Comparison of Cardioprotective Effects of Dapagliflozin and Trimetazidine in the Model of Doxorubicin-Cyclophosphamide Cardiotoxicity

Background: Data published by task groups of the Ministry of Health of the Russian Federation, the European Society of Cardiology, and other medical associations and institutions show that chemotherapy-induced cardiomyopathy is still a challenging issue that requires further research. Objective: To...

Full description

Saved in:
Bibliographic Details
Published inInnovacionnaâ medicina Kubani (Online) no. 4; pp. 6 - 14
Main Authors Avagimyan, A. A., Trofimenko, A. I., Sheibani, M., Kakturskiy, L. V., Urazova, O. I., Navasardyan, G. A., Jndoyan, Z. T., Sulashvili, N. V., Gabunia, L. I., Gorgaslidze, N. S., Khamidova, F. M., Martemyanova, L. A., Pogosova, N. V., Sarrafzadegan, N.
Format Journal Article
LanguageEnglish
Russian
Published Scientific Research Institute, Ochapovsky Regional Clinical Hospital no. 1 15.11.2023
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background: Data published by task groups of the Ministry of Health of the Russian Federation, the European Society of Cardiology, and other medical associations and institutions show that chemotherapy-induced cardiomyopathy is still a challenging issue that requires further research. Objective: To compare the cardioprotective potential of trimetazidine and dapagliflozin in a rat model of doxorubicin-cyclophospha-mide cardiomyopathy. Materials and methods: Our randomized in vivo experimental study included 80 Wistar female rats. Doxorubicin and cyclophosphamide were administered at a dose of 15 mg/kg and 150 mg/kg, respectively. Trimetazidine (42 mg/kg) and dapagliflozin (14 mg/kg) were additionally administered to groups 3 and 4, respectively. The total duration of the experiment was 14 days. Results: Doxorubicin+cyclophosphamide mode of chemotherapy induces the development of toxic-ischemic cardiomyopathy. The trimetazidine and dapagliflozin administration was accompanied by stabilization of cardiovascular parameters. Comparison of both drugs’ cardioprotective properties revealed a clear advantage of dapagliflozin over trimetazidine, especially in terms of such an important indicator as N-terminal pro-B-type natriuretic peptide. Conclusions: Further research aimed at exploring the cardioprotective potential of dapagliflozin against cardiovascular complications of chemotherapy is justified from a pathogenetic point of view.
ISSN:2541-9897
2541-9897
DOI:10.35401/2541-9897-2023-8-4-6-14