BRAIN AND PERIPHERAL METABOLISM OF 5-HYDROXYTRYPTOPHAN-C-14 FOLLOWING PERIPHERAL DECARBOXYLASE INHIBITION

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  • 1 January 1976
    • journal article
    • research article
    • Vol. 197  (3) , 545-555
Abstract
Following selective peripheral decarboxylase inhibition, a greater fraction of peripherally measured monoamine metabolites should derive from CNS monoamine metabolism. In rats pretreated with the peripheral decarboxylase inhibitor L-.alpha.-(3,4-dihydroxybenzyl)-.alpha.-hydrazinopropionic acid (MK-486) (50 mg/kg i.p. or i.v.), the peripheral formation of 5-hydroxytryptamine-14C (5-HT-14C) from the precursor DL-5-hydroxytryptophan-14C (5-HTP-14C) was reduced by 82-100% over a 4 h interval. There was a marked increase in the penetration of 5-HTP-14C into brain and in the appearance in brain of 5-HT-14C and 5-hydroxyindoleacetic acid-14C (5-HIAA-14C). The cerebral metabolism of 5-HTP-14C in vehicle-pretreated animals appeared to occur mainly in the brain vascular compartment. Following MK-486 pretreatment, the in vivo metabolism of 14C-5-hydroxyindoles in the extracerebral compartment obeys linear kinetics as does the uptake and decarboxylation of 5-HTP-14C in brain. The cerebral turnover of 5-HT-14C appeared to increase as a function of the dose of 5-HTP injected. This phenomenon may be a result of either saturation of brain 5-HT storage sites or nonspecific metabolism of 5-HTP in brain catecholamine neurons. A highly significant correlation was found between the brain and blood 5-HIAA-14C levels following MK-486. The adrenal formation of 5-HT, which was not inhibited by MK-486, did not appear to contribute significantly to the blood 5-HIAA-14C levels. The possibility that following peripheral decarboxylase inhibition a larger fraction of peripherally measured 5-HIAA may derive from CNS 5-HT metabolism is suggested.