Key result
Ivabradine significantly reduced elevated heart rate, serum cardiac enzymes, oxidative stress, and cardiac tissue damage in mice with doxorubicin-induced acute cardiotoxicity.
Why the study?
Does ivabradine prevent doxorubicin-induced acute cardiotoxicity in mice?
Does ivabradine prevent doxorubicin-induced acute cardiotoxicity in mice?
Answers are grounded in this paper and cite their sources.
In a mouse model, ivabradine protected against doxorubicin-induced acute cardiotoxicity by reducing heart rate, oxidative stress, and nitric oxide production.
Doxorubicin (DOX) has been used in variety of human malignancies for decades. Despite its efficacy in cancer, clinical usage is limited because of its cardiotoxicity, which has been associated with oxidative stress. The possible protective mechanisms of ivabradine, a selective inhibitor of the I(f) channel, against acute doxorubicin cardiotoxicity were investigated in mice. Cardiac toxicity was induced by a single intraperitoneal injection of doxorubicin (15 mg/kg). Ivabradine treatment (10 mg/kg/day, orally) was started 5 days before doxorubicin administration. Ivabradine significantly reduced the elevated heart rate and the serum cardiac enzymes resulted from DOX administration. Also, ivabradine reversed DOX-induced deficits in the antioxidant defense mechanisms, decreased lipid peroxidation in cardiac tissue and attenuated the production of nitric oxide levels by induced nitric oxide synthase enzyme. In addition, DOX-induced cardiac tissue damage observed by histopathological examination was markedly ameliorated with ivabradine. In conclusion, the beneficial effects of ivabradine against DOX induced cardiotoxicity are mediated by the reduction of heart rate with inhibition of oxidative stress and nitric oxide detrimental effects. Original Research Article Boshra and Shalaby; BJMMR, 6(12): 1166-1176, 2015; Article no.BJMMR.2015.295 1167
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Boshra et al. (2015) studied Doxorubicin-induced acute cardiotoxicity. Ivabradine vs. Doxorubicin alone was evaluated on Heart rate, serum cardiac enzymes, and oxidative stress markers. Ivabradine significantly reduced elevated heart rate, serum cardiac enzymes, oxidative stress, and cardiac tissue damage in mice with doxorubicin-induced acute cardiotoxicity.
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