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The acute effects of different spironolactone doses on cardiac function in streptozotocin-induced diabetic rats. | LitMetric

AI Article Synopsis

  • Cardiovascular diseases are the top global cause of death, with diabetes increasing cardiovascular issues; a study showed that mineralocorticoid receptor antagonists can enhance heart function in diabetic patients.
  • This research tested the effects of spironolactone on heart function in rats with diabetes induced by streptozotocin, comparing responses in diabetic rats to healthy ones.
  • Results indicated that higher doses of spironolactone improved heart function in healthy rats, while diabetic rats showed similar benefits from both low and high doses.

Article Abstract

Currently, cardiovascular diseases are the leading cause of global mortality, while diabetes mellitus remains an important cause of cardiovascular morbidity. A recent study showed that patients with diabetes mellitus treated with mineralocorticoid receptor antagonists have improved coronary microvascular function, leading to improved diastolic dysfunction. In this study, we evaluated the influence of acute administration of spironolactone on myocardial function in rats with streptozotocin-induced diabetes mellitus, with special emphasis on cardiodynamic parameters in diabetic rat hearts. The present study was carried out on 40 adult male Wistar albino rats (8 weeks old). Rats were randomly divided into 4 groups (10 animals per group): healthy rats treated with 0.1 μmol/L of spironolactone, diabetic rats treated with 0.1 μmol/L of spironolactone, healthy rats treated with 3 μmol/L of spironolactone, and diabetic rats treated with 3 μmol/L of spironolactone. Different, dose-dependent, acute responses of spironolactone treatment on isolated, working diabetic and healthy rat heart were observed in our study. In healthy rats, better systolic function was achieved with higher spironolactone dose, while in diabetic rats, similar effects of low and high spironolactone dose were observed.

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Source
http://dx.doi.org/10.1139/cjpp-2017-0055DOI Listing

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