Determination of Normetanephrine, 3,4‐Dihydroxyphenylethyleneglycol (Free and Total), and 3‐Methoxy‐4‐Hydroxyphenylethyleneglycol (Free and Total) in Rat Brain by High‐Performance Liquid Chromatography with Electrochemical Detection and Effects of Drugs on Regional Concentrations
- 1 April 1984
- journal article
- research article
- Published by Wiley in Journal of Neurochemistry
- Vol. 42 (4) , 934-942
- https://doi.org/10.1111/j.1471-4159.1984.tb12694.x
Abstract
A new, fast and sensitivity assay for normetanephrine (NM), free and total 3,4-dihydroxyphenylethyleneglycol (DOPEG), and free and total 3-methoxy-4-hydroxyphenylethyleneglycol (MOPEG) in brain tissue is described. The method is based on high-performance liquid chromatography with electrochemical detection. Small Sephadex G 10 columns were used for prepurification. This permitted the additional isolation and quantification of tyrosine, 3,4-dopa, noradrenaline [norepinephrine (NA)] dopamine, 3-methoxytyramine, 3,4-dihydroxyphenylacetic acid, homovanillic acid, and 5-hydroxyindoleacetic acid. The compounds were determined in 6 brain areas (striatum, cortex, hippocampus, hypothalamus, brainstem, and cerebellum). Most DOPEG and MOPEG in rat brain was present in the conjugated form, except for the cerebellum, where about 80% of MOPEG was nonconjugated. No postmortem effects on MOPEG levels were observed; a slight increase in DOPEG in certain brain areas was found in microwave-killed rats. The effects of clonidine, yohimbine, N,N-dipropyl-5,6-ADTN [aminodihydrotetrahydronaphthalene] and chlorpromazine on the concentrations of the 5 N metabolites were determined. Free and total DOPEG and MOPEG provide similar information on NA metabolism, whereas NM (after monoamine oxidase inhibition) reflects a different type of interaction of drugs with NA metabolism. The similarity in the pattern of drug-induced changes in NA metabolism in the various brain areas suggests that adrenoreceptors mediating NA metabolism are homogeneously distributed throughout the brain.Keywords
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