Key result
Pretreatment with dantrolene at 5 mg/kg substantially reduced peroxidative damage and lowered serum CK-MB, LDH, and AST in rats with acute adriamycin-induced cardiotoxicity.
Hypothesis-generating in rodent adriamycin cardiotoxicity; clinical translation requires prospective human studies.
Possible preventive effect of dantrolene against the peroxidative damage in rat heart which was induced by the administration of an acute dose of adriamycin (ADR, 20 mg/kg, i.p.) has been examined. Forty-eight hours after ADR administration, biochemical changes including the activities of serum creatine kinase isoenzyme (CK-MB), lactate dehydrogenase (LDH) and aspartate aminotransferase (AST) and the levels of malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) in heart tissue were measured. Pretreatment of rats with dantrolene, given i.p. 30 min prior to ADR injection, substantially reduced the peroxidative damage in the myocardium, and markedly lowered the serum CK-MB, LDH and AST. The protective effects obtained by dantrolene administration, however, were not complete and did not reach those of the control group. Dantrolene, at 5 mg/kg, was useful to obtain significant protective effects, while the protector effect of higher dantrolene dosing level (10 mg/kg) was weak or absent. These results suggest that, at least in part, due to antioxidative properties, dantrolene may provide a significant protective effect against acute ADR-induced cardiotoxicity.
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Büyükokuroğlu et al. (2004) studied Acute adriamycin cardiotoxicity. Dantrolene vs. Control group was evaluated on Biochemical changes including serum CK-MB, LDH, AST and heart tissue MDA, SOD, and GSH-Px. Pretreatment with dantrolene at 5 mg/kg substantially reduced peroxidative damage and lowered serum CK-MB, LDH, and AST in rats with acute adriamycin-induced cardiotoxicity.
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