Misbin R I, Almira E C, Duckworth W C, Mehl T D
Endocrinology. 1983 Oct;113(4):1525-7. doi: 10.1210/endo-113-4-1525.
The effect of insulin-like growth factors (IGF 1 and IGF 2) on insulin degradation was studied with the use of a preparation of insulin protease from rat skeletal muscle. Insulin, IGF 1 and IGF 2 inhibited 125I-insulin degradation by this enzyme. IGF 2 was the most potent inhibitor and IGF 1 was the least potent. These results are similar to what has been reported previously for the insulin-degrading activity in the serum of a diabetic patient who was resistant to sc and im insulin. Insulin protease also degraded 125I-iodo IGF 1 and 125I-iodo IGF 2. 125I-iodo IGF 2 was degraded more rapidly than was 125I-iodo IGF 1. 125I-iodoinsulin was degraded more rapidly than 125I-iodo IGF 2. With all three peptides, immunoprecipitation was a more sensitive measure of degradation than was trichloroacetic acid precipitation. The results suggest that insulin protease may be responsible for the degradation of insulin-like growth factors as well as of insulin.
利用大鼠骨骼肌胰岛素蛋白酶制剂研究了胰岛素样生长因子(IGF-1和IGF-2)对胰岛素降解的影响。胰岛素、IGF-1和IGF-2均可抑制该酶对125I-胰岛素的降解。IGF-2是最有效的抑制剂,IGF-1是效力最弱的。这些结果与先前报道的一名对皮下和肌肉注射胰岛素耐药的糖尿病患者血清中胰岛素降解活性的情况相似。胰岛素蛋白酶也可降解125I-碘IGF-1和125I-碘IGF-2。125I-碘IGF-2比125I-碘IGF-1降解得更快。125I-碘胰岛素比125I-碘IGF-2降解得更快。对于所有这三种肽,免疫沉淀法是比三氯乙酸沉淀法更灵敏的降解检测方法。结果表明,胰岛素蛋白酶可能负责胰岛素样生长因子以及胰岛素的降解。