Katz H, Homan M, Jensen M, Caumo A, Cobelli C, Rizza R
Department of Medicine, Mayo Clinic, Rochester, Minnesota 55905.
Diabetes. 1994 Feb;43(2):289-96. doi: 10.2337/diab.43.2.289.
Both glucose and insulin are important regulators of glucose uptake and hepatic glucose release. Because insulin concentrations rarely if ever increase under daily living conditions, unless glucose concentrations also increase, we sought to determine whether hepatic and extrahepatic responses to changes in insulin and glucose concentration are impaired in patients with non-insulin-dependent diabetes mellitus (NIDDM). To address this question, glucose metabolism was measured in diabetic and nondiabetic subjects. A computer-driven infusion system was used to produce a nondiabetic postprandial insulin profile in both groups while sufficient exogenous glucose was infused to mimic nondiabetic postprandial glucose concentrations. Although NIDDM was associated with greater (P < 0.05) hepatic glucose release both before and during the prandial insulin infusion, suppression did not differ in the diabetic and nondiabetic subjects (-1.06 +/- 0.20 vs. -0.86 +/- 0.15 mmol/kg every 4 h). In contrast, stimulation of both glucose disappearance (0.77 +/- 0.27 vs. 1.68 +/- 0.27 mmol/kg every 4 h) and forearm glucose uptake (187 +/- 81 vs. 550 +/- 149 mumol/dl every 4 h) was lower (P < 0.05) in diabetic than in nondiabetic subjects. Thus, despite increased basal rates of glucose production, obese individuals with NIDDM had decreased stimulation of glucose disappearance but normal suppression of hepatic glucose release in response to nondiabetic prandial glucose and insulin concentrations. These data indicate that the increase in glucose that occurs with carbohydrate ingestion is likely to compensate for hepatic but not extrahepatic insulin resistance.
葡萄糖和胰岛素都是葡萄糖摄取及肝脏葡萄糖释放的重要调节因子。因为在日常生活条件下,除非葡萄糖浓度也升高,胰岛素浓度极少会升高,所以我们试图确定非胰岛素依赖型糖尿病(NIDDM)患者肝脏和肝外组织对胰岛素及葡萄糖浓度变化的反应是否受损。为解决这个问题,我们对糖尿病患者和非糖尿病患者的葡萄糖代谢情况进行了测量。使用计算机驱动的输注系统,在两组患者中模拟非糖尿病餐后胰岛素水平,同时输注足够的外源性葡萄糖以模拟非糖尿病餐后葡萄糖浓度。虽然在餐时胰岛素输注前及输注过程中,NIDDM患者的肝脏葡萄糖释放均较多(P<0.05),但糖尿病患者和非糖尿病患者肝脏葡萄糖释放的抑制程度并无差异(每4小时分别为-1.06±0.20与-0.86±0.15 mmol/kg)。相比之下,糖尿病患者的葡萄糖消失刺激(每4小时分别为0.77±0.27与1.68±0.27 mmol/kg)和前臂葡萄糖摄取(每4小时分别为187±81与550±149 μmol/dl)均低于非糖尿病患者(P<0.05)。因此,尽管基础葡萄糖生成率升高,但伴有NIDDM的肥胖个体在面对非糖尿病餐时葡萄糖和胰岛素浓度时,葡萄糖消失刺激降低,但肝脏葡萄糖释放抑制正常。这些数据表明,碳水化合物摄入后出现的葡萄糖升高可能会补偿肝脏而非肝外组织的胰岛素抵抗。