| Literature DB >> 7266681 |
Y Morot-Gaudry, S Bourgoin, M Hamon.
Abstract
Following an intravenous administration of 3H-tryptophan to mice, 3H-serotonin rapidly accumulated in the brain, with a maximum around the 20th min after the injection. In mice whole monoamine oxidase activity was blocked by pargyline (75 mg/kg i.p.), reserpine pretreatment (5 mg/kg, 24 h before death) did not alter the initial accumulation of 3H-5-HT indicating that the rate of 5 HT synthesis was similar in control and reserpinized animals. When monoamine oxidase was not blocked, the accumulation of 3H-5-HT was significantly lower in reserpine-treated mice than in controls. However, the specific activity of 3H-5-HT accumulated in brain was 2-3 times higher in reserpinized (45 h) than in control mice. Since neither the specific activity of the precursor 3H-tryptophan, the reuptake process for 3H-5-HT nor the absolute synthesis rate of 5-HT was altered in the brain of reserpinized mice, it is proposed that the differences observed in the specific activity of 3H-5-HT reflected the presence of 3H-5-HT in different compartments in control and reserpinized mice. Serotonin would be distributed in a "storage" and a "functional" compartments in serotoninergic neurons under normal conditions whereas only the functional compartment would exist 18-48 h after the administration of reserpine.Entities:
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Year: 1981 PMID: 7266681 DOI: 10.1007/BF00501363
Source DB: PubMed Journal: Naunyn Schmiedebergs Arch Pharmacol ISSN: 0028-1298 Impact factor: 3.000