Goresky C A, Bach G G, Schwab A J
McGill University Medical Clinic, Montreal General Hospital, Quebec, Canada.
Am J Physiol. 1993 Jun;264(6 Pt 2):H2007-28. doi: 10.1152/ajpheart.1993.264.6.H2007.
Distributed-in-space conversion of precursor substrate to product within an organ is explored when all formed product is released into the bloodstream. When precursor removal kinetics are linear (conversion occurring proportionately to concentration) and the process is uniformly distributed along the length, exponentially decreasing concentration profiles for precursor result. The vascular profile for product rises in complementary fashion; the sum of precursor and product is constant along the length. Symmetric permeability barriers are found to produce concentration stepdowns of precursor from blood to tissue and, for product, converse stepdowns from tissue to blood. Tracer precursor, introduced as an impulse input, within this steady state, is converted to product, details varying with the number of barriers. Nevertheless, a particular common feature is found in the solutions. The analytic expression for locally generated tracer product is found, in each case, to contain the impulse response to tracer product introduced at the origin. Therefore, to simplify experimental analysis and to superpose a set of constraints on computational approaches to parameter estimation, one should introduce, simultaneously with tracer precursor, tracer product labeled in an identifiably different manner.
当所有生成的产物释放到血液中时,我们探讨了器官内前体底物到产物在空间上的分布式转化。当前体去除动力学呈线性(转化与浓度成比例发生)且过程沿长度均匀分布时,前体的浓度分布呈指数下降。产物的血管分布以互补方式上升;前体和产物的总和沿长度恒定。发现对称的渗透屏障会导致前体从血液到组织的浓度下降,而对于产物,则是从组织到血液的相反下降。在这种稳态下,作为脉冲输入引入的示踪前体被转化为产物,具体细节随屏障数量而变化。然而,在这些解中发现了一个特别共同的特征。在每种情况下,发现局部生成的示踪产物的解析表达式都包含对在原点引入的示踪产物的脉冲响应。因此,为了简化实验分析并对参数估计的计算方法施加一组约束,应该在前体示踪剂引入的同时,引入以可识别的不同方式标记的产物示踪剂。