Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Feb;25(2):193-204.
doi: 10.1007/s12012-024-09958-y. Epub 2025 Jan 26.

Cardiotoxicity Associated With a Low Doses of 5-FU Promotes Morphoquantitative Changes in the Intrinsic Cardiac Nervous System

Affiliations

Cardiotoxicity Associated With a Low Doses of 5-FU Promotes Morphoquantitative Changes in the Intrinsic Cardiac Nervous System

Karile Cristina da Costa Salomão et al. Cardiovasc Toxicol. 2025 Feb.

Abstract

5-Fluorouracil (5-FU) is a chemotherapeutic that is used to treat solid tumors. However, 5-FU is associated with several side effects, including cardiotoxicity. Considering the importance of the intrinsic cardiac nervous system (ICNS) for the heart and that little is known about effects of 5-FU on this nervous system plexus, the purpose of the present study was to evaluate effects 5-FU at a low dose on the ICNS and oxidative and inflammatory effects in the heart in Wistar rats. The rats were divided into two groups: treated and 5-FU (n = 6/group). The control group received saline only. The treated group received the following clinical doses of 5-FU: 15 mg/kg for 4 consecutive days, followed by 6 mg/kg for 4 days alternated with non-treatment days, and finally 15 mg/kg as the last dose on day 14. On day 15, the rats were euthanized and underwent thoracotomy. The atria were used for histological analysis, and the ventricles were used for biochemical analysis. The results showed an increase in neuronal density and a decrease in ganglionic and neuronal area in the ICNS. Furthermore, tissue inflammation was observed, indicated by an increase in proinflammatory factors and the enzymatic activity of myeloperoxidase and n-acetyl-glucosaminidase. Oxidative stress was also observed, confirmed by a reduction of endogenous antioxidant defenses and the presence of lipoperoxidation. Treatment with 5-FU also caused cardiac atrophy and fibrosis. These findings indicate that cardiotoxicity is present with 5-FU treatment and affects the morphometric aspects of the ICNS.

Keywords: Cardiac plexus; Fibrosis; Heart; Inflammation; Neurons; Oxidative stress.

PubMed Disclaimer

Conflict of interest statement

Declarations. Conflict of Interest: The authors have no conflicts of interest to declare that are relevant to the content of this article. Ethical Statement: The animal study protocol was approved by the Committee for Ethical Conduct in the Use of Animals in Experimentation of the State University of Maringa/ Parana—Brazil (CEUA, n° 4422140918).

Similar articles

Cited by

References

    1. Aslam, M. S., Naveed, S., Ahmed, A., Abbas, Z., Gull, I., & Athar, M. A. (2014). Side effects of chemotherapy in cancer patients and evaluation of patients opinion about starvation based differential chemotherapy. Journal of Cancer Therapy, 5, 817–822. https://doi.org/10.4236/jct.2014.58089 - DOI
    1. Malet-Martino, M. R., & Martino, M. (2002). Clinical studies of three oral prodrugs of 5-fluorouracil (capecitabine, UFT, S-1): A review. The Oncologist, 7(4), 288–323. - DOI - PubMed
    1. Jatto, J., Oboh, E., & Ntekim, A. (2017). 5-Fluorouracil induced cardiotoxicity in a young patient with colon cancer: An unusual finding. Journal of Oncology Research and Therapy. https://doi.org/10.29011/2574-710X - DOI
    1. Alnaim, L. (2010). Individualization of 5-fluorouracil in the treatment of colorectal cancer. SRX Pharmacology. https://doi.org/10.3814/2010/352491 - DOI
    1. Arias, J. L. (2008). Novel strategies to improve the anticancer action of 5-fluorouracil by using drug delivery systems. Molecules, 13, 2340–2369. https://doi.org/10.3390/molecules13102340 - DOI - PubMed - PMC

LinkOut - more resources