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

Abstract

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.