METABOLISM OF MALONIC ACID IN RAT BRAIN AFTER INTRACEREBRAL INJECTION

— Labeled malonic acid ([1‐ 14 C] and [2‐ 14 C]) was injected into the left cerebral hemisphere of anesthetized adult rats in order to determine the metabolic fate of this dicarboxylic acid in central nervous tissue. The animals were allowed to survive for 2, 5, 10. 15 or 30min. Blood was sampled from the torcular during the experimental period and labeled metabolites were extracted from the brain after intracardiac perfusion. There was a very rapid efflux of unreacted malonate in the cerebral venous blood. Labeled CO 2 was recovered from the venous blood and the respired air after the injection of [1‐ 14 C]malonate but not after [2‐ 14 C]malonate. The tissue extracts prepared from the brain showed only minimal labeling of fatty acids and sterols. Much higher radioactivity was present in glutamate, glutamine, aspartate, and GABA. The relative specific activities (RSA) of glutamine never rose above 1.00. Aspartate was labeled very rapidly and revealed evidence of 14 CO 2 fixation in addition to labeling through the Krebs cycle. GABA revealed higher RSA after [1‐ 14 C]malonate than after [2‐ 14 C]malonate. Sequential degradations of glutamate and aspartate proved that labeling of these amino acids occurred from [1‐ 14 C] acetyl‐CoA and [2‐ 14 C] acetyl‐CoA, respectively, via the Krebs cycle. Malonate activation and malonyl‐CoA decarboxylation in vivo were similar to experiments with isolated mitochondria. However, labeled malonate was not incorporated into the amino acids of free mitochondria. The results were compared to data obtained after intracerebral injection of [1‐ 14 C]acetate and [2‐ 14 C]acetate.