Platelet phenol sulfotransferase and erythrocyte catechol-O-methytransferase activities: Correlation with methyldopa metabolism

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Abstract
Methyldopa [an antihypertensive drug] is metabolized by sulfate conjugation catalyzed by phenol sulfotransferase (PST), O-methylation catalyzed by catechol-O-methyltransferase (COMT) and decarboxylation catalyzed by aromatic L-amino acid decarboxylase. Whether individual variations in red blood cell (RBC) COMT and platelet PST activities might reflect variations in the metabolism of methyldopa in man were determined. Methyldopa, 3.5 mg/kg, was taken orally by 28 subjects. Blood samples were obtained from these subjects for the assay of platelet PST and RBC COMT activities, and a 24-h urine sample was collected for the measurement of methyldopa and its major metabolites. Human platelets contain 2 independently regulated forms of PST. One form is thermolabile (TL), and the other is thermostable (TS). Methyldopa and .alpha.-methyldopamine are substrates for the TL but not for the TS form of PST. Significant correlation exist between TL platelet PST activity and the proportion of .alpha.-methyldopamine excreted as a sulfate conjugate, and between RBC COMT activity and the proportion of methyldopa excreted as an O-methyl metabolite. There was no significant correlation between TL platelet PST activity, and the proportion of methyldopa itself excreted as a sulfate conjugate. Differences among subjects in drug metabolizing enzyme activities are evidently one factor responsible for wide individual variations in methyldopa metabolism in man.