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Journal of Pharmacology And Experimental Therapeutics, Vol. 153, Issue 2, 183-190, 1966
Copyright © 1966 by American Society for Pharmacology and Experimental Therapeutics


THE METABOLISM OF TYRAMINE IN RABBITS

L. Lemberger 1, A. Klutch 1, and R. Kuntzman 1

1 The Wellcome Research Laboratories, Tuckahoe, New York, and Department of Pharmacology, Albert Einstein College of Medicine, New York, New York

The urinary excretion of radioactive metabolites has been qualitatively and quantitatively investigated in rabbits after the intraperitoneal administration of tyramine-C14. The major urinary metabolite found was p-hydroxy-phenylacetic acid, which accounted for approximately 85% of the urinary radioactivity. Three other metabolites, 3-methoxy-4-hydroxymandelic acid (VMA), homovanillic acid (HVA) and p-hydroxymandelic acid (p-HMA), which have not previously been found in urine after tyramine administration, have been identified. In addition, p-hydroxyphenylethyl alcohol and two unidentified metabolites were found. The presence of radioactive catecholamine metabolites (i.e., HVA and VMA) indicates that tyramine can be converted in vivo to catecholamines. The finding of p-HMA provides further evidence for the in vivo conversion of tyramine to octopamine. The significance and implications of these metabolic pathways are discussed.

Accepted on March 1, 1966




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A. Okina, S. Hidaka, M. Tashiro, and K. Abe
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Copyright © 1966 by the American Society for Pharmacology and Experimental Therapeutics.