Dow R J, Baty J, Isles T E
Br J Clin Pharmacol. 1985;20 Suppl 1(Suppl 1):75S-83S. doi: 10.1111/j.1365-2125.1985.tb05146.x.
The effect of nicardipine on insulin secretion was examined in two double-blind, randomised, cross-over, placebo-controlled studies in normal volunteers. In the first study, the effect of acute dosing (via an intravenous infusion of 5 mg h-1 for 3 h) on the glucose, insulin, hormonal, and intermediary metabolite responses to an intravenous glucose tolerance test was determined in six healthy male volunteers. In the second study, the glucose, insulin, and C-peptide responses to intravenous tolbutamide (200 mg) was determined in another six male volunteers after oral dosing with nicardipine 30 mg three times daily for 1 week. A relative increase in insulin secretion was the principal finding of the first study. No other response was affected significantly. No significant differences between the nicardipine- and placebo-treated groups were noted in the insulin, glucose, and C-peptide measurements of the second study. In conclusion, treatment with nicardipine does not appear to impair insulin secretion in response either to an intravenous glucose load or intravenously administered tolbutamide.
在两项针对正常志愿者的双盲、随机、交叉、安慰剂对照研究中,检测了尼卡地平对胰岛素分泌的影响。在第一项研究中,测定了6名健康男性志愿者静脉输注5mg/h共3小时急性给药后,对静脉葡萄糖耐量试验的葡萄糖、胰岛素、激素及中间代谢产物反应的影响。在第二项研究中,另6名男性志愿者每日3次口服30mg尼卡地平,持续1周后,测定静脉注射甲苯磺丁脲(200mg)后的葡萄糖、胰岛素及C肽反应。第一项研究的主要发现是胰岛素分泌相对增加。无其他反应受到显著影响。第二项研究中,尼卡地平治疗组与安慰剂治疗组在胰岛素、葡萄糖及C肽测量方面无显著差异。总之,尼卡地平治疗似乎不会损害对静脉葡萄糖负荷或静脉注射甲苯磺丁脲的胰岛素分泌反应。