Summary
A method for the chromatographic separation (Dowex 50 W, X-4) and fluorimetric determination of 3-methoxytyramine in brain tissue is described. The chromatographic procedure is an extension of the method for the separation of noradrenaline, dopamine and 5-hydroxytryptamine published by Atack and Magnusson (1970) and can be combined with that for monoamine precursors described by Kehr et al. (1972). 3-Methoxytyramine is eluted in N ethanolic (50%)-HCl and oxidized with potassium ferricyanide in ammonium hydroxide solution. Compared with previously published methods, the sensitivity is increased 2 to 5 fold. Reproducibility, recovery and specificity of the method are satisfactory. The level of 3-methoxytyramine found in normal rat brain is below the limit of sensitivity (10 ng/g). The amount of 3-methoxytyramine accumulating after inhibition of monoamine oxidase (MAO) differs depending on the inhibitor used. These differences in 3-methoxytyramine formation might be due to incomplete MAO inhibition, changes in dopamine synthesis, and releasing activity of the compounds investigated.
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Kehr, W. A method for the isolation and determination of 3-methoxytyramine in brain tissue. Naunyn-Schmiedeberg's Arch. Pharmacol. 284, 149–158 (1974). https://doi.org/10.1007/BF00501119
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DOI: https://doi.org/10.1007/BF00501119