Published in 2025.
The bigger picture
This study contributes to the expanding evidence for peptide therapeutics in clinical practice.
Questions still open
- What are the long-term implications?
- How do results compare to other evidence?
- What further research is needed?
Common questions
What does this mean for patients?
How reliable is this?
Read the original research
Liraglutide Ameliorates Methotrexate-Induced Cardiotoxicity in Rats: Modulation of Oxidative Stress, Autophagy, and the TNF-α/NF-κB Signaling Inflammatory Pathway.
Journal of biochemical and molecular toxicology, 39(12), e70606
Citation
Ali, Dina A; Ibrahim, Dalia; Kolieb, Eman; Abdel Fattah, Islam O; Maher, Shymaa A; Elkelish, Amr; Abdalneim, Nasir A; Abozied, Nadia. (2025). Liraglutide Ameliorates Methotrexate-Induced Cardiotoxicity in Rats: Modulation of Oxidative Stress, Autophagy, and the TNF-α/NF-κB Signaling Inflammatory Pathway.. Journal of biochemical and molecular toxicology, 39(12), e70606. https://doi.org/10.1002/jbt.70606