Shamoon H, Baylor P, Kambosos D, Charlap S, Plawes S, Frishman W H
J Clin Endocrinol Metab. 1985 Mar;60(3):536-41. doi: 10.1210/jcem-60-3-536.
We evaluated the effect of treatment with placebo or verapamil (320 mg/day) for 2 weeks on glucose-induced insulin secretion and hypoglycemia-stimulated counterregulatory hormone secretion in hypertensive patients. Verapamil treatment was associated with a significant reduction in diastolic blood pressure (P = 0.02 vs. placebo). During a hyperglycemic clamp (plasma glucose raised 125 mg/dl above basal level) maintained for 90 min, plasma insulin increased 4- to 5-fold (early) and then to values 8- to 10-fold above baseline (late). These increments were identical during placebo or verapamil treatment. The rates of glucose metabolized during each study also were similar, suggesting that no significant change in insulin action occurred during drug treatment. When plasma glucose was allowed to decline precipitously from hyperglycemic levels (220 mg/dl) to nadirs ranging from 42-77 mg/dl, plasma concentrations of glucagon, cortisol, epinephrine, and norepinephrine all increased; however, no consistent differences in the counter-regulatory hormone responses could be attributed to verapamil therapy. We conclude that physiologically effective drug concentrations of verapamil capable of influencing blood pressure do not have a significant effect on secretion of glucoregulatory hormones in man.
我们评估了安慰剂或维拉帕米(320毫克/天)治疗2周对高血压患者葡萄糖诱导的胰岛素分泌和低血糖刺激的反调节激素分泌的影响。维拉帕米治疗与舒张压显著降低相关(与安慰剂相比,P = 0.02)。在维持90分钟的高血糖钳夹期间(血浆葡萄糖比基础水平升高125毫克/分升),血浆胰岛素早期增加4至5倍,然后增加至基线以上8至10倍(后期)。在安慰剂或维拉帕米治疗期间,这些增加是相同的。每项研究期间葡萄糖代谢率也相似,表明药物治疗期间胰岛素作用未发生显著变化。当血浆葡萄糖从高血糖水平(220毫克/分升)急剧下降至42 - 77毫克/分升的最低点时,胰高血糖素、皮质醇、肾上腺素和去甲肾上腺素的血浆浓度均升高;然而,反调节激素反应中没有一致的差异可归因于维拉帕米治疗。我们得出结论,能够影响血压的生理有效浓度的维拉帕米对人体葡萄糖调节激素的分泌没有显著影响。