Eaton R P, Allen R C, Schade D S
J Clin Endocrinol Metab. 1983 Jun;56(6):1294-300. doi: 10.1210/jcem-56-6-1294.
The hepatic extraction of insulin in normal man was evaluated by kinetic analysis of peripheral insulin behavior in the plasma following stimulation of endogenous insulin secretion. Prehepatic insulin production was determined by deconvolution of plasma connecting peptide behavior (C-peptide) and hepatic extraction of the secreted insulin determined with a three-compartment model for hepatic, vascular, and extravascular plasma spaces. Three dosages of oral glucose (10, 25, and 100 g) administered to normal volunteers resulted in 1.8 +/- 0.5, 2.7 +/- 1.1, and 7.2 +/- 1.6 U endogenous insulin secretion, respectively. Total hepatic exposure to insulin exceeded the endogenous secretion due to recycling to the liver from the systemic circulation. Decreasing insulin extraction by the liver (67-53-42%) in the presence of increasing insulin exposure (2.6-4.4-13.2 U) was observed during the dose-response to glucose. The rates of hepatic insulin extraction observed with arginine (58 +/- 9% with 3.2 U), and a normal meal (50 +/- 9% with 7.6 U) were intermediate between the extremes seen with the 10- and 100-g glucose challenge. These results quantitate hepatic exposure of insulin in man during differing stimuli of endogenous insulin secretion, and demonstrate reduced fractional hepatic extraction with increasing insulin exposure.
通过对刺激内源性胰岛素分泌后血浆中胰岛素外周行为的动力学分析,评估了正常人体内肝脏对胰岛素的摄取情况。通过对血浆连接肽行为(C肽)进行反卷积来确定肝前胰岛素的产生,并采用肝、血管和血管外血浆空间的三室模型来确定分泌胰岛素的肝脏摄取情况。给正常志愿者服用三种剂量的口服葡萄糖(10克、25克和100克),分别导致内源性胰岛素分泌量为1.8±0.5、2.7±1.1和7.2±1.6单位。由于从体循环再循环至肝脏,肝脏对胰岛素的总暴露量超过了内源性分泌量。在对葡萄糖的剂量反应过程中,观察到随着胰岛素暴露量增加(2.6 - 4.4 - 13.2单位),肝脏对胰岛素的摄取减少(67% - 53% - 42%)。用精氨酸(3.2单位时为58±9%)和正常餐食(7.6单位时为50±9%)观察到的肝脏胰岛素摄取率介于10克和100克葡萄糖激发所观察到的极端值之间。这些结果定量了人体内不同内源性胰岛素分泌刺激期间肝脏对胰岛素的暴露情况,并表明随着胰岛素暴露量增加,肝脏的分数摄取减少。