Key result
Metoprolol, pilocarpine, and diltiazem significantly prevented hypoglycemia-induced QTc interval prolongation compared to the insulin-saline control group (121.6, 116.6, and 129.0 msec vs 143.8 msec, respectively).
Why the study?
Insulin-induced hypoglycemia prolongs the QTc interval, which can cause fatal ventricular arrhythmias in diabetic patients, prompting evaluation of metoprolol, diltiazem, and pilocarpine to prevent this prolongation.
Does metoprolol, diltiazem, or pilocarpine prevent hypoglycemia-induced QTc prolongation in male rats?
Does metoprolol, diltiazem, or pilocarpine prevent hypoglycemia-induced QTc prolongation in male rats?
Answers are grounded in this paper and cite their sources.
Metoprolol, pilocarpine, and diltiazem effectively prevented hypoglycemia-induced QTc prolongation in a rat model, suggesting potential prophylactic utility against pro-arrhythmic effects of insulin-induced hypoglycemia.
Background Insulin-induced hypoglycemia has been demonstrated to prolong the corrected QT (QTc) interval. Prolongation of the QTc interval, especially in diabetic patients using insulin, can cause fatal ventricular arrhythmias. The aim of this study was to evaluate the effects of metoprolol, diltiazem, and pilocarpine on hypoglycemia-induced QTc prolongation. Methods Thirty male rats were randomly distributed into the following five groups: Group 1 (1 mL/kg saline, n=6), Group 2 (40 U/kg crystalline insulin + saline, n=6), Group 3 (40 U/kg crystalline insulin + 1 mg/kg metoprolol, n=6), Group 4 (40 U/kg crystalline insulin + 0.8 mg/kg pilocarpine, n=6), and Group 5 (40 U/kg crystalline insulin + 2 mg/kg diltiazem, n=6). Three hours after insulin injection, the blood glucose level was measured in all groups. Blood glucose <40 mg/dl was defined as hypoglycemia. Electrocardiograms (ECG) were taken in lead I (DI), and QTc was calculated by using Bazett's formula. Results Group 2 (insulin + saline) showed that it had a significantly prolonged QTc interval as compared to the control group (p<0.0001). However, treatments of the rats with metoprolol, pilocarpine, and diltiazem significantly prevented prolongation of the QTc interval as compared to the insulin + saline group (p<0.005, p<0.005, and p<0.01, respectively). Conclusion The findings of the present study demonstrated the efficacy of metoprolol, pilocarpine, and diltiazem in the prevention of hypoglycemia-induced QTc prolongation in male rats.
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Çağıltay et al. (2021) studied Hypoglycemia-induced QTc prolongation (n=30). Metoprolol, Pilocarpine, and Diltiazem vs. Insulin + saline was evaluated on QTc interval (p=<0.005). Metoprolol, pilocarpine, and diltiazem significantly prevented hypoglycemia-induced QTc interval prolongation compared to the insulin-saline control group (121.6, 116.6, and 129.0 msec vs 143.8 msec, respectively).
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