Thorsteinsson B, Fugleberg S, Feldt-Rasmussen B, Binder C
Acta Pharmacol Toxicol (Copenh). 1985 Nov;57(5):309-16. doi: 10.1111/j.1600-0773.1985.tb00050.x.
Three theoretical kinetic models for plasma disappearance of insulin were examined in six normal men. The models allowed for the existence of non-saturable and/or saturable mechanisms. Constant infusion of porcine insulin at different rates was used to achieve different levels of steady state plasma insulin concentrations, while normoglycaemia was secured by a glucose clamp technique. Appropriate validation procedures demonstrated that one of the three models was superior to the others in describing the relationship between the exogenous insulin infusion rate Iex and the steady state plasma insulin concentration C: Iex = -Iend + k2 X C/(k3 + C), where Iend is the endogenous post-hepatic insulin delivery rate. Thus, only saturable mechanism(s) could be demonstrated. The median value of k2 (the maximal insulin disappearance rate) and k3 (the plasma insulin concentration at which the insulin disappearance rate is half maximal) were 7.31 nmol X min.-1 and 3.89 nmol X 1-1. The median value of k2/k3 (the clearance rate of insulin for infinitesimal plasma insulin concentrations) was 25.0 ml X kg-1 X min.-1. Thus, at physiological levels of plasma insulin concentrations the metabolic clearance rate of insulin is higher than insulin clearance estimates previously reported in studies based on the assumption of first order kinetics.
在六名正常男性中研究了胰岛素血浆消失的三种理论动力学模型。这些模型考虑了非饱和和/或饱和机制的存在。通过以不同速率持续输注猪胰岛素来达到不同水平的稳态血浆胰岛素浓度,同时通过葡萄糖钳夹技术维持正常血糖水平。适当的验证程序表明,在描述外源性胰岛素输注速率Iex与稳态血浆胰岛素浓度C之间的关系时,三种模型中的一种优于其他模型:Iex = -Iend + k2×C/(k3 + C),其中Iend是肝后内源性胰岛素释放速率。因此,仅能证明存在饱和机制。k2(最大胰岛素消失速率)和k3(胰岛素消失速率为最大值一半时的血浆胰岛素浓度)的中位数分别为7.31 nmol·min-1和3.89 nmol·L-1。k2/k3(无限小血浆胰岛素浓度时胰岛素的清除率)的中位数为25.0 ml·kg-1·min-1。因此,在生理水平的血浆胰岛素浓度下,胰岛素的代谢清除率高于先前基于一级动力学假设的研究所报道的胰岛素清除率估计值。