Brown G C
Department of Biochemistry and Molecular Biology, University College London, U.K.
Biochem J. 1994 Jan 1;297 ( Pt 1)(Pt 1):115-22. doi: 10.1042/bj2970115.
Metabolic control analysis is adapted as a method for describing and analysing the control by organs in the body over the fluxes and concentrations of substances carried in the blood. This physiological control analysis can most usefully be applied to substances with fluxes into and out of organs that are uniquely dependent only on their plasma concentrations. The organ flux of a substance is defined as the steady-state net flux of a substance into a particular organ. The organ flux control coefficients quantify the extent to which a particular organ controls the flux of a substance into the same or another particular organ. Organ concentration control coefficients quantify the extent to which an organ controls the steady-state concentration of a substance in the blood. The control coefficients are additive and obey summation, connectivity and branching theorems. Thus the control coefficients can be determined experimentally by measuring the sensitivities (elasticities) of organ fluxes to the plasma concentration of the substance. As an example of the application of these concepts, the control of ketone-body metabolism in vivo is analysed using data from the literature.
代谢控制分析被用作一种描述和分析身体中各器官对血液中携带物质的通量和浓度进行控制的方法。这种生理控制分析最有效地应用于那些进出器官的通量仅唯一地取决于其血浆浓度的物质。物质的器官通量定义为物质进入特定器官的稳态净通量。器官通量控制系数量化了特定器官对物质进入同一或另一个特定器官的通量的控制程度。器官浓度控制系数量化了器官对血液中物质稳态浓度的控制程度。控制系数具有可加性,并遵循总和、连通性和分支定理。因此,控制系数可以通过测量器官通量对物质血浆浓度的敏感性(弹性)来通过实验确定。作为这些概念应用的一个例子,利用文献数据对体内酮体代谢的控制进行了分析。