Targeting mitochondrial dysfunction and apoptosis in 5-fluorouracil–induced cardiotoxicity using kaempferol-mediated selenium nanoparticles
Abstract 5-Flurouracil (5-FU) is still considered as one of the most popular antimetabolite chemotherapy drugs to treat a wide variety of solid tumors. Dose limiting toxicity on major organs, especially cardiovascular system limits the therapeutic use of 5-FU. The current paper addresses the cardioprotective effect of green synthesized selenium nanoparticles through kaempferol (KMP-SeNPs) on the cardiotoxicity induced by 5-FU in a rat model. 35 male Wistar rats were divided equally into five groups, namely control, 5-FU, Na 2 SeO 3 &5-FU, KMP&5-FU, and KMP-SeNPs&5-FU. The 5-FU consumed 5 days induced cardiotoxicity and there were 21 days of oral treatment. The levels of cardiac injury markers, oxidative stress indices, antioxidant enzymes, inflammatory/anti-inflammatory cytokines and apoptotic markers were measured by ELISA, gene expression and immunohistochemistry. The evaluation of cardiac tissue was done by using histopathology. 5-FU caused significant cardiotoxicity detected by increased cardiac enzymes, oxidative stress, inflammatory cytokines, apoptosis, and extensive histopathologic damage. KMP-SeNPs treatment had a great impact on reducing myocardial injury, normalizing cardiac enzymes, decreasing lipid peroxidation and NO generation, reestablishing antioxidant defenses, and increasing Nrf2 signaling and inhibiting Keap-1 expression. The expression of TNF-α, IL-6, NF-κB, Bax, and caspase-3, were significantly decreased, whereas IL-10, FOXP3, and Bcl-2 showed a significant increase, which is evidence of the great anti-inflammatory, as well as anti-apoptotic effect of KMP-SeNPs. Immunohistochemical and histopathology results supported these molecular and biochemical findings to show approximately normal cardiac architecture. KMP-SeNPs are more effective in protecting against 5-FU-induced cardiotoxicity using antioxidant, anti-inflammatory, immunoregulatory, and anti-apoptotic activities.
Authors
- Moustafa Mahmoud Abdelaziz (ORCID: https://orcid.org/0000-0002-6807-6402)
- Memon Anam Ali (ORCID: https://orcid.org/0009-0000-6846-2402)
- Mohamed H. A. Gadelmawla (ORCID: https://orcid.org/0000-0002-1976-9480)
- Sami Mohamed Nasr (ORCID: https://orcid.org/0000-0001-8683-3131)
- Aya G. Badawy
- Khaled M. Alam-ElDein (ORCID: https://orcid.org/0009-0002-1140-8338)
- Ahmed Mahmoud Gad
- Nouran H. Hindam
- Mai Rabea Mohamed
- Shahd Abdelsalam Taha
Institutions
- Badr University in Cairo (EG)
- Theodor Bilharz Research Institute (EG)
Publication Details
- Journal
- Scientific Reports
- Published
- 2026-09-12
- DOI
- https://doi.org/10.1038/s41598-026-69038-9
- Primary Topic
- Chemotherapy-induced organ toxicity mitigation
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Science and Technology Development Fund