Key result
Aliskiren pretreatment significantly protected against doxorubicin-induced enzymatic changes and cardiac tissue damage in rats.
Why the study?
Does aliskiren prevent doxorubicin-induced acute cardiomyopathy in rats?
Does aliskiren prevent doxorubicin-induced acute cardiomyopathy in rats?
Aliskiren pretreatment protects against doxorubicin-induced acute cardiomyopathy and enzymatic changes in a rat model.
Hypothesis-generating for aliskiren cardioprotection; requires human trials before any clinical consideration.
In this study, effect of aliskiren (ALK) on doxorubicin (DXR)-induced cardiomyopathy in rats was evaluated. ALK (50 and 100 mg/kg/day) was administered for 7 days and a single intraperitoneal injection of DXR (20 mg/kg) on day 5. The animals were sacrificed 48 h after DXR administration. DXR produced significant elevation in malondialdehyde (MDA) and significantly inhibited the activity of glutathione (GSH) in heart tissue, with a significant rise in the serum levels of lactate dehydrogenase (LDH), total cholesterol (TC), triglycerides (TG), low-density lipoprotein (LDL) and reduction in high-density lipoprotein (HDL), indicating acute cardiac toxicity. ALK pretreatment significantly reduced the MDA concentration and ameliorated the inhibition of cardiac GSH activity. ALK also significantly improved the serum levels of LDH, TC, TG, LDL and reduction in HDL in DXR-treated rats. Furthermore, histological examination of the heart sections confirmed the myocardial injury with DXR administration and the near-normal pattern with ALK pretreatment. The results provide clear evidence that the ALK pretreatment offered significant protection against DXR-induced enzymatic changes and cardiac tissue damage.
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Najmi et al. (2010) studied Doxorubicin-induced acute cardiomyopathy. Aliskiren vs. Doxorubicin alone was evaluated on Cardiac toxicity markers (MDA, GSH, LDH, TC, TG, LDL, HDL) and histological myocardial injury. Aliskiren pretreatment significantly protected against doxorubicin-induced enzymatic changes and cardiac tissue damage in rats.
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