Key result
Ellagic acid significantly prevented doxorubicin-induced increase in heart rate (p < 0.001) and increased single contraction force (p < 0.001) in a rat model of cardiovascular toxicity.
Why the study?
Doxorubicin causes cardiovascular toxicity, while ellagic acid exhibits antioxidant properties and protects against cardiovascular diseases, prompting investigation into its potential protective effects.
Does ellagic acid prevent doxorubicin-induced cardiovascular toxicity in Wistar rats?
Does ellagic acid prevent doxorubicin-induced cardiovascular toxicity in Wistar rats?
Ellagic acid attenuates doxorubicin-induced functional and morphological cardiac changes in a rat model, suggesting potential cardioprotective effects.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating in rat models; human trials required before clinical consideration.
Doxorubicin is an anticancer agent that is commonly used to treat a number of tumors and is associated with acute and chronic changes of the cardiovascular system. Ellagic acid has strong free radical scavenging capacity, neuroprotective and hepatoprotective effects, and is known to protect against changes occurring due to diabetes, cardiovascular diseases, and cancer. Twenty-four Wistar rats were divided in four groups: control group received saline, doxorubicin group received doxorubicin in a single dose of 20 mg/kg, ellagic acid group received ellagic acid in a dose of 4 mg/kg, and doxorubicin + ellagic acid group received doxorubicin and ellagic acid in same doses as in previous groups. The effect of ellagic acid treatment, alone or in combination with doxorubicin, was studied on isolated heart frequency and strength of the contraction, and on thoracic aorta contractile responses. Application of ellagic acid to rats pre-treated with doxorubicin significantly prevented functional changes occurring in the heart, but not in the thoracic aorta tissue. Ellagic acid statistically significantly (p < 0.001) prevented doxorubicin-induced increase in heart rate, while at the same time increased single contraction force (p < 0.001) and attenuated morphological changes on heart tissue induced by doxorubicin. We can conclude that ellagic acid has potential to prevent doxorubicin-induced changes of the cardiovascular system.
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Šalinger-Martinović et al. (2021) studied Doxorubicin-induced cardiovascular toxicity (n=24). Ellagic acid vs. Doxorubicin alone, saline control, and ellagic acid alone was evaluated on Isolated heart frequency and strength of contraction (p=< 0.001). Ellagic acid significantly prevented doxorubicin-induced increase in heart rate (p < 0.001) and increased single contraction force (p < 0.001) in a rat model of cardiovascular toxicity.
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