Nikiforov A A, Ostretsova I B
Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, St Petersburg.
Biochem Pharmacol. 1992 Dec 1;44(11):2213-21. doi: 10.1016/0006-2952(92)90349-n.
Using inhibitors of gluconeogenesis (phenylpyruvate, alpha-cyano-4-hydroxycinnamate, quinolinate, D-malate, aminooxyacetate), we analysed mechanisms by which the gluconeogenic substrates, lactate and pyruvate, as well as a short-chain fatty acid, acetate, stimulate the uptake of a weak organic acid, fluorescein, in the rat kidney. We have shown that these inhibitors modified both the rate of glucose production from lactate and pyruvate in the renal cortex fragment suspension and the stimulatory effects of the metabolic substrates on fluorescein uptake in superficial proximal tubules in the renal cortex slices. The peculiarities of the effects of lactate and pyruvate on the uptake were correlated with the partial divergence of the pathways of gluconeogenesis from these precursors. The linkage of the weak organic acid uptake with gluconeogenesis is interpreted in terms of the hypothesis that the uptake is controlled by the cytoplasmic pyridine nucleotide redox potential, which is maintained with the participation of certain processes involved in glucose synthesis.
我们使用糖异生抑制剂(苯丙酮酸、α-氰基-4-羟基肉桂酸、喹啉酸、D-苹果酸、氨氧基乙酸),分析了糖异生底物乳酸和丙酮酸以及短链脂肪酸乙酸盐刺激大鼠肾脏摄取弱有机酸荧光素的机制。我们已经表明,这些抑制剂改变了肾皮质片段悬浮液中由乳酸和丙酮酸生成葡萄糖的速率,以及代谢底物对肾皮质切片浅表近端小管中荧光素摄取的刺激作用。乳酸和丙酮酸对摄取的影响特点与这些前体物质糖异生途径的部分差异相关。弱有机酸摄取与糖异生之间的联系是根据以下假设来解释的:摄取受细胞质吡啶核苷酸氧化还原电位控制,而该电位通过参与葡萄糖合成的某些过程得以维持。