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Effect of hepatic glucose production on acute insulin resistance induced by lipid-infusion in awake rats

机译:肝葡萄糖生成对清醒大鼠脂质输注诱导的急性胰岛素抵抗的影响

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摘要

AIM: To explore the influence of hepatic glucose production on acute insulin resistance induced by a lipid infusion in awake rats.METHODS: A hyperinsulinaemic-euglycaemic clamp was established in awake chronically catheterized rats. Two groups of rats were studied either with a 4-h intraarterial infusion of lipid/heparin or saline. Insulin-mediated peripheral and hepatic glucose metabolism was assessed by hyperinsulinaemic-euglycaemic clamp combined with [3-3H]-glucose infusion.RESULTS: During hyperinsulinaemic-euglycaemic clamp, there was a significant increase in plasma free fatty acid (FFA, from 741.9 ± 50.6 to 2346.4 ± 238.5 μmol/L, P < 0.01) in lipid-infused group. The glucose infusion rates (GIR) in the lipid infusion rats, compared to control rats, were significantly reduced (200-240 min average: Lipid infusion; 12.6 ± 1.5 vs control; 34.0 ± 1.6 mg/kg.min, P < 0.01), declining to - 35% of the corresponding control values during the last time of the clamp (240 min: Lipid infusion; 12.0 ± 1.9 vs control; 34.7 ± 1.7 mg/kg·min, P < 0.0001). At the end of clamp study, the hepatic glucose production (HGP) in control rats was significantly suppressed (88%) from 19.0 ± 4.5 (basal) to 2.3 ± 0.9 mg/kg.min (P < 0.01). The suppressive effect of insulin on HGP was significantly blunted in the lipid-infused rats (200-240 min: From 18.7 ± 3.0 to 23.2 ± 3.1 mg/kg·min (P < 0.05). The rate of glucose disappearance (GRd) was a slight decrease in the lipid-infused rats compared with controls during the clamp.CONCLUSION: These data suggest that lipid infusion could induces suppression of hepatic glucose production, impairs the abilities of insulin to suppress lipolysis and mediate glucose utilization in peripheral tissue. Therefore, we conclude that lipid-infusion induces an acute insulin resistance in vivo.
机译:目的:探讨清醒大鼠肝脏葡萄糖生成对脂质输注诱导的急性胰岛素抵抗的影响。方法:在清醒的慢性导管大鼠中建立高胰岛素血症,正常血糖钳位。研究了两组大鼠的脂质/肝素或盐水的4小时动脉内输注。高胰岛素血症-正常血糖钳夹结合[3- 3 H]-葡萄糖输注评估胰岛素介导的外周和肝葡萄糖代谢。结果:在高胰岛素血症-正常血糖钳夹期间,血浆游离水平显着增加脂质注入组中的脂肪酸(FFA,从741.9±50.6到2346.4±238.5μmol/ L,P <0.01)。与对照组相比,脂质输注大鼠的葡萄糖输注速率(GIR)显着降低(平均200-240分钟:脂质输注;与对照组相比为12.6±1.5; 34.0±1.6 mg / kg.min,P <0.01) ,在最后一次钳夹期间下降至相应对照值的-35%(240分钟:脂质输注;相对于对照为12.0±1.9; 34.7±1.7 mg / kg·min,P <0.0001)。在钳夹研究结束时,对照大鼠的肝葡萄糖生成(HGP)从19.0±4.5(基础)显着抑制(88%)至2.3±0.9 mg / kg.min(P <0.01)。在注射脂质的大鼠中,胰岛素对HGP的抑制作用明显减弱(200-240分钟:从18.7±3.0到23.2±3.1 mg / kg·min(P <0.05)),葡萄糖消失率(GRd)为结论:在钳夹期间,与对照组相比,输注脂质的大鼠略有减少。结论:这些数据表明,输注脂质可能会抑制肝葡萄糖的产生,削弱胰岛素抑制脂解和介导周围组织葡萄糖利用的能力。我们得出的结论是,脂质输注在体内可引起急性胰岛素抵抗。

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