Duckworth W C, Gifford D, Kitabchi A E, Runyan K, Solomon S S
Diabetes. 1979 Aug;28(8):746-8. doi: 10.2337/diab.28.8.746.
Insulin degradtion by muscle was examined in normal, streptozotocin-induced diabetic rats, and diabetic rats treated with insulin. Insulin degradation by the 100,000 X g supernatant fractions was identical in all three groups, but insulin metabolism by the intact epitrochlaris muscle was significantly increased in diabetic animals. Insulin treatment of the diabetic animals partially restored the activity toward normal. Specific binding of 125l-insulin to the intact muscles was also increased in the diabetic animals. Streptozotocin diabetes, therefore, increased the binding and degradation of insulin by intact muscle but did not alter the insulin degradation by the total soluble intracellular degradative activity.
在正常大鼠、链脲佐菌素诱导的糖尿病大鼠以及接受胰岛素治疗的糖尿病大鼠中,研究了肌肉对胰岛素的降解情况。三组动物中,100,000×g 上清液组分对胰岛素的降解作用相同,但糖尿病动物完整的肱三头肌对胰岛素的代谢显著增加。对糖尿病动物进行胰岛素治疗可使活性部分恢复至正常水平。糖尿病动物中,125I 胰岛素与完整肌肉的特异性结合也增加。因此,链脲佐菌素诱导的糖尿病增加了完整肌肉对胰岛素的结合和降解,但并未改变总可溶性细胞内降解活性对胰岛素的降解作用。