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Abstract
Using a rapid, quantitative high pressure liquid chromatographic (HPLC) procedure for the separation of S-adenosyl-L-homocysteine (AdoHcy) and its purinic metabolites in rat and mouse brain, kidney and liver, we found that uric acid is the principal catabolic product of AdoHcy metabolism in the liver, but that none forms in brain. Rat kidney formed about 10 times as much uric acid and half as much hypoxanthine as did mouse kidney. The HPLC procedure has been adapted to assay AdoHcy hydrolase activity which was found to be lowest in the brain and highest in the liver.
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