Kraegen E W, Chisholm D J, Hewett M J
Diabetes Care. 1983 Mar-Apr;6(2):118-21. doi: 10.2337/diacare.6.2.118.
Continuous insulin infusion via the subcutaneous (s.c.) route is attractive for diabetes therapy because of its simplicity compared with other routes. Some insulin will be degraded locally before systemic absorption, although the magnitude of this degradation has not been established. We have performed in five normal subjects s.c. and intravenous (i.v.) insulin infusions (2.4 U/h) of sufficient duration to compare steady-state systemic appearance rates of exogenous insulin. A steady state was produced after 60-90 min (i.v.) and 6-8 h (s.c.). Blood glucose fell to approximately 2.7 mmol/L in both studies and a fall in C-peptide indicated suppression of endogenous insulin secretion. Plateau insulin levels attributable to systemic entry of exogenous insulin were 36 +/- 2.0 mU/L (i.v. route) and 29 +/- 1.8 mU/L (s.c. route). These indicate a rate of 2.c. degradation of insulin of 19 +/- 5% in the steady state. We conclude that there is a low rate of degradation of insulin during continuous s.c. infusion.
与其他给药途径相比,皮下持续输注胰岛素治疗糖尿病具有简便的优势。尽管尚未明确胰岛素在皮下局部降解的程度,但部分胰岛素会在全身吸收之前发生局部降解。我们对5名正常受试者进行了皮下和静脉胰岛素输注(2.4 U/h),输注时间足够长,以比较外源性胰岛素的稳态全身出现率。静脉输注60 - 90分钟和皮下输注6 - 8小时后达到稳态。两项研究中血糖均降至约2.7 mmol/L,C肽下降表明内源性胰岛素分泌受到抑制。外源性胰岛素全身进入导致的胰岛素平台水平在静脉输注途径为36±2.0 mU/L,皮下输注途径为29±1.8 mU/L。这些结果表明,稳态下胰岛素的皮下降解率为19±5%。我们得出结论,皮下持续输注期间胰岛素的降解率较低。