OCTOPAMINE IN MAMMALIAN BRAIN: RAPID POST MORTEM INCREASE AND EFFECTS OF DRUGS

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Abstract
—: A modified enzyme radiochemical assay for octopamine, based upon the N‐methylation of octopamine by the enzyme phenylethanolamine N‐methyl transferase (S‐Adenosyl‐1‐methionine: phenylcthanolamine N‐methyl transferase EC 2.1.28), has been developed. [3H]Methyl‐S‐adenosyl‐l‐ methionine was used as methyl donor, and the reaction products separated by thin‐layer chromatography prior to liquid scintillation counting. The method had a sensitivity of about 100 pg, and was suitable for the measurement of endogenous octopamine levels in mammalian brain. Although the method could be used for the determination of phenylethanolamine with similar sensitivity, concentrations of this amine in brain were too low for routine measurement. Octopamine levels in the brains of a number of mammalian species were determined using this procedure. Concentrations of the amine in mouse brain were lower in animals killed by rapid freczing than in animals killed by decapitation; a further increase in brain octopamine took place post‐mortem. Brain octopamine was increased following treatment with MAO inhibitors, p‐chlorophenylalanine, phenylalanine, tyrosine or phenylethylamine. The effects of tyrosine and phenylethylamine were greatly increased by pretreatment with a monoamine oxidase inhibitor. The antidepressants imipramine and iprindole gave rise to increased brain octopamine concentrations, possibly through an effect upon monoamine oxidase. Administration of chlordiazepoxide chlorpromazine, thyroxine, or reserpine had no effect upon brain octopamine.