Groop L, Tötterman K J
Acta Endocrinol (Copenh). 1982 Jul;100(3):410-5. doi: 10.1530/acta.0.1000410.
In a double-blind cross-over trial we compared the effects of placebo and propranolol on iv tolbutamide and oral glipizide-stimulated insulin secretion in 10 non-insulin dependent diabetics. The patients were randomly allocated for 2 weeks treatment with placebo and propranolol 80 mg twice daily. At the end of each period an iv tolbutamide test and an oral glipizide-glucose-test were performed. Tolbutamide-stimulated insulin secretion was not affected by propranolol. There was no change in blood glucose levels during the iv tolbutamide test (IVTT), which excluded an effect of blood glucose on insulin secretion. During the oral glipizide-glucose challenge propranolol decreased blood glucose at 60 min (P less than 0.01) and increased C-peptide at 0 min (P less than 0.01) and 30 min (P less than 0.05) compared with placebo. In contrast to earlier results obtained in animals and healthy subjects propranolol does not inhibit insulin- or C-peptide responses to sulphonylurea in patients with non-insulin dependent diabetes mellitus.
在一项双盲交叉试验中,我们比较了安慰剂和普萘洛尔对10名非胰岛素依赖型糖尿病患者静脉注射甲苯磺丁脲和口服格列吡嗪刺激的胰岛素分泌的影响。患者被随机分配接受为期2周的安慰剂和每日两次80毫克普萘洛尔治疗。在每个阶段结束时,进行静脉注射甲苯磺丁脲试验和口服格列吡嗪-葡萄糖试验。甲苯磺丁脲刺激的胰岛素分泌不受普萘洛尔影响。静脉注射甲苯磺丁脲试验(IVTT)期间血糖水平无变化,这排除了血糖对胰岛素分泌的影响。与安慰剂相比,在口服格列吡嗪-葡萄糖激发试验中,普萘洛尔在60分钟时降低了血糖(P<0.01),并在0分钟(P<0.01)和30分钟(P<0.05)时增加了C肽。与先前在动物和健康受试者中获得的结果相反,普萘洛尔并不抑制非胰岛素依赖型糖尿病患者对磺脲类药物的胰岛素或C肽反应。