Polonsky K S, Given B D, Hirsch L J, Tillil H, Shapiro E T, Beebe C, Frank B H, Galloway J A, Van Cauter E
Department of Medicine, University of Chicago, Pritzker School of Medicine, IL 60637.
N Engl J Med. 1988 May 12;318(19):1231-9. doi: 10.1056/NEJM198805123181903.
To determine whether non-insulin-dependent diabetes is associated with specific alterations in the pattern of insulin secretion, we studied 16 patients with untreated diabetes and 14 matched controls. The rates of insulin secretion were calculated from measurements of peripheral C-peptide in blood samples taken at 15- to 20-minute intervals during a 24-hour period in which the subjects ate three mixed meals. Incremental responses of insulin secretion to meals were significantly lower in the diabetic patients (P less than 0.005), and the increases and decreases in insulin secretion after meals were more sluggish. These disruptions in secretory response were more marked after dinner than after breakfast, and a clear secretory response to dinner often could not be identified. Both the control and diabetic subjects secreted insulin in a series of discrete pulses. In the controls, a total of seven to eight pulses were identified in the period from 9 a.m. to 11 p.m., including the three post-meal periods (an average frequency of one pulse per 105 to 120 minutes), and two to four pulses were identified in the remaining 10 hours. The number of pulses in the patients and controls did not differ significantly. However, in the patients, the pulses after meals had a smaller amplitude (P less than 0.03) and were less frequently concomitant with a glucose pulse (54.7 +/- 4.9 vs. 82.2 +/- 5.0, P less than 0.001). Pulses also appeared less regularly in the patients. During glucose clamping to produce hyperglycemia (glucose level, 16.7 mmol per liter [300 mg per deciliter]), the diabetic subjects secreted, on the average, 70 percent less insulin than matched controls (P less than 0.001). These data suggest that profound alterations in the amount and temporal organization of stimulated insulin secretion may be important in the pathophysiology of beta-cell dysfunction in diabetes.
为了确定非胰岛素依赖型糖尿病是否与胰岛素分泌模式的特定改变相关,我们研究了16例未经治疗的糖尿病患者和14例匹配的对照者。胰岛素分泌率是根据在24小时内每隔15至20分钟采集的血样中外周C肽的测量值计算得出的,在此期间受试者进食三餐混合食物。糖尿病患者餐后胰岛素分泌的增量反应显著降低(P<0.005),餐后胰岛素分泌的增减更为迟缓。晚餐后分泌反应的这些紊乱比早餐后更明显,且常常无法识别对晚餐的明确分泌反应。对照组和糖尿病组受试者均以一系列离散脉冲形式分泌胰岛素。在对照组中,上午9点至晚上11点期间共识别出7至8个脉冲,包括三个餐后时段(平均频率为每105至120分钟一个脉冲),其余10小时内识别出2至4个脉冲。患者和对照组的脉冲数量无显著差异。然而,在患者中,餐后脉冲的幅度较小(P<0.03),且与血糖脉冲同时出现的频率较低(54.7±4.9对82.2±5.0,P<0.001)。患者的脉冲出现也不太规律。在进行葡萄糖钳夹以产生高血糖(血糖水平为16.7 mmol/L[300 mg/dl])时,糖尿病受试者分泌的胰岛素平均比匹配的对照组少70%(P<0.001)。这些数据表明,刺激胰岛素分泌的量和时间组织的深刻改变可能在糖尿病β细胞功能障碍的病理生理学中起重要作用。