Journal of Experimental Pharmacology (Mar 2024)

Dapagliflozin Pretreatment Prevents Cardiac Electrophysiological Changes in a Diet and Streptozotocin Induction of Type 2 Diabetes in Rats: A Potential New First-Line?

  • Juttla PK,
  • Chege BM,
  • Mwangi PW,
  • Bukachi F

Journal volume & issue
Vol. Volume 16
pp. 123 – 133

Abstract

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Prabhjot Kaur Juttla,1 Boniface Mwangi Chege,2 Peter Waweru Mwangi,1 Frederick Bukachi1 1Department of Medical Physiology, University of Nairobi, Nairobi, Kenya; 2School of Health Sciences, Dedan Kimathi University of Technology, Nyeri, KenyaCorrespondence: Prabhjot Kaur Juttla, Department of Medical Physiology, University of Nairobi, P.O. Box 30197 – 00100, Nairobi, Kenya, Email [email protected]: Dapagliflozin exerts cardioprotective effects in Type 2 Diabetes Mellitus (T2DM). However, whether these effects prevent electrocardiographic changes associated with T2DM altogether remain unknown. Our aim was to investigate the prophylactic effect of dapagliflozin pretreatment on the rat ECG using a high-fat, high-fructose (HFHf) diet and a low dose streptozotocin (STZ) model of T2DM.Methods: Twenty-five (25) rats were randomized into five (5) groups: normal control receiving a normal diet while the other groups received an 8-week HFHf and 40mg/kg STZ on day 42, and either: saline for the diabetic control (1 mg/kg/d), low dose (1.0 mg/kg/d) and high dose dapagliflozin (1.6 mg/kg/d), or metformin (250 mg/kg/d). Oral glucose tolerance (OGT), electrocardiograms (ECGs), paracardial adipose mass, and left ventricular fibrosis were determined. Data were analyzed using GraphPad version 9.0.0.121, with the level of significance at p < 0.05.Results: Compared to the diabetic control group, a high dose of dapagliflozin preserved the OGT (p = 0.0001), QRS-duration (p = 0.0263), QT-interval (p = 0.0399), and QTc intervals (p = 0.0463). Furthermore, the high dose dapagliflozin group had the lowest paracardial adipose mass (p = 0.0104) and fibrotic area (p = 0.0001). In contrast, while metformin showed favorable effects on OGT (p = 0.0025), paracardial adiposity (p = 0.0153) and ventricular fibrosis (p = 0.0291), it did not demonstrate significant antiarrhythmic effects.Conclusion: Pretreatment with higher doses of Dapagliflozin exhibits prophylactic cardioprotective characteristics against diabetic cardiomyopathy that include antifibrotic and antiarrhythmic qualities. This suggests that higher doses of dapagliflozin could be a more effective initial therapeutic option in T2DM.Keywords: electrocardiogram, diabetic cardiomyopathy, sodium glucose co-transporter inhibitors, prophylaxis, animal model

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