Uete T, Shimano N, Shimizu S, Morikawa M
Metabolism. 1976 Apr;25(4):375-84. doi: 10.1016/0026-0495(76)90069-x.
An autoregulatory system of insulin degradation in the liver in which the rate of insulin metabolism changes in response to fluctuation in its blood levels, was investigated. In the plasma of rats and man in the absence of reduced glutathione (GSH), insulin degradation was not observed, but when a sufficient amount of reduced glutathione was added, the plasma did degrade insulin. This GSH-dependent insulin degrading activity in plasma was quite similar to that in liver in its nature. In rats, this GSH-dependent insulin degrading activity in the liver and plasma was fluctuated in response to fluctuation in the blood insulin levels, and the GSH-dependent insulin degrading activity in plasma was well correlated with that in the liver. Similarly, in man the GSH-dependent insulin degrading activity in plasma was changed in response to fluctuation in the blood insulin levels. In plasma under the physiologic conditions, there is an insufficient amount of reduced glutathione to elicit the insulin degrading activity, but in the liver there is a sufficient amount of reduced glutathione to manifest this activity. This evidence further supports the concept that an autoregulatory system of insulin degradation in the liver exists in man.
对肝脏中胰岛素降解的一种自动调节系统进行了研究,在该系统中,胰岛素代谢速率会随着其血液水平的波动而变化。在大鼠和人的血浆中,若不存在还原型谷胱甘肽(GSH),则未观察到胰岛素降解,但当添加足量的还原型谷胱甘肽时,血浆确实会降解胰岛素。血浆中这种依赖GSH的胰岛素降解活性在本质上与肝脏中的非常相似。在大鼠中,肝脏和血浆中这种依赖GSH的胰岛素降解活性会随着血液胰岛素水平的波动而波动,且血浆中依赖GSH的胰岛素降解活性与肝脏中的密切相关。同样,在人类中,血浆中依赖GSH的胰岛素降解活性也会随着血液胰岛素水平的波动而变化。在生理条件下的血浆中,还原型谷胱甘肽的量不足以引发胰岛素降解活性,但在肝脏中有足量的还原型谷胱甘肽来表现这种活性。这一证据进一步支持了人类肝脏中存在胰岛素降解自动调节系统这一概念。