A COMPARISON OF AN IMPROVED O‐PHTHALALDEHYDE FLUORO‐METRIC METHOD AND HIGH PRESSURE LIQUID CHROMATOGRAPHY IN THE DETERMINATION OF BRAIN 5‐HYDROXYINDOLES OF RATS TREATED WITH L‐TRYPTOPHAN AND p‐CHLOROPHENYL‐ALANINE
- 1 June 1981
- journal article
- research article
- Published by Wiley in British Journal of Pharmacology
- Vol. 73 (2) , 555-561
- https://doi.org/10.1111/j.1476-5381.1981.tb10455.x
Abstract
1 The determination of 5-hydroxytryptamine (5-HT) and 5-hydroxyindoleacetic acid (5-HIAA) by reaction with o-phthalaldehyde (OPT) in the presence of cysteine and subsequent fluorometry was compared with determination by a new high pressure liquid chromatography (h.p.l.c.) electrochemical method. 2 The methods were used to investigate a claim that the OPT method gives falsely high brain 5-HT values for rats given tryptophan (greater than 25 mg/kg i.p.) and as a consequence an inhibition of 5-HT synthesis by tryptophan is obscured. 3 High concentrations of tryptophan caused some increase of fluorescence when added to 5-HT solutions and carried through the OPT method, e.g. tryptophan (80 micrograms/ml) gave fluorescence identical to 5-HT (0.13 micrograms/ml). This interference was decreased by more than half and the sensitivity of the method increased if cysteine was added at more stages and fluorescence developed at 77 degrees C instead of 100 degrees C. 4 The h.p.l.c. and modified OPT methods did not give significantly different mean brain 5-HT or 5-HIAA values in rats given 0,25,100,250 mg/kg L-tryptophan though values were somewhat higher by the OPT method with the highest dose. This method gave significantly higher residual brain 5-HT values (12% of control) than did the h.p.l.c. method (8% of control) after inhibiting 5-HT synthesis by p-chlorophenylalanine (150 mg/kg X 3). 5 There was no indication that tryptophan inhibited 5-HT synthesis even when brain tryptophan was increased about 30 fold (from 3.8 to 124 micrograms/g). 6 Results confirm the general reliability of the OPT method although h.p.l.c. has some advantages i.e. separation of 5-hydroxyindoles from tryptophan, greater sensitivity, ease of automation.Keywords
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