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Updated: Jan 13, 2026

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A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
Published on: May 16, 2020
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THE PROTECTIVE EFFECT OF MILK OF THISTLE AGAINST DOXORUBICIN OR METHOTREXATE INDUCED CARDIOTOXICITY
S Othman1, A Abdulsallam2, M Khalaf3
11Department of Pharmacology, College of Medicine, University of Mosul, Iraq.
Georgian Medical News
|January 9, 2026
Summary
Milk thistle extract (MTE) shows significant cardioprotection against Doxorubicin (DOX) and Methotrexate (MXT) chemotherapy. MTE pretreatment preserves cardiac architecture and reduces inflammation, offering a potential strategy to mitigate cardiotoxicity in cancer patients.
Area of Science:
- Cardiovascular Research
- Pharmacology
- Oncology
Background:
- Doxorubicin (DOX) and Methotrexate (MXT) are vital anticancer drugs with dose-limiting cardiotoxicity.
- Milk thistle extract (MTE) possesses known antioxidant and cytoprotective effects.
Purpose of the Study:
- To investigate the protective role of MTE against DOX- or MXT-induced cardiac damage in a rat model.
- To evaluate MTE's efficacy in preventing chemotherapy-induced cardiotoxicity.
Main Methods:
- A 7-day study involving 35 rats divided into five groups: control, DOX alone, MXT alone, DOX+MTE, and MXT+MTE.
- Administration of DOX (IP) or MXT (oral) with or without MTE (oral).
- Histopathological examination of cardiac tissue at the study's conclusion.
Main Results:
- DOX and MXT induced significant cardiotoxicity, characterized by inflammation and structural damage.
- MTE pretreatment substantially protected cardiac architecture against chemotherapy-induced damage.
- Reduced inflammatory cell infiltration was observed in MTE-treated groups.
Conclusions:
- MTE demonstrates marked cardioprotective potential when co-administered with DOX or MXT.
- MTE effectively reduces chemotherapy-induced cardiac inflammation and tissue damage.
- MTE may serve as a valuable adjunct therapy to prevent cardiac complications in cancer patients receiving DOX or MXT.
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