Key result
Adriamycin exerts positive chronotropic and inotropic effects in isolated hearts, completely blocked by dl-propranolol.
Why the study?
Adriamycin is clinically known to produce electrocardiographic abnormalities as side effects, but its genetic mechanism and effects on myocardial contractile force and action potential were unclear.
Does adriamycin affect myocardial contractile force and transmembrane action potential in isolated guinea pig hearts?
Does adriamycin affect myocardial contractile force and transmembrane action potential in isolated guinea pig hearts?
Adriamycin induces positive chronotropic and inotropic effects and shortens action potential duration in isolated guinea pig hearts, which are blocked by propranolol, suggesting beta-adrenergic involvement in its acute cardiotoxicity.
Answers are grounded in this paper and cite their sources.
May implicate β-adrenergic pathways in acute effects; leaves open human cardiotoxicity relevance.
New antitumor antibiotic adriamycin, chemically glycoside linkage of the red pigmented aglycone and the water soluble aminosugar, has been clinically known to produce some electrocardiographic abnormalities such as sinus tachycardia, ST segment depression and the flattening of T wave, as its side effect. In order to clarify its genetic mechanism, isolated guinea pig heart perfused by Langendorff's technique was used and single shot of adriamycin into this preparation produced positive chronotropic and inotropic actions and the acceleration of the repolarization process manifested by the shortening of the duration of the membrane action potential, especially, the repolarization phase 2. This agent has lesser degree of acute accumulative effect in producing arrhythmia, as compared with the action of daunomycin. These effects were completely blocked by dl-propranolol.
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Kobayashi et al. (1972) studied this question. Adriamycin vs. Baseline was evaluated on Myocardial contractile force, heart rate, and transmembrane action potential duration. Adriamycin produced positive chronotropic and inotropic actions and shortened the duration of the membrane action potential in isolated guinea pig hearts, effects that were completely blocked by dl-propranolol.
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