Taylor R, Heine R J, Collins J, James O F, Alberti K G
Hepatology. 1985 Jan-Feb;5(1):64-71. doi: 10.1002/hep.1840050115.
In vivo insulin sensitivity and adipocyte insulin binding and action were assessed in 16 patients with histologically proven hepatic cirrhosis and 11 age-, weight- and sex-matched normal control subjects. The cirrhotic group displayed impaired oral glucose tolerance, despite an exaggerated serum immunoreactive insulin response, and in vivo insulin resistance as assessed both by the euglycemic hyperinsulinemic clamp and the glucose-insulin infusion techniques. Adipocytes of the cirrhotic patients bound significantly less insulin than those of the control subjects (2.21 +/- 0.12% vs. 2.64 +/- 0.13%; p less than 0.05). Although the adipocytes from the cirrhotic patients were less sensitive to insulin stimulation in vitro (half-maximal stimulation at 60.0 +/- 8.0 vs. 21.8 +/- 3.3 pM; p less than 0.001), they exhibited higher maximum rates of lipogenesis. Comparison of the responses of the alcoholic, primary biliary cirrhosis and cryptogenic subgroups suggested pronounced differences in the maximum rates of lipogenesis. There were significant negative correlations between specific binding to adipocytes and both fasting serum immunoreactive insulin and in vivo insulin resistance as assessed by glucose-insulin infusion. Monocyte insulin binding was normal in the cirrhotic group and did not correlate with in vivo insulin resistance. It is concluded that both binding and postbinding defects in insulin target organ cells contribute to the marked in vivo insulin resistance of hepatic cirrhosis.
对16例经组织学证实的肝硬化患者和11例年龄、体重及性别相匹配的正常对照者进行了体内胰岛素敏感性、脂肪细胞胰岛素结合及作用的评估。尽管肝硬化组血清免疫反应性胰岛素反应增强,但口服葡萄糖耐量仍受损,通过正常血糖高胰岛素钳夹技术和葡萄糖-胰岛素输注技术评估,其存在体内胰岛素抵抗。肝硬化患者的脂肪细胞结合胰岛素的能力明显低于对照组(2.21±0.12%对2.64±0.13%;p<0.05)。虽然肝硬化患者的脂肪细胞在体外对胰岛素刺激的敏感性较低(半数最大刺激浓度为60.0±8.0对21.8±3.3 pM;p<0.001),但其脂肪生成的最大速率较高。酒精性、原发性胆汁性肝硬化和隐源性亚组的反应比较表明,脂肪生成的最大速率存在明显差异。脂肪细胞特异性结合与空腹血清免疫反应性胰岛素以及通过葡萄糖-胰岛素输注评估的体内胰岛素抵抗之间存在显著负相关。肝硬化组单核细胞胰岛素结合正常,且与体内胰岛素抵抗无关。结论是胰岛素靶器官细胞的结合缺陷和结合后缺陷均导致了肝硬化明显的体内胰岛素抵抗。