Hildebrandt W, Brömme H J, Kohnert K D, Blech W
Institut für Biochemie, Bereich Medizin, Martin-Luther-Universität Halle-Wittenberg DDR.
Biomed Biochim Acta. 1989;48(4):211-9.
Hepatic glucagon degradation was studied using recycling perfused livers from 24h fasted rats in the absence of glucose. In comparison with normoxic conditions, a significantly reduced glucagon cleavage was observed within the first 30 min of hypoxic perfusion (acute energy deficiency). On the contrary, glucagon degradation was markedly increased after 30 min. At the same time, increased release of intracellular glucagon-degrading activity occurred. Partial characterization of the degrading activity showed high specificity for glucagon. Both its metal- and thiol-dependent activity and immunological reaction against specific antibodies are characteristic of the insulin-glucagon-proteinase (IGP) of rat liver. These results indicate that a substantial part of the liver-bound glucagon is internalized via an energy-dependent step followed by degradation by IGP.
在无葡萄糖条件下,使用来自禁食24小时大鼠的循环灌注肝脏研究肝胰高血糖素降解。与常氧条件相比,在低氧灌注的最初30分钟内(急性能量缺乏)观察到胰高血糖素裂解显著减少。相反,30分钟后胰高血糖素降解明显增加。同时,细胞内胰高血糖素降解活性的释放增加。对降解活性的部分表征显示对胰高血糖素具有高特异性。其金属依赖性和硫醇依赖性活性以及针对特异性抗体的免疫反应都是大鼠肝脏胰岛素-胰高血糖素-蛋白酶(IGP)的特征。这些结果表明,肝脏结合的胰高血糖素的很大一部分通过能量依赖步骤内化,随后被IGP降解。