Summary: A population of cerebrovascular nerve fibers have recently been found to store serotonin (5-hydroxy tryptamine; 5-HT). There is reason to assume that these 5-HT-containing fibers have a sympathetic rather than an intracerebral origin. This was further elucidated in the present study in which the uptake mechanisms of 5-HT and noradrenaline ( N A) were characterized and com pared in rat pial arteries by measuring the accumulation of , 1984). Since the early report by Nielsen and Owman (1967) on the presence of an extensive supply of sympathetic nerve terminals in cerebral arteries, a wide range of neurotransmitter amines an d peptides have been discovered in nerves asso ciated with brain vessels (Owman et aI., 1986). Among these, serotonin (5-hydroxytryptamine; 5-HT) has attracted special attention since it was re cently found that the indole is present in cerebro vascular nerve fibers of different species (Griffith et aI., 1982;Griffith and Burnstock, 1983; Edvinsson et aI., 1983 Edvinsson et aI., , 1984Chang and Owman, 1986; Cowen et aI., 1986 Cowen et aI., , 1987.Received November 28, 1988; revised July 17, 1989; accepted July 21, 1989.Address correspondence and reprint requests to Prof. Ch. Owman at Department of Medical Cell Research, Biskopsgatan 5, S-223 62 Lund, Sweden.Abbreviations used: 5-HIAA, 5-hydroxyindoleacetic acid; 5-HT, 5-hydroxytryptamine; NA, noradrenaline.
22amine. Corticosterone, acting on the extraneuronal pro cess, significantly inhibited the 5-HT uptake but had no substantial effect on NA. Reserpine, blocking the intraax onal vesicular stores, markedly attenuated the accumula tion ofNA, but not of 5-HT. The selective uptake blocker paroxetine reduced the 5-HT uptake with much higher potency than the NA uptake, whereas desipramine pre dominantly inhibited NA uptake. The pial 5-HT uptake was not significantly affected by lesion of the raphe com plex, whereas it was reduced to half following superior cervical ganglionectomy. The results suggest that the 5-HT present in nerves associated with pial vessels at the base of the brain is taken up through an efficient axonal mechanism, functionally related but not identical to the uptake process for NA.