Why the study?
Does doxorubicin cause delayed cardiotoxicity via interference with cardiac beta-adrenoceptor function in rats?
Does doxorubicin cause delayed cardiotoxicity via interference with cardiac beta-adrenoceptor function in rats?
Delayed cardiotoxicity induced by doxorubicin in rats is not mediated by interference with cardiac beta-adrenoceptor function.
Doxorubicin cardiotoxicity occurs without beta-adrenoceptor blockade in rats; challenges this mechanism and leaves open alternatives for study.
The possible relationship between the effect of the anthracycline-cytostatic doxorubicin (Dox) on the cardiac beta-adrenoceptor function in vitro and the development of delayed cardiotoxicity in vivo has been investigated in the rat. Dox (10(-5)-10(-4) M) blocked the chronotropic effect of isoprenaline on isolated atria in a competitive manner. Treatment with a single dose of Dox 5 mg/kg intravenously caused marked ECG changes manifested by progressive prologations of the Q alpha T and S alpha T-intervals, which amounted to 37% and 58% respectivity 5 weeks after the medication. At this time no beta-blocking action was detectable when tested on the isolated atria in the same rats. The results indicate that the delayed cardiotoxicity induced by Dox is not mediated by an interference with the cardiac beta-adrenoceptor function.
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Rasmussen et al. (1989) studied this question.
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