Ng C K, Holden J E, DeGrado T R, Raffel D M, Kornguth M L, Gatley S J
Department of Medical Physics, University of Wisconsin, Madison 53706.
Am J Physiol. 1991 Feb;260(2 Pt 2):H593-603. doi: 10.1152/ajpheart.1991.260.2.H593.
The lumped constant (LC) that relates the steady-state phosphorylation rate of 2-[18F]-fluoro-2-deoxy-D-glucose (2-FDG) to that of glucose was determined in an isolated working rat heart model by direct assay of phosphorylation product formation. Five conditions were tested: 5 and 30 mM glucose without insulin, and 2, 3.5, and 5 mM glucose + 10 mU/ml insulin, all at high external work load. Hearts were continuously perfused with 2-FDG and tritiated glucose without recirculation. The steady-state production of tritiated water was used to monitor the glucose phosphorylation rate. Perfused hearts were freeze-clamped and extracted in perchloric acid, and 2-FDG-6-phosphate was separated from 2-FDG with a formate column. The accumulation of 2-FDG phosphorylation products in tissue was also determined from the slopes of the total tissue radioactivity time courses measured by external gamma-ray detection. Without insulin, the LC value decreased 18% as perfusate glucose concentration was increased sixfold (0.94 +/- 0.06 at 5 mM vs. 0.77 +/- 0.17 at 30 mM). With insulin, the LC rose from 0.33 +/- 0.03 at 5 mM to 1.19 +/- 0.05 at 2 mM glucose concentration. The trends can be interpreted in terms of the concept of control strength; the LC value rises as glycolysis becomes rate limited by transport into cells. This potential variability of the LC must be addressed in the quantitative interpretation of myocardial deoxyglucose studies.
通过直接测定磷酸化产物的形成,在离体工作大鼠心脏模型中确定了将2-[¹⁸F]-氟-2-脱氧-D-葡萄糖(2-FDG)的稳态磷酸化速率与葡萄糖的稳态磷酸化速率相关联的集总常数(LC)。测试了五种条件:无胰岛素时的5和30 mM葡萄糖,以及2、3.5和5 mM葡萄糖+ 10 mU/ml胰岛素,均处于高外部工作负荷下。心脏持续灌注2-FDG和氚标记的葡萄糖,不进行再循环。利用氚标记水的稳态产生来监测葡萄糖磷酸化速率。将灌注的心脏冷冻钳夹并在高氯酸中提取,用甲酸盐柱将2-FDG-6-磷酸与2-FDG分离。还通过外部γ射线检测测量的总组织放射性时间进程的斜率来确定组织中2-FDG磷酸化产物的积累。无胰岛素时,随着灌注液葡萄糖浓度增加六倍,LC值降低18%(5 mM时为0.94±0.06,30 mM时为0.77±0.17)。有胰岛素时,LC从5 mM时的0.33±0.03上升至2 mM葡萄糖浓度时的1.19±0.05。这些趋势可以根据控制强度的概念来解释;随着糖酵解因转运进入细胞而成为速率限制因素,LC值升高。在心肌脱氧葡萄糖研究的定量解释中必须考虑LC的这种潜在变异性。