Svartberg J, Holst J J, Gutniak M, Adner N
Karolinska Institute, Department of Internal Medicine, Södersjukhuset, Stockholm, Sweden.
Pancreas. 1998 Jan;16(1):66-71. doi: 10.1097/00006676-199801000-00011.
We studied the effect of ethanol and calcium antagonism (nifedipine) on insulin- (n = 8) and glucagon-like peptide-1 (GLP-1) (n = 6) secretion in healthy subjects. Four experiments in random order were performed (control, ethanol, nifedipine, and combination). Intravenous glucose tolerance tests were performed with and without pretreatment with oral ethanol and nifedipine. Ethanol pretreatment was followed by increased insulin (ethanol vs. control; p < 0.01) and C-peptide (ethanol vs. control; p < 0.05) areas after intravenous glucose (0-20 min), indicating that ethanol augments insulin secretion. Calcium antagonism with nifedipine abolished the ethanol augmentation of insulin secretion (insulin area 0-20 min, ethanol vs. combination, p < 0.05; and C-peptide area 0-20 min, ethanol vs. combination, p < 0.01). The GLP-1 response (area 0-90 min) was not significantly affected by ethanol.
我们研究了乙醇和钙拮抗作用(硝苯地平)对健康受试者胰岛素(n = 8)和胰高血糖素样肽-1(GLP-1)(n = 6)分泌的影响。按随机顺序进行了四项实验(对照、乙醇、硝苯地平及联合用药)。在口服乙醇和硝苯地平预处理前后分别进行静脉葡萄糖耐量试验。乙醇预处理后,静脉注射葡萄糖后0至20分钟的胰岛素(乙醇组与对照组相比;p < 0.01)和C肽(乙醇组与对照组相比;p < 0.05)曲线下面积增加,表明乙醇可增强胰岛素分泌。硝苯地平的钙拮抗作用消除了乙醇对胰岛素分泌的增强作用(胰岛素0至20分钟曲线下面积,乙醇组与联合用药组相比,p < 0.05;C肽0至20分钟曲线下面积,乙醇组与联合用药组相比,p < 0.01)。乙醇对GLP-1反应(0至90分钟曲线下面积)无显著影响。