Key result
Doxorubicin dose-dependently alters rat lipid peroxidation and causes venous hyperemia with increased cardiomyocytic cross striation.
Why the study?
Does doxorubicin induce lipid peroxidation and alter heart histology in a rat model?
Does doxorubicin induce lipid peroxidation and alter heart histology in a rat model?
Doxorubicin induces dose-dependent alterations in lipid peroxidation and causes histological myocardial damage in a rat model.
High-dose doxorubicin raises oxidative markers while low-dose reduces them with myocardial changes in rats; leaves open translation to human cardiotoxicity monitoring.
Anthracycline antibiotic doxorubicin, which has proven cardiovascular toxicity, is often used in the treatment of cancer. The research project was carried out in 21 sexually mature Wistar male rats divided into three groups: control group, high-dose experimental group, in which rats were once injected intraperitoneally with doxorubicin hydrochloride at a dose of 10 mg/kg and low-dose experimental group, in which animals twice received intraperitoneal 2.5 mg/kg doses of doxorubicinhydrochloride at 10-day interval.An increase of malondialdehyde was revealed in the membranes of red blood cells in the high-dose experimental group, while in the low-dose experimental group a reduction in the levels of malondialdehyde and plasma hydroperoxides as well as a decreasing of catalase activity was observed. Intake of doxorubicin also causes venous hyperemia in wide areas of myocardiumalong with increasing of cardiomyocytic cross striation.
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Джиоев et al. (2015) studied Cardiovascular toxicity (n=21). Doxorubicin hydrochloride vs. Control group was evaluated on Lipid peroxidation (malondialdehyde, plasma hydroperoxides, catalase activity) and heart histology. Doxorubicin administration in rats altered lipid peroxidation dose-dependently and caused venous hyperemia along with increased cardiomyocytic cross striation.
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