Jacquez J A
Am J Physiol. 1992 Jun;262(6 Pt 1):E779-90. doi: 10.1152/ajpendo.1992.262.6.E779.
I present a review and synthesis of the basic theory, steady state, and non-steady state for the calculation of metabolite production rates for systems that have a central well-mixed compartment that is the site of tracer input and sampling. The theory is then applied to the calculation of glucose production. If the only inputs are into the central compartment, an experimental design that involves varying tracer infusion rates to maintain constant specific activity in the central compartment and the same constant specific activity in the peripheral compartments allows calculation of the endogenous production. That holds even if the models are unidentifiable. The correct equation and Steele's pool fraction approximation reduce to the same result for this experimental design. However, that does not justify the use of Steele's equation when there are deviations from the exact experimental design. When the specific activity in the central compartment is not constant, model-dependent correction terms to Steele's equation are needed.
我对具有一个中央充分混合隔室(即示踪剂输入和采样位点)的系统中代谢物生成速率计算的基本理论、稳态和非稳态进行了综述与综合。然后将该理论应用于葡萄糖生成的计算。如果唯一的输入进入中央隔室,一种实验设计是通过改变示踪剂输注速率,以维持中央隔室内特定活性恒定,同时外周隔室内特定活性保持相同的恒定值,这样就可以计算内源性生成。即使模型不可识别,这一方法依然成立。对于该实验设计,正确的方程和斯蒂尔的池分数近似法会得出相同的结果。然而,当与精确的实验设计存在偏差时,这并不足以证明可以使用斯蒂尔方程。当中央隔室内的特定活性不恒定时,就需要对斯蒂尔方程使用依赖模型的校正项。