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The differential effects of green tea on dose-dependent doxorubicin toxicity
Slawomir Mandziuk1, Renata Gieroba2, Agnieszka Korga3
1Department of Pneumology, Oncology and Alergology, Medical University of Lublin, Lublin, Poland.
Background:
Doxorubicin (DOX) is an anticancer drug displaying cardiac and hepatic adverse effects mostly dependent on oxidative stress. Green tea (GT) has been reported to play a protective role in diseases resulting from oxidative stress.
Objective:
The objective of this study was to evaluate if GT protects against DOX-induced oxidative stress, heart and liver morphological changes, and metabolic disorders.
Methods:
Male Wistar rats received intraperitoneal injection of DOX (1.0 or 2.0 mg/kg b.w.) for 7 weeks or concomitantly GT extract soluble in drinking water.
Results:
There were multidirectional effects of GT on blood metabolic parameters changed by DOX. Among all tested biochemical parameters, statistically significant protection of GT against DOX-induced changes was revealed in case of blood fatty acid-binding protein, brain natriuretic peptide, and superoxide dismutase.
Conclusion:
DOX caused oxidative stress in both organs. It was inhibited by GT in the heart but remained unchanged in the liver. DOX-induced general toxicity and histopathological changes in the heart and in the liver were mitigated by GT at a higher dose of DOX and augmented in rats treated with a lower dose of the drug.
Insights
Green tea extract partially protected against doxorubicin toxicity, reducing oxidative stress and improving heart and liver health in rats. However, effects varied with doxorubicin dosage.
Area of Science:
- Pharmacology and Toxicology
- Natural Product Chemistry
- Cardiovascular and Hepatic Medicine
Background:
- Doxorubicin (DOX), a potent anticancer agent, induces cardiotoxicity and hepatotoxicity primarily through oxidative stress.
- Green tea (GT) possesses antioxidant properties and has shown protective effects against oxidative stress-related conditions.
Purpose of the Study:
- To investigate the protective potential of green tea extract against doxorubicin-induced oxidative stress.
- To evaluate the effects of green tea on doxorubicin-induced cardiac and hepatic morphological and metabolic alterations.
Main Methods:
- Male Wistar rats were administered doxorubicin (1.0 or 2.0 mg/kg b.w.) intraperitoneally for 7 weeks.
- Concomitant administration of green tea extract in drinking water was performed.
- Biochemical parameters, including blood fatty acid-binding protein, brain natriuretic peptide, and superoxide dismutase, were assessed.
Main Results:
- Green tea extract demonstrated significant protective effects on specific biomarkers, including blood fatty acid-binding protein, brain natriuretic peptide, and superoxide dismutase, against doxorubicin-induced changes.
- Multidirectional effects of green tea were observed on doxorubicin-altered blood metabolic parameters.
- Oxidative stress induced by doxorubicin was inhibited by green tea in the heart but not in the liver.
Conclusions:
- Green tea extract mitigated doxorubicin-induced general toxicity and histopathological damage in the heart and liver, particularly at a higher doxorubicin dose.
- The protective efficacy of green tea against doxorubicin toxicity was dose-dependent and organ-specific.
- Further research is warranted to elucidate the precise mechanisms underlying green tea's protective effects and its clinical applicability.
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