Metabolism of C¹⁴-labeled substrates by rabbit kidney cortex and medulla

¹ Department of Medicine, Harvard Medical School, and Peter Bent Brigham Hospital, Boston, Massachusetts

Slices of rabbit kidney cortex and medulla were incubated for 90 min at 38 C in Krebs-Ringer bicarbonate buffer containing C¹⁴ labeled substrate. In addition to substrate disappearance and concentrations of glycogen and fatty acids, measurements were made of the amount of radioactive substrate incorporated into CO₂, glycogen, and fatty acids per gram of wet tissue. Glucose, fructose, mannose, glycerol, pyruvate, and palmitate were oxidized to a significantly greater extent by cortex than medulla. The concentration of glycogen in kidney medulla was twice that of cortex and was maintained at initial concentrations only in the presence of glucose, which showed a significantly greater incorporation into medullary glycogen than did the other substrates. Under pure anaerobic conditions simulating those in vivo, the present study suggests that the metabolism of medulla is almost exclusively glucose-dependent anaerobic glycolysis. On the other hand, the cortex is capable of utilizing a variety of substrates for a high rate of aerobic metabolism.

Note:
With the Technical Assistance of Beatrix Küffer

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