Nikiforov A A, Ostretsova I B
I. M. Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, M. Thorez pr. 44, 194223, St. Petersburg, Russia.
Ross Fiziol Zh Im I M Sechenova. 1997 May-Jun;83(5-6):165-89.
Stimulatory effects of intermediates of the tricarboxylic acid cycle on renal uptake of a weak organic anion, fluorescein, were studied with the aid of the method of contact microfluorimetry of individual convoluted proximal tubules ascending to the surface of the rat renal cortex slices. The study was undertaken for verifying the hypothesis that energization of renal excretion of anionic exenobiotics is mediated through their transport across the basolateral membrane in exchange for cytoplasmic alpha-ketoglutarate serving as a counter-anion. Effects of inhibitors of the tricarboxylic acid cycle such as fluoroacetate, malonate and 5-methoxyindole-2-carboxylate on the fluorescein uptake and renal gluconeogenesis in the presence of the metabolic substrates were investigated in order to outline metabolic pathways that could be responsible for elevation of the cytoplasmic alpha-ketoglutarate. Obtained data evidence that the stimulatory effects of the tricarboxylic acid cycle intermediates on the transport process under study depend on the metabolic state of the mitochondria and involve an activation of certain reactions but not the cycle as a whole. It has been suggested that an elevation of the cytoplasmic alpha-ketoglutarate resulting from this activation can be conditioned by export of isocitrate from the mitochondria with its subsequent transformation into alpha-ketoglutarate in the cytoplasm in the isocitrate dehydrogenase reaction.
借助对大鼠肾皮质切片表面上升的单个近曲小管进行接触式显微荧光测定法,研究了三羧酸循环中间产物对弱有机阴离子荧光素肾摄取的刺激作用。进行这项研究是为了验证以下假设:阴离子外源性物质经肾排泄的能量供应是通过它们跨基底外侧膜转运,以交换作为抗衡阴离子的细胞质α-酮戊二酸来介导的。研究了三羧酸循环抑制剂,如氟乙酸、丙二酸和5-甲氧基吲哚-2-羧酸酯在存在代谢底物的情况下对荧光素摄取和肾糖异生的影响,以便勾勒出可能导致细胞质α-酮戊二酸升高的代谢途径。获得的数据表明,三羧酸循环中间产物对所研究的转运过程的刺激作用取决于线粒体的代谢状态,并且涉及某些反应的激活,而不是整个循环的激活。有人提出,这种激活导致的细胞质α-酮戊二酸升高可能是由于异柠檬酸从线粒体中输出,随后在异柠檬酸脱氢酶反应中在细胞质中转化为α-酮戊二酸所致。