In vivo metabolism of serotonin and tryptamine: effect of monoamine oxidase inhibition.
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Biomedical subjects
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alpha-Methyl-3,4-dihydroxy-DLphenylalanine has been found to be an effective inhibitor of aromatic amino acid decarboxylation in man. This was shown by decreased formation of serotonin, tryptamine, and tyramine from the precursor amino acids. Reduction of amine biosynthesis is associated with lowering of blood pressure in hypertensive patients and a transient sedative effect.
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The administration of monoamine oxidase inhibitors produces an increase in the urinary excretion of many amines for which efficient alternate routes of metabolism are not available. These include tryptamine, paratyramine, and a "metatyramine-like" substance. The inhibitors can therefore be used to detect previously unsuspected pathways of amino acid decarboxylation. The finding that the excretions of norepinephrine, epinephrine, 3,4-dihydroxyphenylethylamine, and possible serotonin are not appreciably affected are consistent with previous reports of the existence of alternative metabolic routes.
The administration of ketoproline to chick embryos resulted in an increase in the free hydroxyproline. This phenomenon is explained by the inhibitory action of ketoproline on the catabolism of hydroxyproline as well as by the conversion of the former to the latter. Ketoproline was found to be reduced to hydroxyproline by the supernatant fraction of rat-kidney homogenate in the presence of a reduced pyridine nucleotide.
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