[3-13C]丙酮酸在大鼠肝细胞中生成d-葡萄糖的不对称标记

I. Verbruggen , L. Ladrière , R. Willem , W.J. Malaisse
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引用次数: 6

摘要

大鼠肝细胞在10 mm[3-13C]丙酮酸存在下孵育30或120分钟,用13c NMR评估13c标记的葡萄糖同位素体的生成。c1标记葡萄糖的量超过了c2标记己糖的量,而c2标记己糖的量又高于c3标记葡萄糖的量。在己糖的c6 - c5 - c4部分中观察到类似的层次结构。然而,葡萄糖的后一部分比c3 - c2 - c1部分更有效地被标记。这一发现与先前报道的和本研究中肝细胞暴露于[2-13C]丙酮酸时再次观察到的结果相似。因此,这些趋同的观察结果支持了3-磷酸甘油醛在3-磷酸甘油醛脱氢酶和磷酸果糖醛缩酶之间的酶对酶通道的概念。
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Asymmetrical Labeling ofd-Glucose Generated from [3-13C]Pyruvate in Rat Hepatocytes

The generation of13C-labeledd-glucose isotopomers by rat hepatocytes incubated for 30 or 120 min in the presence of 10 mm[3-13C]pyruvate was assessed by13C NMR. The amount of C1-labeledd-glucose exceeded that of C2-labeled hexose, which was itself higher than that of C3-labeledd-glucose. A comparable hierarchy was observed in the C6–C5–C4moiety of the hexose. The latter moiety ofd-glucose was more efficiently labeled, however, than the C3–C2–C1moiety. This finding is similar to that both previously reported and again observed in the present study when hepatocytes were exposed to [2-13C]pyruvate. These converging observations thus support the concept of enzyme-to-enzyme channeling ofd-glyceraldehyde 3-phosphate between glyceraldehyde-3-phosphate dehydrogenase and phosphofructoaldolase.

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