Arora K K, Smith R, Williams J F
Int J Biochem. 1987;19(2):147-58. doi: 10.1016/0020-711x(87)90325-9.
The phenomenon of "pyruvate recycling" is demonstrated in perfused rat liver, rabbit liver in situ and in Morris Hepatoma 5123TC cells and quantitatively measured using [2-14C]pyruvate and the method of Friedmann et al. (1971). Various metabolites, viz. lactate, DHAP, glucose, glucose 6-P and fructose 6-P were isolated and degraded following the metabolism of [2-14C]pyruvate and [2-14C]glycerol in order to assess the 14C-distributions imparted by "pyruvate recycling" reactions. The labelling of DHAP, lactate, glucose and glucose 6-P showed 14C randomizations consistent with the operation and the quantitative extent of "pyruvate recycling". These findings support the proposal that the actions of "pyruvate recycling" may account for the failure to find significant levels of 14C isotope at C-1 of glucose 6-P following the metabolism of [4,5,6-14C]- or [6-14C]glucose by L-type pentose pathway metabolism in aerobic intact tissues. "Pyruvate recycling" diminishes the measured value of the L-type pentose cycle in intact tissues and qualifies one of the mechanistic predictions of the L-type pentose pathway which was unravelled by tracing its reactions with labelled ribose 5-P and liver enzymes (Horecker et al., 1954; Williams et al., 1978a,b) in vitro. The demonstration of an association of L-type pentose pathway reactions with "pyruvate recycling" by way of the common reactions of their triose-P intermediates qualifies the superficial acceptance of the predictions of the L-type pathway in vitro for the distribution of isotopic labels by aerobic tissues in vivo.
在灌注大鼠肝脏、原位兔肝脏以及莫里斯肝癌5123TC细胞中证实了“丙酮酸循环”现象,并使用[2-¹⁴C]丙酮酸及Friedmann等人(1971年)的方法进行了定量测定。在[2-¹⁴C]丙酮酸和[2-¹⁴C]甘油代谢后,分离并降解了各种代谢物,即乳酸、磷酸二羟丙酮、葡萄糖、葡萄糖6-磷酸和果糖6-磷酸,以评估“丙酮酸循环”反应赋予的¹⁴C分布。磷酸二羟丙酮、乳酸、葡萄糖和葡萄糖6-磷酸的标记显示¹⁴C随机化,与“丙酮酸循环”的运行及定量程度一致。这些发现支持了以下观点:在有氧完整组织中,通过L型戊糖途径代谢[4,5,6-¹⁴C]-或[6-¹⁴C]葡萄糖后,在葡萄糖6-磷酸的C-1位未发现显著水平的¹⁴C同位素,可能是“丙酮酸循环”作用的结果。“丙酮酸循环”降低了完整组织中L型戊糖循环的测量值,并对L型戊糖途径的一个机制预测进行了修正,该预测是通过在体外追踪其与标记核糖5-磷酸和肝脏酶的反应而揭示的(Horecker等人,1954年;Williams等人,1978a,b)。通过其磷酸丙糖中间体的共同反应证明L型戊糖途径反应与“丙酮酸循环”相关,这修正了体外对L型途径预测的表面接受,即关于有氧组织在体内同位素标记分布的预测。