Investigate if Metoprolol and Troxerutin Could Prevent Cardiotoxicity Mitigated by Doxorubicin

Doxorubicin, which is widely used as an anti-tumour drug, it associated with Cardiotoxic problems. Previous studies suggested that each of the metoprolol and troxerutin alone could provide potential protection against this cardiotoxic effect. This study was aimed to investigate if the combination of these two drugs could provide superior protection against the cardiotoxic effect of doxorubicin. Fifty male Wistar rats were divided into five groups; each group had 10 animals. Both control negative and control positive groups, a treatment group for each drug and a combination group. The blood samples were collected from the animals to extract the serum, and the serums were used in Elisa technique for investigation the concentration of CK-MB, SOD, MDA, IL-6 and TNF-Alpha for all groups to study the effect of the drugs to these markers. The combination treatment group provided a superior effect in almost all groups, The combination treatment group achieved nearly the levels of the control negative group in 2 markers, which were CK-MB and TNF. In oxidative stress markers (MDA) and antioxidant (SOD), it had the lowest concentration of MDA compared to positive group. While highest concentration of antioxidant (SOD) compared to positive group suggesting a slightly better effect of the combination. In conclusion, Combination therapy provides a superior effect on key markers, suggesting its benefits by working on various pathways to protect the heart. Although the effect of the combination was still comparable in oxidative stress markers to other treatment groups, the combination therapy totally outperformed monotherapies.

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Publication Details

Journal
Kufa Journal For Veterinary Medical Sciences
Published
2025-07-14
DOI
https://doi.org/10.36326/kjvs/2025/v16i118663
Primary Topic
Chemotherapy-induced cardiotoxicity and mitigation
Type
article
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article

Investigate if Metoprolol and Troxerutin Could Prevent Cardiotoxicity Mitigated by Doxorubicin

Fouad Zeidan Hamzah, Teeba Ghassan
Kufa Journal For Veterinary Medical Sciences
Chemotherapy-induced cardiotoxicity and mitigation
article

Investigate if Metoprolol and Troxerutin Could Prevent Cardiotoxicity Mitigated by Doxorubicin

Fouad Zeidan Hamzah, Teeba Ghassan
article en

Abstract

Doxorubicin, which is widely used as an anti-tumour drug, it associated with Cardiotoxic problems. Previous studies suggested that each of the metoprolol and troxerutin alone could provide potential protection against this cardiotoxic effect. This study was aimed to investigate if the combination of these two drugs could provide superior protection against the cardiotoxic effect of doxorubicin. Fifty male Wistar rats were divided into five groups; each group had 10 animals. Both control negative and control positive groups, a treatment group for each drug and a combination group. The blood samples were collected from the animals to extract the serum, and the serums were used in Elisa technique for investigation the concentration of CK-MB, SOD, MDA, IL-6 and TNF-Alpha for all groups to study the effect of the drugs to these markers. The combination treatment group provided a superior effect in almost all groups, The combination treatment group achieved nearly the levels of the control negative group in 2 markers, which were CK-MB and TNF. In oxidative stress markers (MDA) and antioxidant (SOD), it had the lowest concentration of MDA compared to positive group. While highest concentration of antioxidant (SOD) compared to positive group suggesting a slightly better effect of the combination. In conclusion, Combination therapy provides a superior effect on key markers, suggesting its benefits by working on various pathways to protect the heart. Although the effect of the combination was still comparable in oxidative stress markers to other treatment groups, the combination therapy totally outperformed monotherapies.

Kufa Journal For Veterinary Medical SciencesVol. 16(1)
University of Kufa (IQ)
Openalex Percentile: Top 67%
Chemotherapy-induced cardiotoxicity and mitigation
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