Dirlewanger M, Schneiter P, Jéquier E, Tappy L
Institute of Physiology, University of Lausanne Medical School, 1005 Lausanne, Switzerland.
Am J Physiol Endocrinol Metab. 2000 Oct;279(4):E907-11. doi: 10.1152/ajpendo.2000.279.4.E907.
Hepatic and extrahepatic insulin sensitivity was assessed in six healthy humans from the insulin infusion required to maintain an 8 mmol/l glucose concentration during hyperglycemic pancreatic clamp with or without infusion of 16.7 micromol. kg(-1). min(-1) fructose. Glucose rate of disappearance (GR(d)), net endogenous glucose production (NEGP), total glucose output (TGO), and glucose cycling (GC) were measured with [6,6-(2)H(2)]- and [2-(2)H(1)]glucose. Hepatic glycogen synthesis was estimated from uridine diphosphoglucose (UDPG) kinetics as assessed with [1-(13)C]galactose and acetaminophen. Fructose infusion increased insulin requirements 2.3-fold to maintain blood glucose. Fructose infusion doubled UDPG turnover, but there was no effect on TGO, GC, NEGP, or GR(d) under hyperglycemic pancreatic clamp protocol conditions. When insulin concentrations were matched during a second hyperglycemic pancreatic clamp protocol, fructose administration was associated with an 11.1 micromol. kg(-1). min(-1) increase in TGO, a 7.8 micromol. kg(-1). min(-1) increase in NEGP, a 2.2 micromol. kg(-1). min(-1) increase in GC, and a 7.2 micromol. kg(-1). min(-1) decrease in GR(d) (P < 0. 05). These results indicate that fructose infusion induces hepatic and extrahepatic insulin resistance in humans.
在六名健康人体中评估了肝内和肝外胰岛素敏感性,评估方法是在高血糖胰腺钳夹期间,在输注或不输注16.7微摩尔·千克⁻¹·分钟⁻¹果糖的情况下,根据维持8毫摩尔/升血糖浓度所需的胰岛素输注量来进行。使用[6,6-(²)H₂]-和[2-(²)H₁]葡萄糖测量葡萄糖消失率(GR(d))、净内源性葡萄糖生成(NEGP)、总葡萄糖输出(TGO)和葡萄糖循环(GC)。通过用[1-(¹³)C]半乳糖和对乙酰氨基酚评估的尿苷二磷酸葡萄糖(UDPG)动力学来估计肝糖原合成。输注果糖使维持血糖所需的胰岛素量增加了2.3倍。在高血糖胰腺钳夹方案条件下,输注果糖使UDPG周转率增加了一倍,但对TGO、GC、NEGP或GR(d)没有影响。当在第二个高血糖胰腺钳夹方案中胰岛素浓度匹配时,给予果糖与TGO增加11.1微摩尔·千克⁻¹·分钟⁻¹、NEGP增加7.8微摩尔·千克⁻¹·分钟⁻¹、GC增加2.2微摩尔·千克⁻¹·分钟⁻¹以及GR(d)降低7.2微摩尔·千克⁻¹·分钟⁻¹相关(P<0.05)。这些结果表明,输注果糖会在人体中诱导肝内和肝外胰岛素抵抗。