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Tetrahydrobiopterin (BI-L) is the cofactor for the pteridine-de~ndent monoxygenases (phenylalanine tyrosine and tryptophan hydroxylases) (Kaufmann and Fisher 1974), which play important roles in the biosynthesis of biogenic amines such as catecholamines and indolamines. The biosynthesis of these biogenic amines is regulated by the hydroxylat~on reaction of amino acids such as tyrosine and tryptophan (Nagatsu et al. 1964; Lovenberg et al. 1967), and this hydroxylation reaction is regulated by the concentration of BH4 (Kettler et ~J. !974). These biogenic amines, especially noradrenaliE.e and serotonin, have been thought to be related to affective disorders (Van Praag 1982). Therefore, the relationship between BH4 and depression has been of particular interest, and some controversial results about this relationship have been reported: lowering of the BI-L~ synthesi,~ in the postmortem brains of patients with depression (Blair et al. 1984); no difference between the CSF biopterin levels in patients with depression and in normal controls (Kellner et al. 1980; Levine and Lovenberg 1984); an in

Monoamine oxidase (MAO) is a mitochondrial enzyme responsible for the oxidative deamination of catecholamines and indolamines (Alexopoulos et al 1984). Plate!ets contain only MAO-B, whereas human brain contains both MAO-A and MAO-B (Po~,rier et al 1987). The kinetics of platelet MAO-B are believed to be similar to central turnover of monoamines (Georgotas et al 1986), but Young and colleagues (1986) found no connection between platelet and brain MAO-B. Nevertheless, this controversial area has been implicated in attempts to identify a biological marker tbr the evaluation of the size or capacity of the central serotonin system (Hailman et al 1990). In this study we examined platetet MAO-B activity as a biological marker tbr depressive and anxiety disorders, giving par.icular attention to its relation to age of onset.